The Uptake Characteristics of Prussian-Blue Nanoparticles for Platinum-Group Metal and Molybdenum Ions in a Nitric Acid Solution Toward Application for the Recovery of Precious Metals from Nuclear and Electronic Wastes

We have examined the uptake mechanisms of platinum-group-metals (PGMs) and molybdenum (Mo) ions into PBNPs in a nitric acid solution for 24-h sorption test, using inductively coupled plasma atomic emission spectroscopy, powder XRD, and UV-Vis-NIR spectroscopy in combination with first-principles calculations, and revealed that the Ru4+ and Pd2+ ions are incorporated into PBNPs by substitution with Fe3+ and Fe2+ ions of the PB framework, respectively, whereas the Rh3+ ion is incorporated into PBNPs by substitution mainly with Fe3+ and minorly with Fe2+ ion, and Mo6+ ion is incorporated into PBNPs by substitution with both Fe2+ and Fe3+ ions, with maintaining the crystal structure before and after the sorption test. Assuming that the amount of Fe elusion is equal to that of PGMs/Mo substitution, the substitution efficiency is estimated to be 39.0% for Ru, 47.8% for Rh, 87% for Pd, and 17.1% for Mo6+. This implies that 0.13 g of Ru, 0.16 g of Rh, 0.30 g of Pd, and 0.107 g of Mo can be recovered by using 1g PBNPs with a chemical form of KFe(III)[Fe(II)(CN)6].

One-pot synthesis of Au-based nanocrystals via a platinum group metal anions controlled growth strategy in citrate medium

The platinum group metals (PGM, Pd, Pt, Ir, etc.) possess unique chemical and physical properties, the properties often vary dramatically with their size, morphology, crystal structure, phase and composition. However,...

Variation in Platinum group metals determination using ICP OES induced by the effect of complex matrices and the correction method based on multivariate calibration

The presence of interelements due to sample complexity can produce significant effects on the quantitative determination of Platinum group metals (PGMs) by using inductively coupled plasma optical emission spectrometry (ICP...

Liquid-liquid extraction of Pt(IV) from hydrochloric acid solutions using PPG 425 – NaCl – H2O system

Today, metal extraction from e-waste is beneficial from both an environmental and economic point of view. Natural resources of metals, especially platinum group metals, are limited. At the same time, the amount of waste containing many valuable elements continues to grow. In this work, we studied the extraction of Pt (IV) from hydrochloric acid solutions using polypropylene glycol 425 (PPG 425). In the course of the experimental work, the dependence of the platinum extraction degree on the influence of hydrochloric acid concentration and medium pH in the polypropylene glycol 425 - sodium chloride - water system have been established. The maximum recovery (distribution coefficient > 3,5) has been achieved in the presence of 2 M HCl in an aqueous two-phase system (ATPS), which allows the use of the proposed system for the extraction of platinum from leaching solutions.

Selective determination of rhodium and iridium in the urban environment using the catalytic method

The problem of studying the level of technogenic pollution of the environment with platinum group metals is attributed first to the release of platinum metals into the environment together with the exhaust gases of cars using afterburning catalysts containing Pt, Pd, Rh. The pharmaceutical, electronics and jewelry industries the waste of which contains PGMs also contribute to the pollution of the environment. A number of studies have shown the toxic effects of PGM on humans. The goal of the study is to obtain new information about the level of technogenic pollution of the environment with platinum group metals (such as water-washings from roads, bio-collector plants, roadside dust), which necessitates developing of the method for sample preparation and determination of rhodium and iridium. A technique of sample opening and determination of rhodium and iridium in environmental objects, water-washings from roads, bio-collector plants, roadside dust is proposed. To increase the selectivity of rhodium determination, the samples were treated with a mixture of concentrated perchloric acid and sodium periodate when heated to boiling, which provided more than 5-fold increase the rhodium signal. Moreover, the permissible excess of iridium and ruthenium was increased by 5 and 20 times, respectively, due to the conversion of other PGMs into catalytically inactive forms. The indicator reaction of sulfarsazen oxidation by periodate was used in the kinetic determination of rhodium and iridium. The correctness of the results obtained by the developed method was confirmed by the ETAAS method. The determined content of Rh and Ir: in roadside waters (μg/liter) up to 0.015 and 0.005; in collector plants (g/ton) up to 0.030 Rh and 0.022; in street dust (g/ton) up to 0.05 and 0.025, respectively. The standard deviation of the repeatability of the determination results does not exceed 0.07 (Rh) and 0.12 (Ir). The developed method of opening samples and determining rhodium and iridium in environmental objects provided a great bulk of information about the content of rhodium and iridium in water-flushes from Moscow roads, bio-collector plants, roadside dust, which correlate fairly well with the scarce data from other geographic regions available in the literature and our earlier results on rhodium content in dust. The developed technique made it possible to obtain data on the level of technical pollution of the environment with PGMs in places with different traffic density in Moscow.