The application of activated carbon for the adsorption and elution of platinum group metals from dilute cyanide leach solutions

The research presented in this paper investigated the practical aspects of the recovery of platinum group metals (PGMs) from a dilute cyanide leach solution containing base metals, in a manner similar to that used for gold extraction in a typical CIP process, and focuses on both the adsorption and elution stages. The carrier phase extraction of precious metals using activated carbon offers significant advantages over other processes in terms of simplicity, the high pre-concentration factor, rapid phase separation, and relatively low capital and operating costs. As a sorbent, activated carbon is still by far the most important material because of its large surface area, high adsorption capacity, porous structure, negligible environmental toxicity, low cost, and high purity standards. Adsorption tests were conducted on a pregnant alkaline leach solution (0.15 ppm Pt, 0.38 ppm Pd, 0.1 ppm Au) resulting from cyanide extraction performed in column leach tests. The initial adsorption rates of Pt, Pd, and Au were very fast and recoveries of these three metals were approximately 90 per cent after 2 hours, and 100 per cent for Pt, 97.4 per cent for Pd, and 99.9 per cent for Au after 72 hours. The parameters that influence the extraction of PGMs and Au were examined to assess their relative importance during the adsorption process in order to provide the basis for process optimization. The concentration of thiocyanate was not identified as significant factor for PGMs adsorption, while Ni concentration was the most significant extraction process parameter. Base metal cyanide complexes adsorb and compete with the PGM complexes for sites on activated carbon, and while copper adsorption can be minimized by adjusting the residence time, Ni adsorbs at approximately the same rate as the PGMs, influencing the loading capacity and adsorption kinetics of the PGMs.The feasibility of eluting platinum and palladium cyanide complexes from activated carbon using an analogue of the AARL process was investigated. Platinum and palladium elute from activated carbon almost to completion in 4 to 5 bed volumes at 80°C, while the elution of gold at this temperature is slow, with a significant amount of gold still to be eluted after 16 bed volumes. The equilibrium loading of gold is exothermic in nature (Fleming and Nicol, 1984) which will result in an increase in gold elution kinetics with an increase in temperature at similar pre-treatment conditions. A similar result was found for the elution of Pt and Pd. Cyanide pre-treatment was found to have a significant influence on PGM elution. Higher cyanide concentration in the pre-treatment step results in more efficient elution up to a point, and results suggest the possibility of an optimum cyanide concentration, beyond which elution efficiency starts decreasing due to increased ionic strength

The Adsorption and Elution of Platinum Group Metals (Pt, Pd, and Au) from Cyanide Leach Solutions using Activated Carbon

This paper investigates the recovery of platinum group metals (PGMs) from a dilute cyanide leach solution containing base metals, in a manner similar to that used for gold extraction in a typical CIP process, and focuses on both the adsorption and elution stages. The carrier-phase extraction of precious metals using activated carbon offers significant advantages over other processes in terms of simplicity, the high pre-concentration factor, rapid phase separation, and relatively low capital and operating costs. As a sorbent, activated carbon is still by far the most important material because of its large surface area, high adsorption capacity, porous structure, negligible environmental toxicity, low cost, and high purity standards. Adsorption tests were performed on a pregnant alkaline leach solution (0.15 ppm Pt, 0.38 ppm Pd, 0.1 ppm Au) resulting from cyanide extraction performed in column leach tests. The initial adsorption rates of platinum, palladium, and gold were very fast and recoveries of these three metals were approximately 90 per cent after 2 hours and 100 per cent, 97.4 per cent, and 99.9 per cent respectively after 72 hours. The parameters that influence the extraction of PGMs and Au were examined to assess their relative importance during the adsorption process in order to provide the basis for process optimization. The concentration of thiocyanate was not identified as significant factor for PGMs adsorption, while nickel concentration was the most significant extraction process parameter. Base metal cyanide complexes adsorb and compete with the PGM complexes for sites on activated carbon, and while copper adsorption can be minimized by adjusting the residence time, nickel adsorbs at approximately the same rate as that of the PGMs, influencing the loading capacity and adsorption kinetics of the PGMs.The feasibility of eluting platinum and palladium cyanide complexes from activated carbon using an analogue of the AARL process was investigated. Platinum and palladium elute from activated carbon almost to completion in 4 to 5 bed volumes at 80°C, while the elution of gold at this temperature is slow, with a significant amount of gold still to be eluted after 16 bed volumes. Cyanide pre-treatment was found to have a significant influence on PGM elution. Higher cyanide concentration in the pre-treatment step results in more efficient elution up to a point, and experiments suggest the possibility of an optimum cyanide concentration, beyond which elution efficiency starts decreasing

Investigation of flow regime transition in a column flotation cell using CFD

Flotation columns are normally operated at optimal superficial gas velocities to maintain bubbly flow conditions. However, with increasing superficial gas velocity, loss of bubbly flow may occur with adverse effects on column performance. It is therefore important to identify the maximum superficial gas velocity above which loss of bubbly flow occurs. The maximum superficial gas velocity is usually obtained from a gas holdup versus superficial gas velocity plot in which the linear portion of the graph represents bubbly flow while deviation from the linear relationship indicates a change from the bubbly flow to the churn-turbulent regime. However, this method is difficult to use when the transition from bubbly flow to churn-turbulent flow is gradual, as happens in the presence of frothers. We present two alternative methods in which the flow regime in the column is distinguished by means of radial gas holdup profiles and gas holdup versus time graphs obtained from CFD simulations. Bubbly flow was characterized by saddle-shaped profiles with three distinct peaks, or saddle-shaped profiles with two near-wall peaks and a central minimum, or flat profiles with intermediate features between saddle and parabolic gas holdup profiles. The transition regime was gradual and characterized by flat to parabolic gas holdup profiles that become steeper with increasing superficial gas velocity. The churn-turbulent flow was distinguished by steep parabolic radial gas holdup profiles. Gas holdup versus time graphs were also used to define flow regimes with a constant gas holdup indicating bubbly flow, while wide gas holdup variations indicate churn-turbulent flow

Cancellation and error correction for narrowband interference with spectral nulls codes and OFDM modulation

Conference proceeding

Error correction of frequency-selective fading channels with spectral nulls codes

Abstract: In this paper, we investigate a prior error correction technique for frequency selective fading channels. Spectral nulls codes with nulls at submultiple frequencies are used to avoid fades at the corresponding frequencies. Coincide the spectrum null at the corresponding fading frequency and playing with its wideness, will minimize the bit errors caused by the channel

The selectivity filter is involved in the U-type inactivation process of Kv2.1 and Kv3.1 channels

Voltage-gated potassium (Kv) channels display several types of inactivation processes, including N-, C-, and U-types. C-type inactivation is attributed to a nonconductive conformation of the selectivity filter (SF). It has been proposed that the activation gate and the channel's SF are allosterically coupled because the conformational changes of the former affect the structure of the latter and vice versa. The second threonine of the SF signature sequence (e.g., TTVGYG) has been proven to be essential for this allosteric coupling. To further study the role of the SF in U-type inactivation, we substituted the second threonine of the TTVGYG sequence by an alanine in the hKv2.1 and hKv3.1 channels, which are known to display U-type inactivation. Both hKv2.1-T377A and hKv3.1-T400A yielded channels that were resistant to inactivation, and as a result, they displayed noninactivating currents upon channel opening; i.e., hKv2.1-T377A and hKv3.1-T400A remained fully conductive upon prolonged moderate depolarizations, whereas in wild-type hKv2.1 and hKv3.1, the current amplitude typically reduces because of U-type inactivation. Interestingly, increasing the extracellular K+ concentration increased the macroscopic current amplitude of both hKv2.1-T377A and hKv3.1-T400A, which is similar to the response of the homologous T to A mutation in Shaker and hKv1.5 channels that display C-type inactivation. Our data support an important role for the second threonine of the SF signature sequence in the U-type inactivation gating of hKv2.1 and hKv3.1. SIGNIFICANCE Voltage-dependent K+ (Kv) channels generate cells' repolarizing power, which is consequently regulated by the channel's conductance. Aside from the opening or closure, Kv channels undergo inactivation that drives them into a lower or nonconductive state. Among the different inactivation processes described in Kv channels, the U-type process develops from a preopen but activated state. The molecular determinants of this process are, in contrast to the Ctype mechanism, not well characterized. Our data show that the intracellular part of the K+ selectivity filter within the pore domain is involved. An alanine for threonine substitution results in channels that do not inactivate upon opening, suggesting that an allosteric coupling between the activation gate and selectivity filter exists in U-type inactivation

Investigating the behaviour of PGEs during first-stage leaching of a Ni-Fe-Cu-S converter matte

CITATION: Snyders, C. A., et al. 2018. Investigating the behaviour of PGEs during first-stage leaching of a Ni-Fe-Cu-S converter matte. Journal of the Southern African Institute of Mining and Metallurgy, 118(4):353-360, doi:10.17159/2411-9717/2018/v118n4a4.The original publication is available at http://www.scielo.org.zaENGLISH ABSTRACT: In a first-stage atmospheric leach in a Sherritt Ni-Cu matte leach process, a Ni-Cu-Fe-S Peirce-Smith converter matte is contacted with recycled aqueous copper sulphate/sulphuric acid solution (spent solution) with the purpose of dissolving nickel, while simultaneously removing copper (via metathesis and cementation reactions) from solution. While the iron content has been found to have a significant impact on the first-stage leach, a previously expected relationship between copper and PGM behaviour has not been established clearly. For this study, a converter matte consisting mainly of heazlewoodite (Ni3S2), chalcocite (Cu2S), and awaruite (Ni3Fe) was leached in a laboratory-scale batch reactor. The temperature, acid, and copper concentration under both oxidative and non-oxidative conditions were varied, while the copper, iron, and PGEs were tracked and the pH and Eh measured. Palladium was generally found to be closely related to the behaviour of copper, while platinum did not leach. The other platinum group metals such as iridium and rhodium were found to precipitate only with accelerated precipitation being observed during Fe precipitation reactions.http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S2225-62532018000400007Publisher's versio

Combined spectral shaping codes and OFDM modulation for narrowband interference channels

Abstract: Distance Preserving Mappings is a relatively new technique finding its way to a wide use in the coding field. New codes mapping convolutional code outputs onto spectral nulls codewords have the purpose of generating a code with a certain spectrum specification and error correction capabilities, which can be exploited by the Viterbi decoder. Combining this class of new codes with an Orthogonal Frequency Division Multiplexing modulation scheme is actually a tool to reduce Electromagnetic Compatibility Interference in selected subbands or to cancel the narrowband interference potentially caused by, amongst others, high frequency radio transmissions. Taking into consideration the fact that a narrowband noise source is almost similar to a modulated orthogonal frequency division multiplexing carrier, and also the periodicity of the nulls in our spectrum, we are able to cancel the narrowband signal and its sideband interferences without using traditional techniques of cancellation, which is based on filtering. Shaping our spectrum at the transmitter is a technique, which can be exploited at the receiver to suppress any narrowband signal interference, which is regarded as noise. We will present in this paper the technique of cancellation and the coding gain that can be obtained when comparing to the uncoded data

Platinum and palladium on carbon nanotubes:Experimental and theoretical studies

<p>Pristine and oxygen plasma functionalised carbon nanotubes (CNTs) were studied after the evaporation of Pt and Pd atoms. High resolution transmission electron microscopy shows the formation of metal nanoparticles at the CNT surface. Oxygen functional groups grafted by the plasma functionalization act as nucleation sites for metal nanoparticles. Analysis of the C1s core level spectra reveals that there is no covalent bonding between the Pt or Pd atoms and the CNT surface. Unlike other transition metals such as titanium and copper, neither Pd nor Pt show strong oxygen interaction or surface oxygen scavenging behaviour. (C) 2013 Elsevier B.V. All rights reserved.</p>