Selective formation of copper nanoparticles from acid mine drainage using nanoscale zerovalent iron particles

Nanoscale zerovalent iron (nZVI) has been investigated for the selective formation of Cu nanoparticles from acid mine drainage (AMD) taken from a legacy mine site in the UK. Batch experiments were conducted containing unbuffered (pH 2.67 at t=0) and pH buffered (pH 99.9% removal of all metals within 1 h when nZVI ≥1.0 g/L) from unbuffered AMD despite the coexistent of numerous other metals in the AMD, namely: Na, Ca, Mg, K, Mn and Zn. An acidic pH buffer enabled similarly high Cu removal but maximum removal of only <1.5% and <0.5% Cd and Al respectively. HRTEM-EDS confirmed the formation of discrete spherical nanoparticles comprised of up to 68% wt. Cu, with a relatively narrow size distribution (typically 20-100 nm diameter). XPS confirmed such nanoparticles as containing Cu0 , with the Cu removal mechanism therefore likely via cementation with Fe0 . Overall the results demonstrate nZVI as effective for the one-pot and selective formation of Cu0 -bearing nanoparticles from acidic wastewater, with the technique therefore potentially highly useful for the selective upcycling of dissolved Cu in wastewater into high value nanomaterials

Sorption and fractionation of rare earth element ions onto nanoscale zerovalent iron particles

The removal behaviour of rare earth element (REE), (Sc, Y, La-Lu), ions onto nanoscale zerovalent iron (nZVI) particles has been investigated. Batch sorption isotherms were conducted using REE-bearing acid mine drainage (AMD) and a range of different synthetic REE solutions, which were exposed to nZVI at 0.1-4.0 g/L. Maximum adsorption capacity of Yb and La was 410 and 61 mg/g respectively (1000 mg/L LaCl3 and YbCl3 starting concentration, initial pH=4.5, T=294 K), the highest currently reported in the literature. Aqueous REE removal to ultratrace concentrations (99.9% removal) was also recorded after 30 min (the first sampling interval) exposure of ≥0.5 g/L nZVI to 10 mg/L aqueous REE solutions (nitrate counterion). Similar rapidity and near-total removal ability was recorded for the exposure of nZVI to the AMD, however, a greater nZVI concentration was required, with the removal of all REEs (with the exception of La, Ce, Nd and Gd) to <1 µg/L when exposed to nZVI at 4.0g/L for 30 mins. In all systems nZVI was selective for the removal of HREE ions in preference to LREE ions, with the mechanism determined using HRTEM-EDS and XPS analysis as via surface mediated precipitation. Overall the results demonstrate nZVI as exhibiting great promise as an effective and versatile agent for simultaneous REE ion recovery and fractionation

Towards 'Precision Mining' of wastewater: Selective recovery of Cu from acid mine drainage onto diatomite supported nanoscale zerovalent iron particles

This paper introduces the concept of ‘Precision Mining’ of metals which can be defined as a process for the selective in situ uptake of a metal from a material or media, with subsequent retrieval and recovery of the target metal. In order to demonstrate this concept nanoscale zerovalent iron (nZVI) was loaded onto diatomaceous earth (DE) and tested for the selective uptake of Cu from acid mine drainage (AMD) and subsequent release. Batch experiments were conducted using the AMD and nZVI-DE at 4.0–16.0 g/L. Results demonstrate nZVI-DE as highly selective for Cu removal with >99% uptake recorded after 0.25 h when using nZVI-DE concentrations ≥12.0 g/L, despite appreciable concentrations of numerous other metals in the AMD, namely: Co, Ni, Mn and Zn. Cu uptake was maintained in excess of 4 and 24 h when using nZVI-DE concentrations of 12.0 and 16.0 g/L respectively. Near-total Cu release from the nZVI-DE was then recorded and attributed to the depletion of the nZVI component and the subsequent Eh, DO and pH recovery. This novel Cu uptake and release mechanism, once appropriately engineered, holds great promise as a novel ‘Precision Mining’ process for the rapid and selective Cu recovery from acidic wastewater, process effluents and leach liquors

Wild oat nutrient uptake and release from residue

Non-Peer Reviewe

Impact of in-crop and soil residual herbicides on effective nitrogen fixation in field pea (Pisum sativum L.) and chickpea (Cicer arietinum L.)

Non-Peer ReviewedA three-year project was initiated in 2004 to examine the effects of residual herbicides and registered “in-crop” herbicides, both soil and foliar applied, on N fixation and consequent yield of field peas and chickpeas. Inoculation strategies were examined to determine if inoculant formulation (i.e., peat powder versus granular inoculant) influences the degree to which herbicides can affect N fixation. This research is ongoing and thus all results are considered preliminary. Preliminary results in field pea, suggest that where herbicides had a negative effect on N fixation, the effects occurred at relatively early growth stages (i.e., soon after herbicide application) and were typically overcome at later growth stages. In addition, granular inoculants were associated with increased N fixation as compared to peat powder inoculants, and may have mitigated any negative herbicide effects. Chickpea incurred damage from the herbicides and all treatments had significantly less N fixation than the control. In general, results suggest that N fixation may be compromised if herbicides cause significant plant damage; however, improved weed control associated with herbicide application may counter the negative impact on early N fixation

Development and application of a bioassay for detection of sulfentrazone in soil

Non-Peer Reviewe

A confounding effect of ammonium toxicity on bioassay detection of thiencarbazone in soil

Non-Peer Reviewe

Determination of thiencarbazone in soil by the mustard root length bioassay

Non-Peer Reviewe

Effect of soil pH on sulfentrazone phytotoxicity

Non-Peer Reviewe