Simon A. Jackman
University of Oxford
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Simon A. Jackman.
Journal of Chemical Technology & Biotechnology | 2000
Giacomo Maini; Ajay K Sharman; Christopher J. Knowles; Garry Sunderland; Simon A. Jackman
The electrokinetic remediation of an historically contaminated soil is described. The soil was contaminated with a range of metals including lead, zinc, manganese, copper and arsenic, polycyclic aromatic hydrocarbons (PAHs) and benzene, toluene, ethylbenzene and xylene (BTEX). A small-scale experiment (973.2 g dry weight soil), utilising a planar electrode configuration, investigated the potential for moving metals and organics. After 23 days treatment at a current density of 3.72 A /m−2, 44% of calcium and 29% of manganese were removed from the soil at the cathode. Of the other contaminating metals, zinc and lead moved towards the cathode, but with no significant removal from the soil. Movement of PAHs was also observed, with a 94% reduction in concentration in the third of the soil closest to the anode after 23 days. A larger scale experiment (46.7 kg dry weight soil) utilised a hexagonal array of tubular anodes surrounding a central tubular cathode. Treatment for 112 days led to acidification of the soil to pH 2.59 closest to the anode in a direct line between the anode and cathode. Soil not directly in line between the electrodes was not acidified significantly. Movement of metal ions was observed, in line with the electrodes, with concentrations of lead and arsenic increasing to 162% and 171% of starting concentrations closest to the anode, respectively, and those of zinc, copper and manganese decreasing to 42%, 68% and 57%, respectively. At positions not directly in line with the electrodes, no significant metal movements were observed. Overall, there was no significant removal of contaminating metals from the soil. PAHs and BTEX compounds were moved by electroosmosis towards the cathode, with soil concentrations of PAHs reduced from 720 mgkg−1 to 4.7 mgkg−1 after 22 days. PAHS (28 mg) and benzene (9660 mg) were recovered in granular activated carbon (GAC) columns. © 2000 Society of Chemical Industry
Enzyme and Microbial Technology | 1999
Simon A. Jackman; Giacomo Maini; Ajay K Sharman; Christopher J. Knowles
Abstract The application of direct electric current to soil to remove metal ions is an emerging remediation technology. The combination of this approach with bioremediation requires that soil bacteria be viable and metabolically active under the applied currents (20 mA cm −2 ) and their imposed acidic conditions. In this study, sulfur-oxidizing bacteria (SOBs; a mixed culture and pure culture of Thiobacillus ferrooxidans ) growing on elemental sulfur, and the acidophilic heterotroph Acidiphilium SJH, growing on glucose, have been chosen as representative organisms. In liquid culture, low cell densities of T. ferrooxidans and Acidiphilium SJH were inactivated by the current; however, a high cell density of SOBs was able to recover activity when the current was switched off, and a high density of Acidiphilium SJH was able to grow despite the presence of current. In soil slurries (5, 10, and 30% w/v silt soil), indigenous SOBs were metabolically active in the presence of current; sulfate production was enhanced. There was also enhanced glucose consumption of Acidiphilium SJH in 10 and 30% slurries; however, no protective effect or increased metabolism occurred when T. ferrooxidans was introduced into soil slurries.
Chemosphere | 2010
Robert J. Barnes; Olga Riba; Murray N. Gardner; Andrew C. Singer; Simon A. Jackman; Ian P. Thompson
Iron (Fe) nanoparticles are increasingly being employed for the remediation of Chlorinated Aliphatic Hydrocarbon (CAH) contaminated sites. However, these particles have recently been reported to be cytotoxic to bacterial cells, and may therefore have a negative impact on exposed microbial communities. The overall objective of this study was to investigate the impact of Fe nanoparticles on the biodegradation of CAHs by an indigenous dechlorinating bacterial community. Also, to determine the most appropriate combination and/or application of bimetallic (Ni/Fe) nanoparticles and dechlorinating bacteria for the remediation of CAH contaminated sites. Addition of Fe nanoparticles to groundwater collected from a CAH contaminated site in Derby, UK, led to a decrease in the oxidation-reduction potential (ORP) and an increase in pH. The biological degradation rate of TCE was observed to progressively decrease in the presence of increasing Fe nanoparticle concentrations; which ranged from 0.01 to 0.1 gL(-1), and cease completely at concentrations of 0.3 gL(-1) or above. Concentrations greater than 0.3 gL(-1) led to a decline in viable bacterial counts and the inhibition of biological sulphate reduction. The most appropriate means of combining bimetallic (Ni/Fe) nanoparticles and indigenous dechlorinating bacteria was to employ a two step process: initially stimulating the biodegradation of TCE using acetate, followed by the addition of bimetallic nanoparticles to degrade the remaining cis-1,2-DCE and VC.
Chemosphere | 2010
Robert J. Barnes; Olga Riba; Murray N. Gardner; Thomas Bligh Scott; Simon A. Jackman; Ian P. Thompson
The use of nano-scale particles as a means of environmental remediation still provides a comparatively novel approach for the treatment of contaminated waters. The current study compares the reactivity of micro-scale Fe, nano-scale Fe and nano-scale Ni/Fe (nickel/iron) particles specifically for dechlorination of solutions containing 350 mg L(-1) of TCE (concentration measured at a contaminated site in Derbyshire, UK). The results indicated that employing 1 g L(-1) of reactive material for dechlorination in the monometallic form (both micro- and nano-scale) exhibited very little reduction capability compared with the bimetallic Ni/Fe nano-scale particles, containing 28.9% Ni (in molar), which achieved complete dechlorination of the TCE in solution within 576 h. Experiments were also performed to determine the optimum bimetallic composition of the Ni/Fe particles for TCE reduction. This revealed that 3.2% Ni was the optimum Ni/Fe molar ratio for both maximum dehalogenation performance and minimum release of Ni into solution. Using particles of the most effective bimetallic composition, experiments were carried out to determine the concentration required for optimal TCE reduction. Over the range of nano-scale particle concentrations tested (0.1-9 g L(-1)), reduction rates of TCE increased with greater TCE:nano-scale particle ratios. However, a concentration range of 1-3 g L(-1) was selected as the most appropriate for site remediation, since more concentrated solutions demonstrated only small increases in rates of reaction. Finally, in order to test the long term performance and reactivity of the 3.2% Ni/Fe bimetallic nano-scale particles, weekly spikes of 350 mg L(-1) TCE were injected into a 3 g L(-1) nano-scale particle batch reactor. Results showed that the bimetallic nano-scale particles had the ability to reduce 1750 mg L(-1) TCE and remained active for at least 13 weeks.
Environmental Health Perspectives | 2008
Andrew C. Singer; Bruce M. Howard; Andrew C. Johnson; Chris Knowles; Simon A. Jackman; Cesare Accinelli; Anna Barra Caracciolo; Ian Bernard; Stephen Bird; Tatiana Boucard; Alistair B.A. Boxall; Jayne V. Brian; Elise Cartmell; Chris Chubb; John Churchley; Sandra Costigan; Mark Crane; Michael J. Dempsey; Bob Dorrington; Brian Ellor; Jerker Fick; John Holmes; Tom Hutchinson; Franz Karcher; Samuel L. Kelleher; Peter Marsden; Gerald Noone; Miles A. Nunn; John Oxford; Tony Rachwal
On 3 October 2007, 40 participants with diverse expertise attended the workshop Tamiflu and the Environment: Implications of Use under Pandemic Conditions to assess the potential human health impact and environmental hazards associated with use of Tamiflu during an influenza pandemic. Based on the identification and risk-ranking of knowledge gaps, the consensus was that oseltamivir ethylester-phosphate (OE-P) and oseltamivir carboxylate (OC) were unlikely to pose an ecotoxicologic hazard to freshwater organisms. OC in river water might hasten the generation of OC-resistance in wildfowl, but this possibility seems less likely than the potential disruption that could be posed by OC and other pharmaceuticals to the operation of sewage treatment plants. The work-group members agreed on the following research priorities: a) available data on the ecotoxicology of OE-P and OC should be published; b) risk should be assessed for OC-contaminated river water generating OC-resistant viruses in wildfowl; c) sewage treatment plant functioning due to microbial inhibition by neuraminidase inhibitors and other antimicrobials used during a pandemic should be investigated; and d) realistic worst-case exposure scenarios should be developed. Additional modeling would be useful to identify localized areas within river catchments that might be prone to high pharmaceutical concentrations in sewage treatment plant effluent. Ongoing seasonal use of Tamiflu in Japan offers opportunities for researchers to assess how much OC enters and persists in the aquatic environment.
Tetrahedron | 2004
Hong Li; Roberta Mustacchi; Christopher J. Knowles; Wolfgang Skibar; Garry Sunderland; Ian Dalrymple; Simon A. Jackman
Environmental Science & Technology | 2000
Giacomo Maini; Ajay K Sharman; Garry Sunderland; Christopher J. Knowles; Simon A. Jackman
Biotechnology and Bioengineering | 2001
Simon A. Jackman; Giacomo Maini; Ajay K Sharman; Garry Sunderland; Christopher J. Knowles
Biotechnology and Bioengineering | 2005
Roberta Mustacchi; Christopher J. Knowles; Hong Li; Ian Dalrymple; Garry Sunderland; Wolfgang Skibar; Simon A. Jackman
Archive | 2003
Christopher J. Knowles; Simon A. Jackman; Li Hong; Roberta Mustacchi; John Garry Sunderland