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Simon A Parsons

Publications and source records attributed to Simon A Parsons.

12 recordsLinked to original sources

Prioritization of pesticide environmental transformation products in drinking water supplies.

Receiving waters within catchments may be exposed to many different transformation products following the application of pesticides. As environmental waters are abstracted for drinking water treatment these compounds may pose a risk to human health. This paper describes a prioritization approach for identifying the most important transformation products in drinking water sources. The approach can be applied to different geographical areas that have suitable pesticide usage data. The risk based approach incorporates data on pesticide usage and toxicity as well as transformation product formation, mobility, and persistence. The application of the approach is illustrated for two geographical areas that have good quality pesticide usage data: Great Britain and California. The transformation products with the highest risk index and a complete experimentally derived data set for Great Britain were 3,5,6-trichloro-2-pyridinol, thifensulfuron acid, and kresoxim-methyl acid and for California were carbendazim, aldicarb sulfoxide, and RP30228.

California↗

Agglomeration of struvite crystals.

Struvite crystallisation is widely studied as a way to remove phosphorus from wastewater effluents and simultaneously generates a valuable product for the fertiliser industry. However, to date, some crystallisation processes experimented at either pilot/or full scale face problems linked to the formation of fines. This paper presents results on the investigation of struvite agglomerative properties and the possible application of coagulants and/or flocculants to remove fines. Coagulants investigated were hydrolysing metals salts (Al(3+) and Fe(3+)), calcium compounds and a cationic polymer, polydiallyldimethylammoniumchloride (polyDADMAC). The effects of a natural flocculant (alginate) have also been tested. Results demonstrated that destabilisation of struvite particles by chemical addition was feasible and identified polyDADMAC as a good option for the agglomeration of struvite particles. However, optimisation of its dosage under typical pH conditions for struvite formation showed floc formation to be very pH sensitive.

Alginates↗

The impact of zeta potential on the physical properties of ferric--NOM flocs.

The physical properties of natural organic matter (NOM) flocs, such as size, growth rate, and strength, were investigated using a laser diffraction particle sizing device. Conditions were set such that varying carbon coagulant ratio and zeta potential could both be investigated. Results demonstrated a link between zeta potential and coagulation and flocculation performance, with the production of strong flocs and low residual concentrations when the zeta potential was minimized. The overall strength of the connection points within the floc were determined by a combination of steric interactions, polymer bridging, van der Waals forces, and electrostatic forces. Hence, both dose ratio and zeta potential are important in understanding floc properties. Floc growth was dominated by dose ratio, whereas the response to elevated shear was strongly related to zeta potential. The steady-state floc size was a combination of both factors. This allowed the continued development of a qualitative model in order to engineer optimal floc properties when coagulating NOM.

Ferric Compounds↗

An investigation into reservoir NOM reduction by UV photolysis and advanced oxidation processes.

A comparison of four treatment technologies for reduction of natural organic matter (NOM) in a reservoir water was made. The work presented here is a laboratory based evaluation of NOM treatment by UV-C photolysis, UV/H(2)O(2), Fenton's reagent (FR) and photo-Fenton's reagent (PFR). The work investigated ways of reducing the organic load on water treatment works (WTWs) with a view to treating 'in-reservoir' or 'in-pipe' before the water reaches the WTW. The efficiency of each process in terms of NOM removal was determined by measuring UV absorbance at 254 nm (UV(254)) and dissolved organic carbon (DOC). In terms of DOC reduction PFR was the most effective (88% removal after 1 min) however there were interferences when measuring UV(254) which was reduced to a lesser extent (31% after 1 min). In the literature, pH 3 is reported to be the optimal pH for oxidation with FR but here the reduction of UV(254) and DOC was found to be insensitive to pH in the range 3-7. The treatment that was identified as the most effective in terms of NOM reduction and cost effectiveness was PFR.

Carbon↗

Floc structural characteristics using conventional coagulation for a high doc, low alkalinity surface water source.

Removal of natural organic matter (NOM) is well established using metal salt coagulants. In addition, flocculant aids are also commonly used to improve solid removal. The objectives of this paper is to describe the impacts of both NOM and polymer on floc structure. The study offers a comparison of floc physical characteristics for coagulant precipitate flocs, organic-coagulant flocs and organic-coagulant-polymer flocs for optimum coagulant and polymer doses. A ferric sulphate-based coagulant was used as the primary coagulant and the polymer selected was a high molecular weight (MW) cationic polydiallyldimethylammonium chloride (polyDADMAC). Floc size, breakage, re-growth and settling characteristics were measured. Precipitate flocs were larger than organic flocs and had better settling characteristics when compared to NOM-coagulant flocs. When polymer was added, floc size and compaction was seen to further reduce. An explanation was offered in terms of the mode of flocculation involved. Floc breakage behaviour showed that polymer reduced the rate of floc degradation but did not greatly improve floc re-growth potential after breakage, which was generally poor for all of the suspensions.

Alkalies↗

How the natural organic matter to coagulant ratio impacts on floc structural properties.

Periods of elevated natural organic matter (NOM) loadings at water treatment works (WTW) can lead to operational problems as a result of deterioration in floc structural quality. This study used a range of diagnostic tools to evaluate floc structure with increasing organic fraction in the floc. It was observed that when the organic fraction in the floc went significantly over a mass ratio of 1 mg of DOC to 1 mg of Fe (coagulant), the floc size, settling velocity, fractal dimension, and strength were seen to decrease even when the NOM removed during coagulation remained high. A model was proposed to explain these changes that was dependent upon the adsorption of NOM on primary particle surfaces. The operational significance of these results suggests that for the coagulant under investigation the correct coagulant dose must be applied to give good floc structure.

Ferric Compounds↗

The impact of seasonal variations in DOC arising from a moorland peat catchment on coagulation with iron and aluminium salts.

Natural organic matter (NOM) is one of the main sources of environmental pollution to drinking water supplies in much of the UK and the US. Whilst traditional treatment with trivalent coagulants has proven a successful strategy in the past, operational problems are now being reported during periods of elevated organic levels in the water. Characterisation of the pollutants in terms of polarity, molecular weight and charge, provides a method to understand the impact of the observed temporal and spatial variations in terms of a mechanistic parameter relevant to the treatment processes. Results from this study demonstrate that it is not simply the increased organic concentration, but also the change in NOM composition and character, which influences the impact on the treatment processes. Consequently, monitoring of these parameters provides an insight into how to manage the impact caused by environmental changes to the catchments.

Aluminum↗

Seasonal variations in natural organic matter and its impact on coagulation in water treatment.

In the past decade, a number of UK and US water utilities have been experiencing operational difficulties connected with the increased dissolved organic carbon (DOC) levels during the autumn and winter periods. This has been observed as an increase in the production of disinfection-by-products (DBP), and a greater coagulant demand. Resin adsorption techniques were used to fractionate raw water and investigate the variation in surface charge and coagulant-humic interactions over a 36-month period. A change in the natural organic matter (NOM) composition throughout the year was observed, with the fulvic acid fraction (FAF) increasing from 36% in September to 61% in November. However, a reduction in treatment performance is not simply due to an increase in DOC concentrations (from 4.3 to 14.5 mg L-1), but also a change in the charge density of the NOM. It was found that hydrophilic NOM fractions possess negligible charge density (<0.06 meq g-1DOC), and it is the hydrophobic NOM fractions, FAF in particular, that exert the greater dominance on coagulation control. The hydrophilic NOM fractions are less amenable to removal through conventional coagulation with metal salts, and are therefore likely to indicate the DOC residual remaining after treatment. Understanding the seasonal changes in NOM composition and character and their reactivity with coagulants should lead to a better optimisation of the coagulation process and a more consistent water quality.

Journal Article↗

Breakage, regrowth, and fractal nature of natural organic matter flocs.

The growth, breakage, regrowth, and fractal nature of flocs was investigated by use of a laser diffraction particle sizing device. A range of coagulants were investigated for the coagulation of natural organic matter (NOM) and compared to other coagulated systems. The results showed NOM floc structural characteristics varied in steady-state size depending upon which coagulant was used. When compared to other systems, the order of floc size was Fe precipitate > Fe-NOM > latex (in NaCl solution). Floc regrowth after exposure to high shear was limited for all of the flocs under investigation other than for latex in an inert electrolyte. This highlighted differences in the internal bonding structure of flocs, with the results suggesting that physical bonds have a capacity to re-form after breakage. Fractal dimension analysis by small-angle laser light scattering (SALLS) had limited applicability to large flocs that dominated all of the systems under investigation, but the degree of compaction increased as flocs were broken in high shear. This provided a possible mechanistic reason for the irreversible breakage seen.

Alum Compounds↗

Removal of NOM from drinking water: Fenton's and photo-Fenton's processes.

The control of disinfection by-products during water treatment is primarily undertaken by reducing the levels of precursor species prior to chlorination. As many waters contain natural organic matter at levels of up to 15 mgl(-1) there is a need for a range of control methods to support conventional coagulation. Two such processes are the Fenton and photo-Fenton's processes and in this paper they are assessed for their potential to remove NOM from organic rich waters. The performance of both processes is shown to be depentent on pH, Fe: H2O2 ratio as well as Fe2+ dose. Under optimum conditions both processes achieved greater than 90% removal of DOC and UV254 absorbance. This removal lead to the trihalomethane formation potential of the water being reduced from 140 to below 10 microgl(-1), well below UK and US standards.

Chromatography, Gel↗

A model for predicting dissolved organic carbon distribution in a reservoir water using fluorescence spectroscopy.

A number of water treatment works (WTW) in the north of England (UK) have experienced problems in reducing the dissolved organic carbon (DOC) present in the water to a sufficiently low level. The problems are experienced in autumn/winter when the colour increases and the coagulant dose at the WTW needs to be increased in order to achieve sufficient colour removal. However, the DOC content of the water varies little throughout the year. To investigate this further, the water was fractionated using resin adsorption techniques into its hydrophobic (fulvic and humic acid fractions) and hydrophilic (acid and non-acid fractions) components. The fractionation process yields useful information on the changing concentration of each fraction but is time consuming and labour intensive. Here, a method of rapidly determining fraction concentration was developed using fluorescence spectroscopy. The model created used synchronous spectra of fractionated material compared against bulk water spectra and predicted the fraction concentrations to within 10% for a specific water. The model was unable to predict fraction concentrations for waters from a different watershed.

Carbon↗

Struvite formation, control and recovery.

Recent legislation on the removal of nutrients from wastewater has led to a number of operation problems with struvite scaling. Struvite is MgNH4PO4 x 6H2O and this paper reviews the formation, control and recovery of struvite from primarily municipal wastewater and other waste streams. Treatment options for control and technologies for recovery are discussed.

Chemical Precipitation↗