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The Remediation of Chemical Groundwater Contamination at Harwell

The Remediation of Chemical Groundwater Contamination at Harwell

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<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong><strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong><strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>Report to the <strong>Harwell</strong> Chilton CampusLocal Stakeholder Group:March 2009<strong>Harwell</strong> <strong>Groundw<strong>at</strong>er</strong> Containment Plant


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>LSG <strong>Groundw<strong>at</strong>er</strong> Report ii March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>THE REMEDIATION OF CHEMICAL GROUNDWATERCONTAMINATION AT HARWELLIssue D<strong>at</strong>e Author Checked by Approved byA March 09 Name Jon Blackmore Paul Atyeo Ken HeiderRole Project Manager Senior Project Closure DirectorManagerSign<strong>at</strong>ureD<strong>at</strong>eLSG <strong>Groundw<strong>at</strong>er</strong> Report iii March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>LSG <strong>Groundw<strong>at</strong>er</strong> Report iv March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>EXECUTIVE SUMMARY<strong>Chemical</strong> contamin<strong>at</strong>ion <strong>of</strong> groundw<strong>at</strong>er <strong>at</strong> <strong>Harwell</strong> was first identified in the l<strong>at</strong>e1980s. This contamin<strong>at</strong>ion, principally by chlorin<strong>at</strong>ed organic chemicals, wassubsequently linked to the disposal <strong>of</strong> waste chemicals in unlined chalk pits <strong>at</strong><strong>Harwell</strong>. <strong>The</strong>se waste disposal pits were loc<strong>at</strong>ed <strong>at</strong> the Southern Storage Area(SSA), formerly used by the RAF for munitions storage, and the Western StorageArea (WSA). RSRL has subsequently undertaken a major programme <strong>of</strong> work toinvestig<strong>at</strong>e and deal with the contamin<strong>at</strong>ion. This report presents developments inrel<strong>at</strong>ion to the groundw<strong>at</strong>er programme <strong>at</strong> <strong>Harwell</strong> during 2008.<strong>The</strong> groundw<strong>at</strong>er containment plant (HGCP) continues to maintain effective hydrauliccontainment <strong>at</strong> the WSA. This was confirmed by the w<strong>at</strong>er level measurements madeduring 2008.HGCP has realised improvements over the original plant in terms <strong>of</strong> health andsafety, energy consumption, waste gener<strong>at</strong>ion and ease and flexibility <strong>of</strong> oper<strong>at</strong>ion.Energy consumption is 30% <strong>of</strong> th<strong>at</strong> used by the old groundw<strong>at</strong>er plant.<strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> the uns<strong>at</strong>ur<strong>at</strong>ed zone <strong>at</strong> the WSA has continued during 2008,removing a further 795 kg <strong>of</strong> contaminants. <strong>The</strong> total removed by the uns<strong>at</strong>ur<strong>at</strong>edzone project is now nearly 1.8 tonnes. Up to three further phases <strong>of</strong> uns<strong>at</strong>ur<strong>at</strong>edzone remedi<strong>at</strong>ion are planned.<strong>The</strong> total mass <strong>of</strong> contamin<strong>at</strong>ion removed by the different components <strong>of</strong> theremedi<strong>at</strong>ion programme is now estim<strong>at</strong>ed to be approxim<strong>at</strong>ely 11 tonnes.LSG <strong>Groundw<strong>at</strong>er</strong> Report v March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>GLOSSARYAODAquiferBoreholeChlorin<strong>at</strong>edsolventsGAC<strong>Groundw<strong>at</strong>er</strong>LevelHGCP<strong>Remedi<strong>at</strong>ion</strong>SSASVETEVEUns<strong>at</strong>ur<strong>at</strong>edzoneVacuumextractionVOCsW<strong>at</strong>er TableWSAZone <strong>of</strong>w<strong>at</strong>er tablefluctu<strong>at</strong>ionAbove Ordnance D<strong>at</strong>um. <strong>The</strong> height <strong>of</strong> a point (eg the w<strong>at</strong>er table or groundlevel) above mean sea level (the Newlyn d<strong>at</strong>um, since 1921), usually expressedin metres (eg 120 m AOD).An aquifer is a permeable rock th<strong>at</strong> stores and allows groundw<strong>at</strong>er flow readilythrough it.A deep, narrow vertical shaft used for the extraction or monitoring <strong>of</strong> groundw<strong>at</strong>eror soil vapour. Typically, boreholes drilled <strong>at</strong> <strong>Harwell</strong> in rel<strong>at</strong>ion to the chemicalgroundw<strong>at</strong>er contamin<strong>at</strong>ion programme are between 50 and 200 mm in diameterand up to 55 metres deep.Liquids used to remove grease from metal components in engineering workshopsand also as labor<strong>at</strong>ory reagents. <strong>The</strong>se were disposed <strong>of</strong> in large quantities to thewaste pits <strong>at</strong> the SSA and WSA. <strong>The</strong> principal groundw<strong>at</strong>er contaminants are allchlorin<strong>at</strong>ed solvents:• carbon tetrachloride;• chlor<strong>of</strong>orm;• 1,1,1-trichloroethane;• trichloroethene; and• tetrachloroethene.Chlorin<strong>at</strong>ed solvents form part <strong>of</strong> a larger grouping <strong>of</strong> chemicals called VOCs(see below).Granular Activ<strong>at</strong>ed Carbon. A product <strong>of</strong>ten derived from coal or coconut husks,which readily adsorbs organic chemicals. Widely used in many industries for thetre<strong>at</strong>ment <strong>of</strong> contamin<strong>at</strong>ed liquids and gases.See W<strong>at</strong>er Table.<strong>Harwell</strong> <strong>Groundw<strong>at</strong>er</strong> Containment Plant – the replacement w<strong>at</strong>er tre<strong>at</strong>ment plant<strong>at</strong> the WSA, which became fully oper<strong>at</strong>ional in June 2007.In the context <strong>of</strong> pollution, used to describe works carried out to reduce theimpact <strong>of</strong> the pollution.Southern Storage Area. <strong>The</strong> former RAF bomb dump, used for wastemanagement and disposal oper<strong>at</strong>ions by UKAEA from the 1940s to the 1970s.Soil Vapour Extraction. A technique used for removing VOC contamin<strong>at</strong>ion fromsoils and rocks, usually above the w<strong>at</strong>er table.<strong>The</strong>rmally enhanced vacuum extraction. Collective term for a group <strong>of</strong> techniqueswhich use he<strong>at</strong> energy to improve the r<strong>at</strong>e <strong>of</strong> contaminant removal using SVE. Inthe case <strong>of</strong> the WSA project, conductive he<strong>at</strong>ing elements are used to he<strong>at</strong> thechalk above the w<strong>at</strong>er table.<strong>The</strong> part <strong>of</strong> the aquifer above the w<strong>at</strong>er table.See SVE.Vol<strong>at</strong>ile Organic Compounds. A broad grouping for a range <strong>of</strong> different organiccompounds characterised by their readiness to evapor<strong>at</strong>e under normalconditions. Many <strong>of</strong> the chlorin<strong>at</strong>ed solvents fall within this c<strong>at</strong>egory.Th<strong>at</strong> level bene<strong>at</strong>h the land <strong>at</strong> which the pores <strong>of</strong> rock or soil become completelyfull <strong>of</strong> groundw<strong>at</strong>er. Also referred to as the groundw<strong>at</strong>er level.Western Storage Area. Licensed landfill, used for the disposal <strong>of</strong> chemical wastesfrom the 1970s to 1980s.<strong>The</strong> part <strong>of</strong> the chalk th<strong>at</strong> is between the lowest and highest observed w<strong>at</strong>er tablelevels. At <strong>Harwell</strong>, the Chalk w<strong>at</strong>er table fluctu<strong>at</strong>es by up to 18 metres, from thelowest to highest levels. Depending on the elev<strong>at</strong>ion <strong>of</strong> the w<strong>at</strong>er table, this part<strong>of</strong> the aquifer may be available for SVE or TEVE.LSG <strong>Groundw<strong>at</strong>er</strong> Report vi March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>CONTENTSEXECUTIVE SUMMARY............................................................................................ 5Glossary ..................................................................................................................... 61 Introduction.......................................................................................................... 12 <strong>Groundw<strong>at</strong>er</strong> Levels ............................................................................................ 33 <strong>Groundw<strong>at</strong>er</strong> Containment, Western Storage Area ............................................. 64 Uns<strong>at</strong>ur<strong>at</strong>ed Zone <strong>Remedi<strong>at</strong>ion</strong>, WSA............................................................... 105 <strong>Groundw<strong>at</strong>er</strong> Monitoring.................................................................................... 126 Summary ........................................................................................................... 15FiguresFigure 1 Loc<strong>at</strong>ion <strong>of</strong> the Western and Southern Storage Areas <strong>at</strong> <strong>Harwell</strong> ................ 2Figure 2 Geological map <strong>of</strong> the <strong>Harwell</strong> Area ............................................................. 2Figure 3 <strong>Groundw<strong>at</strong>er</strong> levels (“w<strong>at</strong>er table”) in the Chalk <strong>at</strong> <strong>Harwell</strong> (Borehole HWS9),1991 to 2009 ................................................................................................ 4Figure 4 Annual vari<strong>at</strong>ion in groundw<strong>at</strong>er levels in Borehole HWS9 during 2007 and2008 in comparison to d<strong>at</strong>a since 1991........................................................ 4Figure 5 Map <strong>of</strong> <strong>Harwell</strong> site showing groundw<strong>at</strong>er levels and groundw<strong>at</strong>er flowdirections in the Chalk aquifer, April & October 2008................................... 5Figure 6 Schem<strong>at</strong>ic represent<strong>at</strong>ion <strong>of</strong> the hydraulic containment <strong>of</strong> groundw<strong>at</strong>ercontamin<strong>at</strong>ion <strong>at</strong> the Western Storage Area................................................. 6Figure 7 Annual quantities <strong>of</strong> groundw<strong>at</strong>er tre<strong>at</strong>ed and contaminant mass removedby the Western <strong>Groundw<strong>at</strong>er</strong> Plant .............................................................. 9Figure 8 Total contaminant concentr<strong>at</strong>ions in the w<strong>at</strong>er pumped into the Western<strong>Groundw<strong>at</strong>er</strong> Plant ....................................................................................... 9Figure 9 Illustr<strong>at</strong>ion <strong>of</strong> remedi<strong>at</strong>ion techniques for the uns<strong>at</strong>ur<strong>at</strong>ed zone and zone <strong>of</strong>w<strong>at</strong>er table fluctu<strong>at</strong>ion <strong>at</strong> the Western Storage Area .................................. 11Figure 10 Install<strong>at</strong>ion <strong>of</strong> conductive he<strong>at</strong>ing elements in boreholes for the TEVEsystem........................................................................................................ 11Figure 11 Total contaminant concentr<strong>at</strong>ions (CHCs - chlorin<strong>at</strong>ed hydrocarbons),April and October 2008 .............................................................................. 13Figure 12 Vari<strong>at</strong>ion in total contaminant concentr<strong>at</strong>ion with time in boreholeHWS1 (150 metres north <strong>of</strong> the WSA) ....................................................... 14Figure 13 Vari<strong>at</strong>ion in total contaminant concentr<strong>at</strong>ion with time in boreholeHWS10 (200 metres southeast <strong>of</strong> the WSA) .............................................. 14Figure 14 Summary <strong>of</strong> contaminant mass removal by year ................................ 15LSG <strong>Groundw<strong>at</strong>er</strong> Report vii March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>LSG <strong>Groundw<strong>at</strong>er</strong> Report viii March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>1 INTRODUCTION<strong>Contamin<strong>at</strong>ion</strong> <strong>of</strong> the groundw<strong>at</strong>er bene<strong>at</strong>h the <strong>Harwell</strong> site was first detected in l<strong>at</strong>e 1989.Investig<strong>at</strong>ions revealed the presence <strong>of</strong> chlorin<strong>at</strong>ed organic solvents in the groundw<strong>at</strong>er,which were linked to disposal <strong>of</strong> wastes in a number <strong>of</strong> shallow, unlined pits <strong>at</strong> theSouthern (SSA) and Western (WSA) Storage Areas (Figure 1). Both disposal sites areloc<strong>at</strong>ed on the Chalk aquifer, as indic<strong>at</strong>ed by the areas underlain by green shading onFigure 2.<strong>The</strong> Southern Storage Area (SSA) was the older <strong>of</strong> the two disposal sites. It was loc<strong>at</strong>edbetween <strong>Harwell</strong> site and Chilton, and was first used for munitions storage when <strong>Harwell</strong>was a Second World War RAF airfield. <strong>The</strong> SSA was used immedi<strong>at</strong>ely after the SecondWorld War for the early waste management oper<strong>at</strong>ions <strong>of</strong> the former Atomic EnergyResearch Establishment <strong>at</strong> <strong>Harwell</strong>. <strong>Chemical</strong> wastes were disposed <strong>of</strong> on the site until1970, when oper<strong>at</strong>ions were transferred to a new site, loc<strong>at</strong>ed on the western boundary <strong>of</strong>the main <strong>Harwell</strong> site.This second site was the Western Storage Area (WSA), which included a compound with25 unlined pits. <strong>The</strong> site was originally licensed under the Control <strong>of</strong> Pollution Act 1974 byOxfordshire County Council. <strong>The</strong> pits on the site were used for the disposal <strong>of</strong> variouschemical wastes, including chlorin<strong>at</strong>ed solvents and other organic chemicals. <strong>The</strong>chlorin<strong>at</strong>ed solvent disposals occurred over the period from 1970 to 1977; after this time,wastes were sent <strong>of</strong>f-site for inciner<strong>at</strong>ion. <strong>The</strong> site is now licensed as a closed landfill bythe Environment Agency (EA).Following the discovery <strong>of</strong> the groundw<strong>at</strong>er contamin<strong>at</strong>ion, a programme <strong>of</strong> work wasimplemented to deline<strong>at</strong>e, contain and then remedi<strong>at</strong>e the groundw<strong>at</strong>er contamin<strong>at</strong>ion andits sources. An extensive programme <strong>of</strong> groundw<strong>at</strong>er monitoring is also undertaken, inconjunction with the EA.This report, covering the period January to December 2007, provides an annual upd<strong>at</strong>e onthe st<strong>at</strong>us <strong>of</strong> the groundw<strong>at</strong>er programme to the March 2009 meeting <strong>of</strong> the <strong>Harwell</strong>-Chilton Campus Local Stakeholder Group (LSG).LSG <strong>Groundw<strong>at</strong>er</strong> Report 1 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>© Crown Copyright 2005. All rights reserved. OrdnanceSurvey Licence Number 10047376.Figure 1Loc<strong>at</strong>ion <strong>of</strong> the Western and Southern Storage Areas <strong>at</strong> <strong>Harwell</strong>Figure 2Geological map <strong>of</strong> the <strong>Harwell</strong> AreaLSG <strong>Groundw<strong>at</strong>er</strong> Report 2 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>2 GROUNDWATER LEVELS<strong>The</strong> vari<strong>at</strong>ion in groundw<strong>at</strong>er levels (the “w<strong>at</strong>er table”) with time in the Chalk aquifer under<strong>Harwell</strong> site is shown in Figure 3. <strong>The</strong>se d<strong>at</strong>a rel<strong>at</strong>e to borehole HWS9 (Figure 1), whichhas been monitored weekly since 1991. <strong>Groundw<strong>at</strong>er</strong> levels are relevant to themanagement <strong>of</strong> groundw<strong>at</strong>er contamin<strong>at</strong>ion for a number <strong>of</strong> reasons:1. Historically, as groundw<strong>at</strong>er levels have risen (usually in the l<strong>at</strong>e autumn and winter)contamin<strong>at</strong>ion has been washed out from the Chalk bene<strong>at</strong>h the waste pits <strong>at</strong> theWSA, resulting in higher contaminant concentr<strong>at</strong>ions in the groundw<strong>at</strong>er captured bythe containment plant.2. Away from the WSA, the rel<strong>at</strong>ionship between groundw<strong>at</strong>er levels and contaminantconcentr<strong>at</strong>ions is the opposite. At times <strong>of</strong> high groundw<strong>at</strong>er levels, concentr<strong>at</strong>ions arelowest, because <strong>of</strong> dilution <strong>of</strong> the contaminants by rainfall entering the aquifer. Whengroundw<strong>at</strong>er levels are low, contaminant concentr<strong>at</strong>ions rise.3. In the Chalk aquifer bene<strong>at</strong>h the northern part <strong>of</strong> the <strong>Harwell</strong> site, the direction <strong>of</strong>groundw<strong>at</strong>er flow changes depending on the groundw<strong>at</strong>er levels. At times <strong>of</strong> highgroundw<strong>at</strong>er levels, w<strong>at</strong>er flows from the springs <strong>at</strong> the top <strong>of</strong> the Lydebank Brook,resulting in groundw<strong>at</strong>er flows to the north from much <strong>of</strong> the site. As the groundw<strong>at</strong>erlevels fall flow from the springs stops and the dominant groundw<strong>at</strong>er flow directionchanges to the east and southeast. <strong>Groundw<strong>at</strong>er</strong> flows bene<strong>at</strong>h the southern part <strong>of</strong>the <strong>Harwell</strong> site do not show the same seasonal change in direction.<strong>The</strong> peak groundw<strong>at</strong>er level recorded in borehole HWS9 during 2008 was 110.8 m AOD,recorded on 25 March (Figure 3). <strong>Groundw<strong>at</strong>er</strong> levels then dropped until l<strong>at</strong>e May/EarlyJune, when groundw<strong>at</strong>er levels rose in response to heavy rainfall. Met Office d<strong>at</strong>a forOxford show th<strong>at</strong> the rainfall total for May and June 2008 was 60% above average 1 . Thiswas the second successive year in which summer recharge <strong>of</strong> groundw<strong>at</strong>er had occurred,something not seen since collection <strong>of</strong> groundw<strong>at</strong>er level d<strong>at</strong>a began <strong>at</strong> <strong>Harwell</strong> in 1990.Figure 4 shows groundw<strong>at</strong>er level d<strong>at</strong>a for borehole HWS9, re-plotted to allow comparison<strong>of</strong> d<strong>at</strong>a for each year. During the summer, groundw<strong>at</strong>er recharge usually does not occurbecause rainfall either evapor<strong>at</strong>es from the surface or is utilised by plants. However,Figure 4 shows th<strong>at</strong> groundw<strong>at</strong>er levels increased by 3.2 metres in response to heavyrainfall in July 2007 and by 1.3 metres in June 2008.From July 2008 onwards, groundw<strong>at</strong>er levels fell until early November, when groundw<strong>at</strong>erbegan to increase.<strong>The</strong> maps in Figure 5 show groundw<strong>at</strong>er levels in the Chalk in April and October 2008.<strong>The</strong> solid lines are contours <strong>of</strong> equal groundw<strong>at</strong>er level. <strong>The</strong> groundw<strong>at</strong>er flow direction isapproxim<strong>at</strong>ed by the arrows. <strong>The</strong>se plots coincide with the major six-monthly groundw<strong>at</strong>ersampling events undertaken by RSRL on site. April and October were selected as themain sampling events because they generally coincide with the highest and lowestgroundw<strong>at</strong>er levels respectively.<strong>The</strong> p<strong>at</strong>terns <strong>of</strong> groundw<strong>at</strong>er flow seen in 2008 (Figure 5) were similar to those seen in2007. <strong>The</strong> groundw<strong>at</strong>er level d<strong>at</strong>a show th<strong>at</strong> the groundw<strong>at</strong>er plant <strong>at</strong> the WSA maintainedeffective containment during 2008, continuing to prevent contamin<strong>at</strong>ed groundw<strong>at</strong>ermoving away from the WSA.1Based on d<strong>at</strong>a for the period 1971-2000LSG <strong>Groundw<strong>at</strong>er</strong> Report 3 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>120Ground level: approx. 120 mAOD115groundw<strong>at</strong>er level (metres AOD)110105100Total w<strong>at</strong>er table range approx. 18 metresW<strong>at</strong>er Table (Chalk Aquifer)95Jan-91Jan-92Jan-93Jan-94Jan-95Jan-96Jan-97Jan-98Jan-99Jan-00Jan-01Jan-02Jan-03Jan-04Jan-05Jan-06Jan-07Jan-08Jan-09Jan-10Figure 3<strong>Groundw<strong>at</strong>er</strong> levels (“w<strong>at</strong>er table”) in the Chalk <strong>at</strong> <strong>Harwell</strong> (BoreholeHWS9), 1991 to 2009120115<strong>Groundw<strong>at</strong>er</strong> levelincrease due to heavyrain, June 200820072008<strong>Groundw<strong>at</strong>er</strong> Level (m AOD)11010510095Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov DecFigure 4 Annual vari<strong>at</strong>ion in groundw<strong>at</strong>er levels in Borehole HWS9 during 2007and 2008 in comparison to d<strong>at</strong>a since 1991LSG <strong>Groundw<strong>at</strong>er</strong> Report 4 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>April 2008October 2008Figure 5Map <strong>of</strong> <strong>Harwell</strong> site showing groundw<strong>at</strong>er levels and groundw<strong>at</strong>er flowdirections in the Chalk aquifer, April & October 2008LSG <strong>Groundw<strong>at</strong>er</strong> Report 5 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>3.2 <strong>Groundw<strong>at</strong>er</strong> Plant Oper<strong>at</strong>ions 2008<strong>The</strong> groundw<strong>at</strong>er containment plant <strong>at</strong> the SSA was decommissioned in April 2002, withthe agreement <strong>of</strong> the EA. This followed the successful completion <strong>of</strong> the SSA landremedi<strong>at</strong>ion project.<strong>The</strong> original hydraulic containment plant <strong>at</strong> the WSA became fully oper<strong>at</strong>ional in 1994. <strong>The</strong>need for a replacement plant was identified several years ago because the original planthad reached the end <strong>of</strong> its design life, and predictions, based on extrapol<strong>at</strong>ion <strong>of</strong> themonitoring d<strong>at</strong>a for the original plant, indic<strong>at</strong>ed th<strong>at</strong> a containment plant could be neededuntil around 2025.<strong>The</strong> replacement plant, referred to as <strong>Harwell</strong> <strong>Groundw<strong>at</strong>er</strong> Containment Plant (HGCP),has been oper<strong>at</strong>ing very successfully since June 2007.HGCP uses granular activ<strong>at</strong>ed carbon (GAC) to remove the contaminants from thegroundw<strong>at</strong>er. GAC is used in domestic w<strong>at</strong>er filters, as well as many other applic<strong>at</strong>ions. Itis very effective <strong>at</strong> removing organic chemicals from w<strong>at</strong>er, and is robust and costeffective.<strong>The</strong> original groundw<strong>at</strong>er plant <strong>at</strong> the WSA used GAC to effect w<strong>at</strong>er tre<strong>at</strong>ment, but inconjunction with a process called air stripping. However, contaminant concentr<strong>at</strong>ions in thegroundw<strong>at</strong>er <strong>at</strong> the WSA have been successfully reduced to a level where liquid phaseGAC tre<strong>at</strong>ment alone is viable. This has simplified the design, oper<strong>at</strong>ion and regul<strong>at</strong>ion <strong>of</strong>HGCP, resulting in significant cost and environmental benefits. As an example, the airstripping system on the original plant required the oper<strong>at</strong>ion <strong>of</strong> a 27 kW he<strong>at</strong>er, and this isnot needed in HGCP.<strong>The</strong> liquid phase GAC filters themselves are an improvement over those used on theoriginal plant, which were fixed vessels. Removal <strong>of</strong> the spent GAC filter medium fromthese filters required personnel to enter the vessels. Although these oper<strong>at</strong>ions werealways managed safely, the opportunity to elimin<strong>at</strong>e industrial hazards such as confinedspace working and working <strong>at</strong> height was taken with HGCP.When the GAC used on HGCP requires replacement, the entire filter unit is transported ona special lorry to a regener<strong>at</strong>ion plant. Here the GAC is removed without the need forpersonnel to enter the vessel. <strong>The</strong> GAC is then tre<strong>at</strong>ed to remove and destroy thecontaminants. <strong>The</strong> regener<strong>at</strong>ed GAC is returned to the vessel and the vessel deliveredback to the plant <strong>at</strong> <strong>Harwell</strong>. No interruption to the oper<strong>at</strong>ion <strong>of</strong> HGCP is needed duringthis process, in contrast to the GAC change oper<strong>at</strong>ion on the old plant, which required ashutdown <strong>of</strong> up to five days.Overall, the replacement plant <strong>of</strong>fers the following improvements over the original plant:• Industrial safety hazards elimin<strong>at</strong>ed (no routine confined space working or working <strong>at</strong>height);• Lower energy consumption (the electricity used by HGCP is around 30% <strong>of</strong> th<strong>at</strong> usedby the original plant);• Minimal waste gener<strong>at</strong>ion (the GAC is regener<strong>at</strong>ed r<strong>at</strong>her than being sent to landfill);• Ease and flexibility <strong>of</strong> oper<strong>at</strong>ion (flows can be precisely specified for each borehole,and the plant can be monitored and oper<strong>at</strong>ed remotely via a laptop PC).LSG <strong>Groundw<strong>at</strong>er</strong> Report 7 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>HGCP became fully oper<strong>at</strong>ional in June 2007 and the original groundw<strong>at</strong>er plant wasdemolished in February 2008.During 2008, HGCP was oper<strong>at</strong>ional for over 99.5 % <strong>of</strong> the time, well above the targetfigure <strong>of</strong> 95 %. Sustained oper<strong>at</strong>ion <strong>of</strong> the plant is required to ensure containment <strong>of</strong> thecontamin<strong>at</strong>ed groundw<strong>at</strong>er. <strong>The</strong> closed contours around the WSA in both plots on Figure 5indic<strong>at</strong>e th<strong>at</strong> HGCP continues to be highly effective in maintaining hydraulic containment.<strong>The</strong> total volume <strong>of</strong> w<strong>at</strong>er tre<strong>at</strong>ed by the WSA groundw<strong>at</strong>er plants in 2008 was nearly480,000 m 3 (Figure 7). <strong>The</strong> total volume <strong>of</strong> w<strong>at</strong>er tre<strong>at</strong>ed as a result <strong>of</strong> the WSA hydrauliccontainment oper<strong>at</strong>ions since 1993 is now 5.6 million cubic metres.<strong>The</strong> total mass <strong>of</strong> contamin<strong>at</strong>ion removed by the plant during 2007 was 71 kg (Figure 7), adecrease over the figure for 2007. Contaminant concentr<strong>at</strong>ions in the w<strong>at</strong>er tre<strong>at</strong>ed byHGCP (the red lines on Figure 8) were initially higher than those for the old groundw<strong>at</strong>erplant, but have now stabilised <strong>at</strong> levels similar to those recorded in the final period <strong>of</strong>oper<strong>at</strong>ion <strong>of</strong> the original plant.Overall, groundw<strong>at</strong>er containment oper<strong>at</strong>ions have removed 5.75 tonnes <strong>of</strong> contamin<strong>at</strong>ionsince 1993, although it is important to note th<strong>at</strong> the primary role <strong>of</strong> the plant is containment<strong>of</strong> the contamin<strong>at</strong>ed groundw<strong>at</strong>er.<strong>The</strong> groundw<strong>at</strong>er containment oper<strong>at</strong>ion <strong>at</strong> the WSA plant forms part <strong>of</strong> a programme <strong>of</strong>works th<strong>at</strong> UKAEA is carrying out to tackle the contamin<strong>at</strong>ion. Other components <strong>of</strong> theprogramme include:• Excav<strong>at</strong>ion <strong>of</strong> the WSA chemical pits. This complex project was safely completed in2004.• Removal <strong>of</strong> contamin<strong>at</strong>ion from the Chalk below the pits (“Uns<strong>at</strong>ur<strong>at</strong>ed Zone<strong>Remedi<strong>at</strong>ion</strong>”) – see Section 4.• Enhancement <strong>of</strong> HGCP to facilit<strong>at</strong>e pumping <strong>of</strong> contamin<strong>at</strong>ed groundw<strong>at</strong>er from areasto the north <strong>of</strong> the WSA, where contaminant concentr<strong>at</strong>ions have reduced more slowlythan elsewhere.Oper<strong>at</strong>ion <strong>of</strong> HGCP is regul<strong>at</strong>ed by the Environment Agency (EA) under the terms <strong>of</strong> aWaste Management Licence (EA WML 86165), an Abstraction Licence (28/39/18/0097)and a Discharge Consent (CAWM.0231). During 2008/09 applic<strong>at</strong>ions were submitted totransfer these permits, and the Waste Management Licence for the closed landfill site <strong>at</strong>the Western Storage Area (EA WML 86127), from UKAEA to Research Sites Restor<strong>at</strong>ionLimited (RSRL). <strong>The</strong>se transfers were all successfully implemented by the EA to takeeffect from 2 February 2009, the d<strong>at</strong>e from which RSRL became the legal entityresponsible for these permits.LSG <strong>Groundw<strong>at</strong>er</strong> Report 8 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>Volume <strong>of</strong> groundw<strong>at</strong>er tre<strong>at</strong>ed (m3)500,000450,000400,000350,000300,000250,000200,000150,000100,00050,000Volume <strong>of</strong> groundw<strong>at</strong>er tre<strong>at</strong>ed in yearContaminant mass removed in year2,0001,8001,6001,4001,2001,000800600400200Contaminant mass removed (kg)0019931994199519961997199819992000200120022003200420052006200720082009Figure 7Annual quantities <strong>of</strong> groundw<strong>at</strong>er tre<strong>at</strong>ed and contaminant massremoved by the Western <strong>Groundw<strong>at</strong>er</strong> Plant3500030000Old <strong>Groundw<strong>at</strong>er</strong> Plant Inlet Concentr<strong>at</strong>ion (ppb)New <strong>Groundw<strong>at</strong>er</strong> Plant (HGCP) Inlet Concentr<strong>at</strong>ion(ppb)Total VOC Concentr<strong>at</strong>ion (ppb)2500020000150001000050000Jan-09Jan-08Jan-07Jan-06Jan-05Jan-04Jan-03Jan-02Jan-01Jan-00Jan-99Jan-98Jan-97Jan-96Jan-95Jan-94Figure 8Total contaminant concentr<strong>at</strong>ions in the w<strong>at</strong>er pumped into the Western<strong>Groundw<strong>at</strong>er</strong> PlantLSG <strong>Groundw<strong>at</strong>er</strong> Report 9 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>4 UNSATURATED ZONE REMEDIATION, WSAAn important component <strong>of</strong> the str<strong>at</strong>egy for managing the groundw<strong>at</strong>er contamin<strong>at</strong>ion <strong>at</strong>the WSA is the uns<strong>at</strong>ur<strong>at</strong>ed zone remedi<strong>at</strong>ion project. <strong>The</strong> uns<strong>at</strong>ur<strong>at</strong>ed zone is the part <strong>of</strong>the chalk aquifer th<strong>at</strong> lies above the w<strong>at</strong>er table (Figure 6). Several tonnes <strong>of</strong>contamin<strong>at</strong>ion are known to be trapped in this zone, and this contamin<strong>at</strong>ion will continue toact as a long-term source <strong>of</strong> groundw<strong>at</strong>er contamin<strong>at</strong>ion without remedi<strong>at</strong>ion.<strong>The</strong> removal <strong>of</strong> the wastes from the WSA disposal pits was necessary before remedi<strong>at</strong>ion<strong>of</strong> the uns<strong>at</strong>ur<strong>at</strong>ed zone could begin. Drilling boreholes through the wastes would havebeen hazardous and could have spread the contamin<strong>at</strong>ion. <strong>The</strong> pit contents were removedduring 2004.A very encouraging pilot scale study <strong>of</strong> various remedi<strong>at</strong>ion techniques was carried out <strong>at</strong>the WSA by AIG Engineering Ltd (“AIG”) in l<strong>at</strong>e 2005. <strong>The</strong> pilot scale study establishedth<strong>at</strong> a technique called soil vapour extraction (SVE), originally developed in the USA butnow widely applied in the UK, could be successfully used to remove contamin<strong>at</strong>ion fromthe uns<strong>at</strong>ur<strong>at</strong>ed zone.Figure 9 illustr<strong>at</strong>es how SVE works. Using vacuum pumps, air is drawn through cracks andfissures in the chalk via boreholes drilled into the uns<strong>at</strong>ur<strong>at</strong>ed zone. Vol<strong>at</strong>ile contaminantsare drawn out with the air, and are adsorbed onto GAC filters.In addition to the basic “cold” SVE technique, a trial was carried out <strong>of</strong> thermally enhancedvacuum extraction (TEVE). In TEVE, electrodes (shown during install<strong>at</strong>ion in Figure 10)are used to he<strong>at</strong> the rock, which can increase the clean up r<strong>at</strong>e and can also accesscontamin<strong>at</strong>ion th<strong>at</strong> would not be removed without the thermal tre<strong>at</strong>ment.As the pilot scale study was very succesful, full scale uns<strong>at</strong>ur<strong>at</strong>ed zone remedi<strong>at</strong>ion wasimplemented in 2006. Three oper<strong>at</strong>ional phases have taken place to d<strong>at</strong>e.<strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> the uns<strong>at</strong>ur<strong>at</strong>ed zone <strong>at</strong> the WSA has removed nearly 1,800 kg <strong>of</strong>chemical contaminants. This m<strong>at</strong>erial has been recovered from the rock bene<strong>at</strong>h four <strong>of</strong>the twenty-five former disposal pits. Following a review <strong>of</strong> historical d<strong>at</strong>a, and testingcarried out during the past year, it has been established th<strong>at</strong> uns<strong>at</strong>ur<strong>at</strong>ed zone remedi<strong>at</strong>ion<strong>at</strong> five further pit loc<strong>at</strong>ions has the potential to recover significant contaminant mass. Up tothree further phases <strong>of</strong> work are planned to undertake remedi<strong>at</strong>ion in these areas.It had been planed to install an impermeable cap over the whole <strong>of</strong> the WSA oncompletion <strong>of</strong> the remedi<strong>at</strong>ion works. This requirement is under review with theEnvironment Agency, because the benefits <strong>of</strong> the cap are not clear if the much <strong>of</strong> theremaining uns<strong>at</strong>ur<strong>at</strong>ed zone contamin<strong>at</strong>ion has been removed.During 2007, the WSA Uns<strong>at</strong>ur<strong>at</strong>ed Zone <strong>Remedi<strong>at</strong>ion</strong> project was approved as aTechnology Demonstr<strong>at</strong>ion Project by CL:AIRE 2 . CL:AIRE is a respected, independentnot-for-pr<strong>of</strong>it organis<strong>at</strong>ion established to stimul<strong>at</strong>e the regener<strong>at</strong>ion <strong>of</strong> contamin<strong>at</strong>ed land inthe UK by raising awareness <strong>of</strong>, and confidence in, practical and sustainable remedi<strong>at</strong>iontechnologies. A Technology Demonstr<strong>at</strong>ion Report is currently being finalised on theuns<strong>at</strong>ur<strong>at</strong>ed zone remedi<strong>at</strong>ion work <strong>at</strong> the WSA and will be published by CL:AIRE l<strong>at</strong>er thisyear.2 CL:AIRE - Contamin<strong>at</strong>ed Land: Applic<strong>at</strong>ions in Real EnvironmentsLSG <strong>Groundw<strong>at</strong>er</strong> Report 10 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>Figure 9Illustr<strong>at</strong>ion <strong>of</strong> remedi<strong>at</strong>ion techniques for the uns<strong>at</strong>ur<strong>at</strong>ed zone and zone<strong>of</strong> w<strong>at</strong>er table fluctu<strong>at</strong>ion <strong>at</strong> the Western Storage AreaFigure 10 Install<strong>at</strong>ion <strong>of</strong> conductive he<strong>at</strong>ing elements in boreholes for the TEVEsystemLSG <strong>Groundw<strong>at</strong>er</strong> Report 11 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>5 GROUNDWATER MONITORING<strong>The</strong> current groundw<strong>at</strong>er monitoring programme undertaken by RSRL <strong>at</strong> <strong>Harwell</strong> involvescollection and analysis <strong>of</strong> groundw<strong>at</strong>er samples on a quarterly basis. In April and October,a site-wide sampling programme is carried out, with samples being taken from eighty fiveboreholes. In January and July groundw<strong>at</strong>er quality is monitored in twenty sevenboreholes, mainly loc<strong>at</strong>ed close to the Western and Southern Storage Areas. Thisgroundw<strong>at</strong>er sampling is co-ordin<strong>at</strong>ed with the <strong>of</strong>f-site sampling undertaken by theEnvironment Agency (EA), so th<strong>at</strong> an overall picture <strong>of</strong> groundw<strong>at</strong>er contamin<strong>at</strong>ion in thearea is obtained.<strong>The</strong> results <strong>of</strong> the site-wide groundw<strong>at</strong>er sampling exercises carried out in April andOctober 2008 are presented in Figure 11. <strong>The</strong>se maps include d<strong>at</strong>a collected by both theEA and RSRL.For each loc<strong>at</strong>ion where a sample was obtained, a coloured symbol is shown on the map<strong>at</strong> the appropri<strong>at</strong>e loc<strong>at</strong>ion, with the following meanings:• Red symbols: these show sites where <strong>at</strong> least one <strong>of</strong> the chlorin<strong>at</strong>ed hydrocarbonswas present <strong>at</strong> concentr<strong>at</strong>ions above the relevant drinking w<strong>at</strong>er standard;• Amber symbols: these indic<strong>at</strong>e loc<strong>at</strong>ions where chlorin<strong>at</strong>ed hydrocarbons werepresent <strong>at</strong> concentr<strong>at</strong>ions below the drinking w<strong>at</strong>er standard, but above the limits <strong>of</strong>detection;• Green symbols: these show sites where no chlorin<strong>at</strong>ed hydrocarbons were detected.No notable changes were observed in trends for d<strong>at</strong>a collected in either April or October2008. In many parts <strong>of</strong> the contaminant plume, there continues to be a downward trend inconcentr<strong>at</strong>ions, albeit with considerable seasonal vari<strong>at</strong>ion.Figure 12 and Figure 13 show the vari<strong>at</strong>ions in the total concentr<strong>at</strong>ion <strong>of</strong> contaminants <strong>at</strong>two loc<strong>at</strong>ions downgradient (downstream in terms <strong>of</strong> groundw<strong>at</strong>er flow) <strong>of</strong> the WSA. <strong>The</strong>sedemonstr<strong>at</strong>e th<strong>at</strong>, although seasonal effects on contaminant concentr<strong>at</strong>ions can be seen,the overall trend <strong>at</strong> these loc<strong>at</strong>ions is downwards. This is because hydraulic containmenthas prevented contamin<strong>at</strong>ed groundw<strong>at</strong>er from moving away from the WSA.Following discussions with the EA, additional monitoring boreholes will be drilled during2009/10. <strong>The</strong>se will be used to refine the conceptual model to the east <strong>of</strong> the <strong>Harwell</strong> site.LSG <strong>Groundw<strong>at</strong>er</strong> Report 12 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>April 2008October 2008Figure 11 Total contaminant concentr<strong>at</strong>ions (CHCs - chlorin<strong>at</strong>ed hydrocarbons),April and October 2008LSG <strong>Groundw<strong>at</strong>er</strong> Report 13 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>45004000Western <strong>Groundw<strong>at</strong>er</strong> PlantCommissionedHWS1Concentr<strong>at</strong>ion (parts per billion)3500300025002000150010005000Jan-10Jan-09Jan-08Jan-07Jan-06Jan-05Jan-04Jan-03Jan-02Jan-01Jan-00Jan-99Jan-98Jan-97Jan-96Jan-95Jan-94Jan-93Jan-92Figure 12 Vari<strong>at</strong>ion in total contaminant concentr<strong>at</strong>ion with time in borehole HWS1(150 metres north <strong>of</strong> the WSA)80007000Western <strong>Groundw<strong>at</strong>er</strong> PlantCommissionedBorehole HWS10: Total contaminant concentr<strong>at</strong>ionConcentr<strong>at</strong>ion (parts per billion)6000500040003000200010000Jan-10Jan-09Jan-08Jan-07Jan-06Jan-05Jan-04Jan-03Jan-02Jan-01Jan-00Jan-99Jan-98Jan-97Jan-96Jan-95Jan-94Jan-93Jan-92Figure 13 Vari<strong>at</strong>ion in total contaminant concentr<strong>at</strong>ion with time in boreholeHWS10 (200 metres southeast <strong>of</strong> the WSA)LSG <strong>Groundw<strong>at</strong>er</strong> Report 14 March 2009


<strong>The</strong> <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> <strong>Chemical</strong> <strong>Groundw<strong>at</strong>er</strong> <strong>Contamin<strong>at</strong>ion</strong> <strong>at</strong> <strong>Harwell</strong>6 SUMMARY• <strong>The</strong> groundw<strong>at</strong>er containment plant (HGCP) continues to maintain effective hydrauliccontainment <strong>at</strong> the WSA. This was confirmed by the w<strong>at</strong>er level measurements madeduring 2008.• HGCP has realised improvements over the original plant in terms <strong>of</strong> health and safety,energy consumption, waste gener<strong>at</strong>ion and ease and flexibility <strong>of</strong> oper<strong>at</strong>ion. Energyconsumption is 30% <strong>of</strong> th<strong>at</strong> used by the old groundw<strong>at</strong>er plant.• <strong>Remedi<strong>at</strong>ion</strong> <strong>of</strong> the uns<strong>at</strong>ur<strong>at</strong>ed zone <strong>at</strong> the WSA has continued during 2008, removinga further 795 kg <strong>of</strong> contaminants. <strong>The</strong> total removed by the uns<strong>at</strong>ur<strong>at</strong>ed zone project isnow nearly 1.8 tonnes. Up to three further phases <strong>of</strong> uns<strong>at</strong>ur<strong>at</strong>ed zone remedi<strong>at</strong>ion areplanned.• <strong>The</strong> total mass <strong>of</strong> contamin<strong>at</strong>ion removed by the different components <strong>of</strong> theremedi<strong>at</strong>ion programme to d<strong>at</strong>e is summarised in Figure 14.Cumul<strong>at</strong>ive VOC Mass Removed (kg)1200011000100009000800070006000500040003000TotalSVE/TEVEWestern <strong>Groundw<strong>at</strong>er</strong> PlantSSA PitsWSA PitsSouthern <strong>Groundw<strong>at</strong>er</strong> Plant200010000Pre-941994/951995/961996/971997/981998/991999/002000/012001/022002/032003/042004/052005/062006/072007/082008/09Figure 14 Summary <strong>of</strong> contaminant mass removal by yearLSG <strong>Groundw<strong>at</strong>er</strong> Report 15 March 2009

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