Contaminated Land Throughout the UK there are thousands of sites which have been contaminated by previous industrial use, often associated with traditional processes which are now obsolete, which may present a hazard to the general environment, but for which there is a growing requirement for reclamation and redevelopment. Recent targets set by the Government demand that 60% of all new houses should be built on "Brownfield" sites to relieve the pressure on greenfield sites and preserve the countryside. The Environment Agency estimates that some 300,000+ hectares of land are affected, covering between 5,000 and 20,000 "problem sites". The problems of contaminated land have been tackled almost exclusively in the context of redevelopment where there was the objective of economic benefit linked to environmental enhancement. The Environmental Protection Act 1990 Part IIA (inserted by Section 57 of the Environment Act, enacted April 2000) defines Contaminated land as “Any land which appears to the local authority in whose are it is situated to be in such a condition, by reasons of substances in, on or under the land, that (a) significant harm is being caused, or there is a significant possibility of such harm being caused, o (b) pollution of controlled waters is being, or is likely to be caused.” In practice less that 15% of redevelopment land will come under this definition within the UK. However with Government initiatives to reuse derelict industrial land (brown field sites) for housing and offices, many sites will be contaminated to such a level that planning restrictions will be placed on the land although it does not fit the legal definition of contamination. Many sites will contain contamination levels above published guidelines that need cleaning up in order to build upon, but are not causing, or likely to cause “significant harm”. Such sites will form 85% of land requiring remedial works for contamination and will be dealt with by standard planning procedures with no recourse to the Environment Act. Types of Contamination Potential hazards This list is by no means exhaustive, but it gives a flavour of the different classes of potential hazards. Toxic, flammable and explosive gases acetylene hydrogen cyanide hydrogen sulphide Flammable liquids and solids fuel oils solvents Combustible materials timber ash coal residues Corrosive substances acids alkalis Toxic substances phytotoxic heavy-metals hydrocarbons inorganic salts asbestos Substituted Aromatic compounds PCBs dioxins furans Biological agents anthrax tetanus BSE Genetically Modified Organisms Genetically Modified Pollens UK Approach The problems of contaminated land in the UK have been tackled almost exclusively in the context of redevelopment where there was the objective of economic benefit linked to environmental enhancement. This has lead to an approach based around the ‘suitability for use’ concept and evaluated in terms of risk assessment. Section 57 of the 1995 Environment Act endorses the risk based approach for managing contaminated land and adopts a rationale based on international definitions toxicity – potential of a material to harm biological systems hazard - the nature of the adverse effect posed by the compound risk – the probability of suffering harm or loss under specific circumstances. A risk therefore only exists where there is a Contaminant or Source which can reach a Receptor via a Pathway This can be done in a QUALITATIVE or QUANTITATIVE way Sources of Contamination Gasworks Coal tar creosote Phenols phenol Cyanide free / complex Sulphur sulphide / sulphate Iron + Steel works Metals copper, nickel, lead Acids sulphuric, hydrochloric Mineral oils Coking works residues (as for gasworks ) Metal finishing Metals cadmium, chromium, copper, nickel, zinc Acids sulphuric, hydrochloric Plating salts cyanide Aromatic hydrocarbons benzene Chlorinated hydrocarbons 1,1,1-Trichloroethane Non ferrous metal processing Metals copper, cadmium, lead, zinc Impurity metals antimony, arsenic Other wastes battery cases, acids Oil refineries Hydrocarbons various fractions Acids, alkalies sulphuric, caustic soda Lagging, insulation asbestos Spent calalysts lead, nickel, chromium Paints Metals lead, cadmium, barium Alcohols toluol, xylol Chlorinated hydrocarbons Methylene Chloride Fillers, extenders silica, titanium dioxide, talc Petrochemical plants Acids, alkalies sulphuric, caustic soda Metals copper, cadmium, mercury Reactive monomers styrene, acrylate, VCM Cyanide toluene di-isocyanate Amines analine Aromatic hydrocarbons benzene, Toluene Petrol stations Metals copper, cadmium, lead, nickel, zinc Aromatic hydrocarbons benzene Octane boosters lead, MTBE Mineral oil - Chlorinated hydrocarbons trichloroethylene Paint, plastic residues barium, cadmium, lead Rubber processing Metals zinc, lead Sulphur compounds sulphur, thiocarbonate Reactive monomers isoprene, isobutylene Acids sulphuric. hydrochloric Aromatic hydrocarbons xylene, Toluene Pathway Pathways can exist via air, water and soil. This can be by ingestion, inhalation, eye contact, absorption through skin, contamination of plants and animals, uptake by vegetation, drinking water contaminated or migration through permeable strata. This relates to several factors, such as: the nature of the site (physical layout and geology). the nature of the use and exposures the nature of the pollutants The nature of the pollutants can include: Pollutant solubility: will determine how much dissolves into water Pollutant volatility: will determine how much passes into the air. Pollutant partitioning and adsorption: will determine how strongly it is held to solids. This can mean that a site with, for example, a range of organic pollutants may have a variety of different pathways. Transport Properties of Selected Organic Contaminants Compound Benzene Phenol Hexachlorodibenz ene-p-dioxin Benzo[a]pyrene Aqueous Solubility (mg/l) 1780 8.2x104 1.3x10-4 Vapour pressure (Pa) 1.3x104 71 1.9x10-6 Koc* 65 14 2.6x107 Dominant partition medium Air Water Soil 3.8x10-3 7.3x10-7 5.5x106 Soil * partitioning coefficient organic carbon-water Receptors and Targets The receptors can be: People Water Resources Flora and Fauna Buildings adults, children, site workers, residents, visitors, neighbours surface, ground SSSIs, livestock, wild animals, birds, landscaping foundations, services, structures Defined in EPA 1990 Sensitivity of use: Domestic Gardens Allotments Parks Landscaped Areas Buildings (no gardens) Hard Covered Areas Most Sensitive Least Sensitive Risk Assessment see handout Standards Once a risk has been identified, it needs to be quantified. Inter Departmental Committee on the Reuse of Contaminated Land ICRCL 59/83 Trigger Concentrations Contaminant Planned Use Group A (may pose hazards to health) Arsenic Domestic gardens, allotments Parks, playing fields, open space Cadmium Domestic gardens, allotments Parks, playing fields, open space Domestic gardens, allotments Chromium (hexavalent) (1) Parks, playing fields, open space Domestic gardens, allotments Chromium (total) Parks, playing fields, open space Lead Domestic gardens, allotments Parks, playing fields, open space Mercury Domestic gardens, allotments Parks, playing fields, open space Selenium Domestic gardens, allotments Parks, playing fields, open space Group B (Phytotoxic - but not normally hazardous to health) Boron Any uses where plants are grown (2) (6) (water-soluble) (3) Copper (4) (5) Any uses where plants are grown (2) (6) Nickel (4) (5) Any uses where plants are grown (2) (6) Zinc (4) (5) Any uses where plants are grown (2) (6) Group C - (Organic contaminants) Domestic gardens, allotments, play areas Polyaromatic hydrocarbons (7) (8) Landscaped areas, buildings, hard cover Phenols Domestic gardens, allotments, Landscaped areas, buildings, hard cover Cyanide Domestic gardens, allotments, landscaped (free) areas Buildings, hard cover Cyanide Domestic gardens, allotments (complex) Landscaped areas Buildings, hard cover Thiocyanate All proposed uses Sulphate Domestic gardens, allotments, landscaped areas Buildings (9) Hard cover Sulphide All proposed uses Sulphur All proposed uses Acidity Domestic gardens, allotments, landscaped areas Buildings, hard cover Trigger Values (mg / kg air-dried soil) Threshold Action 10 40 3 15 25 No Limit No Limit 600 1,000 500 2,000 1 20 3 6 Threshold Action 3 130 70 300 Threshold Action 50 500 1,000 10,000 5 200 5 1,000 25 500 100 250 250 250 50 500 1,000 5,000 No Limit No Limit 2,000 10,000 2,000 2,000 250 5,000 50,000 No Limit 1,000 20,000 pH<5 pH<3 No Limit No Limit The New Dutchlist Contaminant Metals Arsenic Barium Cadmium Chromium Cobalt Soil Sediment(mg/kg dry weight) optimum action 29 200 0.8 100 20 Groundwater(µg/l) optimum 55 625 12 380 240 action 10 50 0.4 1 20 60 625 6 30 100 Copper Lead Molybdenum Nickel Mercury Zinc Cyanides Free Complex (pH<5) (1) Complex (pH>5) (1) Thiocyanate Aromatics Benzene Ethylbenzene Phenol Toluene Xylene Cresol Catechin Resorein Hydroquinone Polycyclic Aromatic Hydrocarbons (PAH) Anthracene Benzo(a)pyrene Fluoroanthrene Naphtalene Phenanthrene Benzo(a)anthracene Chrysene Benzo(a)fluoranthrene Benzo(k)fluoranthrene Benzo(g,h,i)perylene Indenol(1,2,3-c,d)pyrene Total PAH (2) (10) Chlorinated Hydrocarbons 1,2 Dichloroethane Dichloromethane Tetrachloromethane Tetrachloroethane Trichloromethane Trichloroethene Vinylchloride Monochlorobenzene Dichlorobenzol (total) Trichlorobenzol (total) Tetrachlorobenzol (total) Pentachlorobenzene Hexachlorobenzene Chlorobenzenes (3) (10) Monochlorophenol Dichlorophenol Trichlorophenol Tetrachlorophenol Pentachlorophenol Chlorophenols (total) (4) (10) Chloronapthylene PolyChloroBiphenyls (total)(5) (10) Pesticides DDT/DDD/DDE (total) (6) Aldrin Dieldrin Endrin Drins (total) alpha HCH 36 85 10 35 0.3 140 optimum 190 530 200 210 10 720 action 1 5 5 - optimum 20 650 50 - optimum action 0.05[d] 0.05[d] 0.05[d] 0.05[d] 0.05[d] optimum action ---1 optimum action [d] 0.001 0.01 0.001 0.001 [d] 0.01 0.01 0.01 0.0035 0.0025 0.0025 0.003 0.001 0.001 0.002 0.02 optimum 75 75 300 75 0.3 800 action 5 10 10 20 optimum 2 50 40 130 25 5[d] 20 10 10 1500 1500 1500 1500 action 0.2 0.2 0.2 0.2 0.2 - 4 20 1 4 10 60 0.1 30 5 10 10 1 4 [d] 4 - action 0.02 0.001 0.005 0.1 0.03 0.002 0.002 0.003 0.001 0.0002 0.0004 optimum action 30 150 2000 1000 70 200 1250 600 800 optimum 40 action 0.0025 0.0025 0.0005 0.001 0.0025 15 15 5 15 0.05 65 5 0.5 1 70 5 0.5 0.05 0.5 0.05 0.05 0.05 - 0.01[d] 400 0.01[d] 1000 0.01[d] 10 0.01[d] 40 0.01[d] 400 0.01[d] 500 0.7 0.01[d] 180 0.01[d] 50 0.01[d] 10 0.01[d] 2.5 0.01[d] 1 0.01[d] 0.5 0.25 100 0.08 30 0.025 10 0.01 10 0.02 3 6 0.01 0.01[d] optimum action [d] 0.01 [d] 0.02ng/l 0.1 [d] - beta HCH gamma HCH HCH combined (7) Carbaryl Carbofuran Maneb Atrazin Miscellaneous Tetrahydrofuran Pyridine Tetrahydrothiophene Cyclohexanone Styrene Mineral Oil (9) Phthalates (total) 0.001 0.05 µg/l 0.05 µg/l optimum action 0.1 0.1 0.1 0.1 0.1 50 0.1 2 5 2 35 6 0.4 1 90 270 100 5000 60 [d] 0.2 ng/l 1 0.01[d] 0.1 0.01[d] 0.1 [d] 0.1 0.0075 150 optimum action 0.5 1 0.5 3 0.5 30 0.5 15000 0.5 300 50 600 0.5 5 Kelly Indices (Former GLC) Guidelines for Contaminated Soils specifically developed for gasworks sites in London: Suggested Range of Values (mg/kg on air-dried soils, except for pH) Uncontamin ated pH (acid) 6-7 pH (alkaline) 7-8 Antimony 0-30 Arsenic 0-30 Boron (available) 0-2 Barium 0-500 Beryllium 0-5 Cadmium 0-1 Chromium 0-100 Copper 0-100 (available) Cyanide (free) 0-1 Cyanide 0-5 Ferricyanide 0-100 Lead 0-500 Lead (available) 0-200 Mercury 0-1 Manganese 0-500 Magnesium 0-500 Nickel 0-20 (available) PAHs (Coal Tar) 0-500 Phenol 0-2 Selenium 0-1 Sulphate 0-2000 Sulphur (free) 0-100 Sulphide 0-10 Thiocyanate 0-10 Toluene extract 0-5000 Vanadium 0-100 Zinc (available) 0-250 Zinc (equivalent) 0-250 Parameter Slight Contamin Heavy Contamination ated Contamination 5-6 4-5 2-4 8-9 9-10 10-12 30-50 50-100 100-500 30-50 50-100 100-500 2-5 5-50 50-250 500-1000 1000-2000 2000-1.0% 5-10 10-20 20-50 1-3 3-10 10-50 100-200 200-50 500-2500 100-200 Unusually Heavy Contamination <2 > 12 > 500 > 500 > 250 > 1.0% > 50 > 50 > 2500 200-500 500-2500 > 2500 1-5 5-50 5-25 25-250 100-500 500-1000 500-1000 1000-2000 200-500 500-1000 1-3 3-10 500-1000 1000-2000 500-1000 1000-2000 50-100 250-500 1000-5000 200-10,000 1000-5000 10-50 2000-10,000 2000-1.0% > 100 > 500 > 5000 > 10,000 > 5000 > 50 > 10,000 > 1.0% 50-200 200-1000 > 1000 500-1000 1000-2000 2-5 5-50 1-3 3-10 2000-5000 5000-1.0% 100-500 500-1000 10-20 20-100 10-50 50-100 5000-1.0% 1.0-5.0% 100-200 200-500 250-500 500-1000 250-500 500-2000 2000-1.0% 50-250 10-50 1.0%-5.0% 1000-5000 100-500 100-500 5.0-25.0% 500-2500 1000-5000 2000-1.0% > 1.0% > 250 > 50 > 5.0% > 5000 > 500 > 500 > 25.0% > 2500 > 5000 > 1.0% 20-50 Contaminated Land Research Programme On the 14th of March 2002, the first result of a 10-year project to create standard procedures for risk assessment in the UK were released by the EA and DEFRA in a series of documents. This included a mathematical model for Contaminated Land Exposure Assessment (CLEA). This also included the first 7 (out of 55) of the Tox series of reports were released giving Soil Guideline Values for Arsenic, Cadmium, Chromium, inorganic Mercury, Nickel, Selenium and Lead. These have only been available since 22nd of April and can be found for download at http://www.defra.gov.uk/. Sampling Sampling of contaminated sites has always been difficult because of the potential for ‘hot spots’ giving an uneven spread of pollution. As certain chemical analyses can be quite expensive there has always been a trade off between the number of samples and the probability of finding a randomly located source. This can be explained statistically by assuming the distribution of pollution is random according to a frequency distribution. Sampling is usually arranged in a grid (effectively stratified random sampling) BS DD175: Guidance on the Number of Sampling Points Area (Ha) of Site Recommended Number Sampling Points 0.5 1.0 5.0 15 25 85 of Implied Spacing 18 m 20 m 24 m Area (m2) of contamination to give detection (95% confidence) 905 1129 1732 BS DD171 also recommends that samples are taken at 3 depths (surface, max excavation + 1 intermediate) or every 0.5 m. ICRCL recommends that at small sites a 10-15 m grid is used and on large sites a 2550m. The grid represents the are of contamination which could be handled without difficulty if not found during the investigation. Further statistical guidance has been issued as part of the Contaminated Land Exposure Assessment document series. Soil, water and air samples can be taken for analysis as required from boreholes or trial pits. If the previous use has been well documented, sampling can be targeted at known problem areas, such as tar storage areas Stages of Site Investigation Phased investigation. I. II. III. Phase 1 investigation. Gathering existing information. identify sources, receptors and pathways Phase 2 – risk estimation and evaluation. Estimation involves quantifying the nature and extent of exposure of the receptors and the magnitude of effects should exposure occur. This requires a physical investigation of the site and the pollutant levels. The compounds, their concentrations and receptors are identified and are usually related to the ICRCL or Dutch environmental standards. The evaluation of this risk is then made against the probability and consequence of the exposure to decide how the risk will be managed. The next stage is the remediation or site management IV. Final - check levels following clean up. Generally to be below Target or Threshold value. Design details can be found in Cairney and Hobson, 1998 Remediation Options Technologies to control remediate contaminated sites depend on the type of pollutant and site. Biodegradable pollutants organic can be removed by breakdown by microorganisms. Other pollutants can be selectively removed from the soil and others can be immobilised. This can include: Removal of material for treatment and disposal as a hazardous waste Containment: this limits the mobility of material and blocks the pathway to the receptor. Treatment: biological, chemical and physical processes to treat the contamination. Excavation and Disposal Traditionally this was the most common method of remediating contaminated sites with about 1x106 m3 of contaminated soil being buried per year. However, new landfill regulations and the landfill tax have limited this option. Containment Cover Systems: a layer (or layers) are used to cover the contamination. This can be to just put distance between with contamination and the surface, or an impermeable material to seal the site from water (i.e. to stop precipitation contaminating groundwater) or protect occupants from gas venting. This can be used for a wide range of contamination. Designs are made on a site specific basis and are usually made up of gravel, geotextiles and clays of specified engineering properties. In-Ground Barriers: these isolate a contaminated mass of ground from the environment. This can be above, below or around the material. Materials include clays, clay-bentonite slurry walls, membranes and sheet piles. The design of in ground barriers depends on the site conditions and the phase of the contamination. gas water aquiclude a) standard cut-off water aquiclude b) membrane barrier gas water aquiclude c) gas / leachate barriers organics water d) light organics barrier Bioremediation Bioremediation: this uses biological processes (mainly micro-organisms) to degrade organic pollutants. This of course needs the right ‘bugs’ in the right conditions. Phytoremediation involves growing plants on the site to either promote rhizosphere degradation processes or promote uptake of compounds such as heavy metals. This can be done ex-situ, where the material is dug and then either placed in a bioreactor or in windrows to promote aeration. It is estimated that about 100-200 sites have been remediated in this way in the UK. In-situ bioremediation has been applied to about 30 sites in the UK. It involves stimulating degradation by seeding with microbes and/or modifying physical conditions in the ground. This can be as in bio-venting where air is introduced to promote biological activity or by adding nutrients and/or substrates to stimulate biological activity. See Handout. Physical Processes Vapour extraction/air sparging can be used to remove volatile compounds from the vapour space in soils. Various techniques have been applied to achieve this at about 400 sites in the UK. Air flow is stimulated by withdrawing or introducing air into the soil causing volatile compounds to pass into the vapour phase Dual Phase extraction: this involves removing air and water from the site to extract volatile and water soluble compounds. Soil washing involves extracting the soil and washing it with water or other chemicals. It has been applied to organic and heavy metal contamination. Cement fixation, this involves fixing pollutants (particularly heavy metals) with cement or other compounds which bind up the material. 10 projects in the UK have used this technology, either by injecting material into the ground or by extracting the soil and mixing with cement on the surface. This effectively ‘locks’ up the contaminants and prevents a pathway to a receptor being established. See Handout Case Studies Lumsden Road, Portsmouth 120 families rehoused after houses, built in the 1950s and 1960s, were found to be on an old RN waste site contaminated with asbestos and heavy metals. The rehousing, medical screening, demolition, remediation and rebuilding cost £6.12m. Clarke Avenue, Loscoe, Derbyshire bungalow demolished and occupants injured by exploding landfill gas £350k Ilford Essex, late 1980s, low level radiation found on former chemical works being redeveloped for housing. Remediation and delays cost £10m. http://www.contaminatedland.co.uk/case-stu/erg-finy.htm References Cairney, T and Hobson, D.M. 1998. Contaminated Land, problems and solutions. E and FN Spon Evans, D., Jefferies, S.A, Thomas and Cui, S. 2001. Remedial processess for Contaminated Land. CIRIA Report C549, CIRIA London. Rudland, D.J., Lancefield, R.M. and Mayell, P.N. 2001. Contaminated Land Risk Assessment. CIRIA Report C552, CIRIA, London. Hester, R.E. and Harrisson, R.M. 1997. Contaminated Land and its Reclamation. Royal Society of Chemistry, London. Web sites DETR EA + various
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