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NATO/CCMS Pilot Study Evaluation of Demonstrated and ... - CLU-IN

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<strong>NATO</strong>/<strong>CCMS</strong> <strong>Pilot</strong> Project on Contaminated L<strong>and</strong> <strong>and</strong> Groundwater (Phase III) January 2001<br />

2. BACKGROUND/SITE DESCRIPTION<br />

From 1952 to 1985, a chemical factory was located on an area <strong>of</strong> about 10,000 m² in a city in the Ruhr<br />

area. Mostly solvents, like hydrocarbons, volatile chlorinated hydrocarbons, PAHs, petroleum, turpentine<br />

oil substitute, ketones, monoethyleneglycol, <strong>and</strong> alcohols were h<strong>and</strong>led, stored, <strong>and</strong> processed. Today, a<br />

residential building is left on the site while underground <strong>and</strong> above ground tanks are demolished.<br />

The ground was filled up 2.0 m over silty soil (approx. 4 to 11 m thick). Below the silt, a layer <strong>of</strong> s<strong>and</strong><br />

<strong>and</strong> gravel (0.8 to 7.4 m) <strong>and</strong> marly s<strong>and</strong>s (7.0 to 16.3 m below the top) have been detected. The marly<br />

s<strong>and</strong>s are the first waterpro<strong>of</strong> layer.<br />

The first aquifer is about 1.0 to 3.2 m thick <strong>and</strong> the flow velocity is very slow (kf = 6.6 ⋅ 10 -6 m/s). The<br />

concentrations <strong>of</strong> main contaminants in groundwater are petrol hydrocarbons 23.6 mg/l to 164.0 mg/l,<br />

volatile chlorinated hydrocarbons 27.0 mg/l <strong>and</strong> aromatic hydrocarbons 153.0 mg/l. Furthermore, higher<br />

concentrations <strong>of</strong> manganese <strong>and</strong> iron are present.<br />

The project is funded by the city <strong>of</strong> Essen <strong>and</strong> the state; Nordrhein-Westfalen, the former owner, went<br />

bankrupt.<br />

3. DESCRIPTION OF THE PROCESS<br />

The pilot plant was fed with groundwater, which was pumped directly from the aquifer into the front<br />

column. Two dosing pumps located behind a gravel bed in the front column fed groundwater into<br />

columns 1 <strong>and</strong> 2. The gravel filter served to hold back sediments as well as to eliminate iron <strong>and</strong><br />

manganese.<br />

• Column 1 contained:<br />

- 45 cm gravel filter (size: 2 to 3.15 mm)<br />

- 5 cm activated carbon ROW 0.08 supra<br />

- 5 cm gravel filter (gravel size: 2 to 3.15 mm)<br />

- 65 cm activated carbon ROW 0.08 supra<br />

The thickness <strong>of</strong> the activated carbon bed in Column 1 corresponded to the recommended thickness<br />

<strong>of</strong> the activated carbon bed <strong>of</strong> the adsorbent wall in the feasibility study.<br />

• Column 2 contained:<br />

- 100 cm activated carbon ROW 0.08 supra<br />

The treated water was led via an overflow into a trough located outside the container.<br />

Groundwater analyses were based on the contamination at the site; their scope was determined by the<br />

feasibility study to install an adsorbent wall. The analyses covered field parameters, general parameters<br />

<strong>and</strong> parameters to quantify BTEX <strong>and</strong> volatile CHC contamination.<br />

The analyzed general parameters included sum parameters for organic compounds as well as the<br />

parameters iron <strong>and</strong> manganese. A sum parameter for organic compounds was used in order to study<br />

whether it could serve as a substitute for analyses <strong>of</strong> individual substances. Moreover, the sum parameters<br />

were also used to check whether the results <strong>of</strong> individual analyses were plausible. Iron <strong>and</strong> manganese<br />

contents were determined in order to check whether precipitation <strong>of</strong> these substances would block the<br />

adsorbent wall.<br />

Separate analyses were carried out for BTEX <strong>and</strong> volatile CHC. The number <strong>of</strong> analyzed parameters (16)<br />

was deliberately large so as to also cover important decomposition products such as vinyl chloride.<br />

Contaminant retention by the activated carbon was determined in two ways. First, contaminant<br />

concentrations were continuously monitored at the inlet, in the columns, <strong>and</strong> at the column outlets.<br />

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