1                                  Introduction

1.1                            Background to the Study

The Castle Peak Power Company (CAPCO) has initiated a project for emission control at the Castle Peak Power Station “B” units (CPB) (“Project”), in response to the Hong Kong SAR Government (HKSARG)’s stated intent to reduce emissions in Hong Kong.  An Environmental Impact Assessment (EIA) Study Brief was issued for the Project by the Environmental Protection Department (EPD) in October 2005 (EIA Study Brief No. ESB-134/2005).  In compliance with one of the Study Brief requirements, a land contamination assessment will be carried out for the Project Areas.

To accommodate the new development, extensive demolition works are required to relocate a number of existing facilities, including:

·       CPB Fuel Oil Day Tank (FODT, hereafter referred to as the aboveground fuel oil day tank) and associated pipe works connecting with fuel oil pump house (FOPH) and oil interceptor;

 

·       Dangerous Goods (DG) stores; and

 

·       Intermediate Pressure Reduction Station (IPRS), LPG compound and CO2 storage tanks.

The preliminary Project Areas are shown in Figure 1.1a of the approved CAP (Annex E1a).

Environmental Resources Management (ERM) was commissioned by CAPCO to conduct a land contamination assessment of the site, in accordance with the Study Brief requirements.  A Contamination Assessment Plan (CAP) was prepared, submitted to and was approved by the EPD (Annex E1a) and forms a basis of this assessment.

Site inspection including soil and groundwater sampling and analysis was conducted to identify potential sources of contamination from historical and on-going operations in this area in accordance with the CAP.

1.2                            Objectives of the Land Contamination Assessment

The main objectives of the land contamination assessment were to establish the presence or absence of soil and groundwater contamination and, if present, the degree of contamination.

1.3                            Scope Of The Land Contamination Assessment

The scope of the assessment included the following:

·       to review the available history of the site in relation to the potential for land contamination;

·       to review the available geology and hydrogeology information of the site;

·       to conduct a site investigation programme through soil and groundwater sampling at twelve strategic locations;

·       to perform laboratory analyses of soil and groundwater samples for the target analytical parameters; and

·       to report on the findings of the available information, the field observations, the interpretation of laboratory analytical results, and the assessment of potential contamination.

1.4                            Structure Of The CAR

The remainder of this report is structured as follows:

·       Section 2 summarises the background information, including historical land uses, geology, hydrogeology and the results of previous investigations at the site, if any;

·       Section 3 summarises the methodology used to carry out the land contamination assessment;

·       Section 4 summaries the field activities and field observations;

·       Section 5 presents the laboratory analytical results for the samples collected; and

·       Section 6 provides the conclusions and recommendations.

Annexes to this report include:

·       Annex    E1a   Contamination Assessment Plan

·       Annex    E1b   Borehole Logs

·       Annex    E1c   Groundwater Monitoring Well Diagrams

·       Annex    E1d   Selected Photographs

·       Annex    E1e   Laboratory Analytical Results

·       Annex    E1f    The Dutch List

 

2                                  background

2.1                            Site Description

The Project Areas are located within the CPB, situated on the coast of Tap Shek Kok in Tuen Mun, New Territories.

The Castle Peak ”B” station was commissioned between 1985 and 1989.  The area of this land contamination assessment covers the proposed Project Areas, including part of the northern coal storage yard, fuel oil day tank (FODT), dangerous goods (DG) stores, intermediate pressure reduction station (IPRS), LPG compound, CO2 storage tanks and a proposed area for proposed gypsum dewatering and storage facilities located within the western coal storage yard.  These facilities are presented in Figure 1.1a of the approved CAP (Annex E1a).

The coastline is located approximately 350 to 500 meters to the south and southwest of the Project Areas.  The direction of groundwater flow underlying the Project Areas is anticipated to be affected by the nearby tidal motion and groundwater is likely to be recharged by seawater during high tides and discharged to the sea during low tides. 

Groundwater is not used for either domestic or industrial purposes at the site or the adjacent areas.

2.2                            Surrounding Land Use

The land uses in the immediate surroundings of the Project Areas include:

North: The power generation units of Castle Peak Power Station “A” (CPA);

South: The north coal yard, the coastline is located approximately 350 m to the south;

East: The power generation units of CPB and Green Island Cement Plant; and

West: The west coal yard, the coastline is approximately 500 m to the west.

 

3                                  methodology

The site investigation programme was designed in accordance with the Environmental Protection Department (EPD)’s Practice Notes for Professional Persons: Contaminated Land Assessment and Remediation ProPECC PN 3/94 (ProPECC PN3/94) and Guidance Notes for Investigation and Remediation of Contaminated Sites of Petrol Filling Stations, Boatyards, and Car Repair/Dismantling Workshops (Guidance Notes).

3.1                            Soil Contamination Assessment

The soil contamination assessment was carried out through analysis of soil samples collected from strategic locations at different depths in accordance with the EPD-approved CAP.  Soil sampling was conducted through soil excavation or intrusive soil drilling in accordance with the American Society for Testing and Materials’ (ASTM) standards ([1]).

3.2                            Groundwater Contamination Assessment

The groundwater contamination assessment was carried out through the analysis of groundwater samples collected from eight groundwater sampling wells.  Groundwater well installation, well development and sampling were carried out following the guidance for groundwater sampling developed by USEPA for groundwater contamination investigation ([2]).

3.3                            Laboratory analysis

The methodologies used for the laboratory analysis were as follows:

·       Total petroleum hydrocarbons (TPH) for soil and groundwater samples by USEPA Method 8260 & 8015;

·       benzene, toluene, ethylbenzene, xylene (BTEX) for soil and groundwater samples by USEPA Method 8260;

·       polycyclic aromatic hydrocarbons (PAHs) for soil and groundwater samples by USEPA Method 8270;

·       Volatile organic compounds (VOCs) for soil and groundwater samples by USEPA Method 8260; and

·       Semi-volatile organic compounds (SVOCs) for soil and groundwater samples by USEPA Method 8270.

 

4                                  Field activities and observations

4.1                            Field Activities

4.1.1                      Underground Soil boring and Sampling

Hand excavation and soil sampling was carried out at four trial pits.  Soil boring and sampling were carried out at eight drilling locations.  The trial pits were excavated manually, and soil boring was conducted using rotary drilling rigs.  The approximate locations of trial pits and boreholes are shown on Figure 3.1a of the approved CAP (Annex E1a).

Soil samples were collected from the trial pits and boreholes at designated depths for visual inspection on the soil geological classification and signs of contamination, on-site photo-ionisation detector (PID) testing for volatile organic compound vapour and laboratory analysis.  Soil sampling at the trial pits was performed manually using a stainless steel scoop.  Soil sampling in the boreholes was conducted using split barrels following the standard penetration testing (SPT) procedures.  Of note is that no soil sample was collected from the depths where hard strata (ie boulders, cobbles or bedrock) were encountered during the drilling or sampling.  A summary of the soil boring and sampling works is provided in Table 4.1a. 

The four trial pits TP1, TP2, TP3 and TP4 were located near the boring locations DH7, DH6, DH5 and DH4, respectively, and were excavated to depths between 0.7 and 1.5 m bgl.  Soil sampling for the depths near the ground surface (ie 0.5 to 1.0 m bgl) was not carried out at boreholes DH4 to DH7 but at the trial pits TP1 to TP4 instead.

Table 4.1a      Soil Boring and Sampling for the Land Contamination Assessment

Locations

Total drilling depth

(m bgl)

Collected soil sample for PID testing and laboratory analysis

 (m bgl)

Remarks

DH1

6.27

DH1 0.6 m

Boulder/cobble/rock encountered from depth 0.6 to 6.27 m bgl.

DH2

6.77

DH2 0.6 m

Boulder/cobble/rock encountered from depth 1.0 to 6.77 m bgl.

DH3

7.07

DH3 0.8 m

Cobble/granite encountered from depth 1.9 to 7.07 m bgl.

DH4

6.81

No soil sample collected

Boulder/cobble/rock encountered from depth 0.25 to 6.81 m bgl.

DH5

6.80

No soil sample collected

Boulder/cobble/rock encountered from depth 0.48 to 6.80 m bgl.

DH6

7.15

No soil sample collected

Boulder/cobble/rock encountered from depth 0.6 to 7.15 m bgl.

DH7

6.77

No soil sample collected

Boulder/cobble/rock encountered from depth 1.38 to 6.77 m bgl.

DH8

7.53

DH8 0.8 m

Boulder/cobble/rock encountered from depth 1.0 to 7.53 m bgl.

TP1

1.5

TP1 1.5 m

TP1 was located near DH7.

TP2

1.1

TP2 0.8 m (a)

TP2 was located near DH6.

TP3

1.1

TP3 0.9 m

TP3 was located near DH5.

TP4

1.0

TP4 0.7 m

TP4 was located near DH4.

Note:

(a)  One soil field duplicate sample (TP2 (duplicate)) was collected from this location.

The underground soil profiles observed during the drilling were recorded are presented in the Borehole Logs, Annex E1b.

All soil samples collected from the boreholes were placed immediately into laboratory pre-cleaned sample bottles and stored with ice in a cooler on-site before delivery to the laboratory for analysis.

ERM supervised the field drilling and soil sampling to meet the requirements of the project QA/QC and appropriate decontamination procedures.

4.1.2                      Groundwater Well Installation and Sampling

Groundwater was encountered at all eight boreholes during the drilling.  The boreholes were converted into groundwater monitoring wells to facilitate groundwater sampling.  In general, groundwater monitoring wells were installed to approximately 2 m below the measured groundwater levels using perforated u-PVC pipes.  Diagrams showing details of the installed groundwater wells are provided in the Groundwater Monitoring Well Diagrams, Annex E1c.

After groundwater well installation, each well was developed by removing at least five times the well volume by hand bailing.  Groundwater samples were collected using new dedicated Teflon bailers for each well.

A total of eight groundwater samples (exclusive of QA/QC samples), marked as DH1 to DH8, were collected.  All groundwater samples collected from the wells were placed immediately into laboratory pre-cleaned and pre-preserved sample bottles and stored with ice in a cooler on-site before delivery to the laboratory for analysis.

ERM supervised the groundwater sampling to meet the requirements of the project QA/QC and appropriate decontamination procedures.

4.1.3                      QA/QC Programme and Sample Delivery

A field QA/QC program was incorporated into the land contamination investigation for the site.  The program consisted of collection of field QA/QC samples which included one soil field duplicate sample, one groundwater field duplicate sample, three equipment blank samples, and seven trip blank samples.  The field QA/QC samples collected or prepared are summarized in Table 4.1b.

Table 4.1b      Collected QA/QC Samples for the Site Investigation

QA/QC sample

Sample ID

Associated sample

Soil duplicate sample

 

TP2 (duplicate)

TP2 at 0.8m bgl

Groundwater duplicate sample

 

DH6 (duplicate)

DH6

Equipment Blank samples

EQ BLK 1

Soil samples TP1 1.5m, TP2 0.8m, TP3 0.9m, TP4 0.7m and DH9 0.8m.

 

EQ BLK 2

Soil samples DH1 0.6m and DH2 0.6m.

 

EQ BLK 3

Soil sample DH8 0.8m

Trip blank samples

Trip blank 1

Soil samples TP1 1.5m, TP2 0.8m, TP3 0.9m, TP4 0.7m and DH9 0.8m.

 

Trip blank 2

Soil samples DH1 0.6m and DH2 0.6m.

 

Trip Blank 3

Groundwater samples DH4, GH5, DH6, DH7, DH9 and soil sample DH3 0.8m.

 

Trip Blank 4

Groundwater samples DH1 and DH2.

 

Trip Blank 5

Soil samples DH8 0.8m.

 

Trip Blank 6

Groundwater sample DH3.

 

Trip Blank 7

Groundwater sample DH8.

All trip blank samples were pre-prepared in the laboratory, stored with the samples in the sample coolers, and delivered with the samples to the laboratory. 

All soil and groundwater samples along with the field QA/QC samples were delivery to the laboratory on ice in coolers on each sampling day.

4.2                            Field Observations

4.2.1                      Soil

At all land contamination investigation locations, the ground surface generally comprised yellowish brown medium to coarse sand from the ground surface to approximately 0.25 to 1.9 meters below ground level (m bgl) following by cobbles, boulders or bed rocks (granite) to the end of the drilling depths (ie 6 to 8 m bgl).

No evidence of soil contamination such as staining, discoloration or abnormal odour was observed during the soil drilling and sampling.

4.2.2                      PID Test Results

The photo-ionisation detector (PID) test results for the soil samples are summarized in Table 4.2a.

Table 4.2a     Soil Sample PID Test Results

Locations

Soil sample

(m bgl)

PID test Results

(ppm)

Remarks

TP1

TP1 1.5 m

0.8

TP1 was located near DH7

TP2

TP2 0.8 m

1.5

TP2 was located near DH6

TP3

TP3 0.9 m

1.0

TP3 was located near DH5

TP4

TP4 0.7 m

4.0

TP4 was located near DH4

DH1

DH1 0.6m

2.0

 

DH2

DH2 0.6 m

2.0

 

DH3

DH3 0.8 m

0.5

 

DH8

DH8 0.8 m

0.8

 

4.2.3                      Groundwater

The groundwater levels encountered during the drilling and measured at equilibrium condition are provided in Table 4.2b.

Table 4.2b      Groundwater Level Measured at the Monitoring Wells

Groundwater Monitoring Well

Groundwater Level Encountered During Drilling
(m bgl)

Groundwater Level Measured

at Equilibrium Condition (m bgl)

Groundwater Level Elevation
(mPD) (a)

DH1

2.38

2.38

2.67

DH2

2.55

2.55

2.57

DH3

3.70

4.19

2.81

DH4

4.70

4.70

1.31

DH5

4.62

4.76

1.25

DH6

4.60

5.00

1.23

DH7

4.72

4.72

1.95

DH8

5.50

5.51

1.56

Note:

(a)   Groundwater level elevations (meter above principal datum (mPD)) were estimated based on the ground level survey data and groundwater levels measured at equilibrium condition.

Based on the groundwater water levels measured and the local surface hydrology, the shallow groundwater in the site area is anticipated to flow in a generally southern or south-westerly direction.  However, the direction of groundwater flow underlying the site area is likely to be affected by the nearby tidal motion.

No evidence of groundwater contamination such as free floating products, discoloration or abnormal odour was observed at the sampling locations during the drilling, well development and groundwater sampling.

 

5                                  Analytical Results

The analytical results for the soil and groundwater samples collected from the Site are summarised in Tables 5.1a and 5.1b, respectively, and are discussed in the following sections.  The detailed results of the laboratory analyses along with the QA/QC information are presented in Annex E1e.

5.1                            Criteria for Assessment

The EPD’s ProPECC PN 3/94 has adopted the Dutch Ministry of Housing, Planning and Environment Soil and Groundwater Standards (the ‘Dutch List) as the criteria for assessing soil and groundwater contamination in Hong Kong.  The Dutch List was used as the reference against the analytical results for the samples.

As an initial screening tool for establishing a general understanding of the degree and extent of soil and groundwater contamination, the Dutch List defines three different levels, ie ‘A’, ‘B’ and ‘C’, for the concentration of contaminants found in soil and groundwater.  The interpretation of the contaminant concentrations is as follows:

·       Concentrations below ‘A’ and/or ‘B’ values refer to a situation in which the soil and/or groundwater is considered ‘unpolluted’ and can fulfil all possible functions and no further actions are required.

·       Concentrations above ‘B’ but below ‘C’ values refer to a situation in which the soil and/or groundwater is potentially contaminated and requires further investigation.  In Hong Kong, the Dutch ‘B’ values are currently used by the EPD as the soil cleanup target for most cases.  Soil and groundwater with contaminant concentrations exceeding such values are considered by the EPD to be contaminated and may need to be remediated to below this level.

·       Concentrations above ‘C’ are considered to represent significant contamination and cleanup action is likely to be required.

In the absence of appropriate criteria applicable to industrial use, the Dutch Intervention Values (DIVs), which are much more stringent criteria intended for groundwater abstracted for drinking purpose, are used for comparison with the measured results for substances in groundwater samples that are not included in the Dutch List adopted in EPD’s ProPECC PN 3/94.

 


Table 5.1a  Analytical Results for Soil Samples (all results in mg/ kg- dry weight) (a) (b)

Parameter

Dutch

‘A’

Dutch

‘B’

Dutch

‘C’

Report Limit

TP1

1.5 m

TP2

0.8 m (e)

TP3

0.9 m

TP4

0.7 m

DH1

0.6 m

DH2

0.6 m

DH3

0.8 m

DH8

0.8 m

Moisture Content (%)

N/A

N/A

N/A

0.1

6.9

4.5

6.6

5

10.1

8.5

7.7

4.3

TPH

 

 

 

 

 

 

 

 

 

 

 

 

Gasoline (C6-C9)

20

100

800

2

ND

ND

ND

ND

ND

ND

ND

ND

Light Diesel (C10-C14)

N/A

N/A

N/A

50

ND

ND

83

ND

ND

ND

ND

ND

Heavy Diesel (C15-C28)

N/A

N/A

N/A

50

ND

ND

1,170

ND

ND

ND

ND

ND

Heavy Oil (C29-C36)

N/A

N/A

N/A

50

ND

ND

605

ND

ND

ND

ND

ND

Mineral Oil (c)

100

1,000

5,000

N/A

ND

ND

1,858

ND

ND

ND

ND

ND

BTEX

 

 

 

 

 

 

 

 

 

 

 

 

Benzene

0.01

0.5

5

0.5

ND

ND

ND

ND

ND

ND

ND

ND

Toluene

0.05

3

30

0.5

ND

ND

ND

ND

ND

ND

ND

ND

Ethylbenzene

0.05

5

50

0.5

ND

ND

ND

ND

ND

ND

ND

ND

meta- & para-Xylene

N/A

N/A

N/A

1

ND

ND

ND

ND

ND

ND

ND

ND

ortho-Xylene

N/A

N/A

N/A

0.5

ND

ND

ND

ND

ND

ND

ND

ND

Total xylene (d)

0.05

5

50

N/A

ND

ND

ND

ND

ND

ND

ND

ND

Chlorobenzene

0.05

2

20

0.5

ND

ND

ND

ND

ND

ND

ND

ND

PAHs

Various

Various

Various

Various

ND

ND

ND

ND

ND

ND

ND

ND

Other VOCs

Various

Various

Various

Various

ND

ND

ND

ND

ND

ND

ND

ND

SVOCs

Various

Various

Various

Various

ND

ND

ND

ND

ND

ND

ND

ND

Notes:

(a)   Underlined and Bold Results = concentration exceeds the Dutch “B” values; Underlined, Bold, and Italic Results = concentration exceeds the Dutch “C” values;

(b)   N/A = not available; ND = not detectable.

(c)    Mineral oil is sum of total detected results of light diesel, heavy diesel and heavy oil.

(d)   Total xylene is sum of m,p-xylene and o-xylene.

(e)   Duplicate samples were analysed for this sampling location. Higher results were selected for presenting in the table where the two sample results differ from each other.

 

 


Table 5.1b  Analytical Results for Groundwater Samples (a) (b)

Parameter

Unit

Dutch

‘A’

Dutch

‘B’

Dutch

‘C’

Report

Limit

DH1

DH2

DH3

DH4

DH5

DH6 (f)

DH7

DH8

pH

 

 

 

 

0.1

7.2

6.4

7.9

7.4

7.6

7.6

7.4

7.7

TPH

 

 

 

 

 

 

 

 

 

 

 

 

 

Gasoline (C6-C9)

mg/L

10

40

150

20

ND

ND

ND

ND

ND

ND

ND

ND

Light Diesel (C10-C14)

mg/L

N/A

N/A

N/A

50

63

91

ND

ND

ND

ND

ND

ND

Heavy Diesel (C15-C28)

mg/L

N/A

N/A

N/A

100

1,460

2,590

1,590

712

1,400

733

1,560

125

Heavy Oil (C29-C36)

mg/L

N/A

N/A

N/A

50

ND

78

1,490

368

1,720

79

62

79

Mineral Oil (c)

mg/L

20

200

600

N/A

1,523

2,759

3,080

1,080

3,120

812

1,622

204

BTEX

 

 

 

 

 

 

 

 

 

 

 

 

 

Benzene

mg/L

0.2

1

5

5

ND

ND

ND

ND

ND

ND

ND

ND

Chlorobenzene

mg/L

0.02

0.5

2

5

ND

ND

ND

ND

ND

ND

ND

ND

Toluene

mg/L

0.5

15

50

5

ND

ND

ND

ND

ND

ND

ND

ND

Ethyl-benzene

mg/L

0.5

20

60

5

ND

ND

ND

ND

ND

ND

ND

ND

m,p-Xylene

mg/L

N/A

N/A

N/A

10

ND

ND

ND

ND

ND

ND

ND

ND

o-Xylene

mg/L

N/A

N/A

N/A

5

ND

ND

ND

ND

ND

ND

ND

ND

Total xylene (d)

mg/L

0.5

20

60

N/A

ND

ND

ND

ND

ND

ND

ND

ND

PAHs

mg/L

Various

Various

Various

Various

ND

ND

ND

ND

ND

ND

ND

ND

Other VOCs (e)

 

 

 

 

 

 

 

 

 

 

 

 

 

Chloroform

mg/L

N/A

N/A

N/A

5

ND

ND

8

ND

ND

ND

ND

ND

SVOCs (e)

 

 

 

 

 

 

 

 

 

 

 

 

 

Dimethyl phthalate

mg/L

-

2

ND

ND

ND

ND

ND

ND

ND

ND

Diethyl phthalate

mg/L

-

2

ND

ND

ND

ND

ND

ND

ND

ND

Di-n-butyl phthalate

mg/L

-

2

44

132

66

31

459

47

57

46

Butyl benzyl phthalate

mg/L

-

2

ND

ND

ND

ND

ND

ND

ND

ND

Bis(2-ethylhexyl) phthalate

mg/L

-

20

ND

ND

32

ND

21

ND

ND

ND

Di-n-octyl phthalate

mg/L

-

2

ND

ND

ND

ND

ND

ND

ND

ND

Phthalates (sum)

mg/L

5 (g)

-

44

132

98

31

480

47

57

46

Notes:

(a)    Underlined and Bold Results = concentration that exceed the Dutch “B” values; Underlined, Bold, and Italic Results = concentration that exceed the Dutch “C” values.

(b)    N/A = not available; ND = not detectable.

(c)    Mineral oil is sum of light diesel, heavy diesel and heavy oil.

(d)    Total xylene is sum of m,p-xylene and o-xylene.

(e)    Only the compounds in the group that were detected in at least one sample are shown.

(f)     Duplicate samples were analysed for this sampling location. Higher results were selected for presenting in the table where the two sample results differ from each other.

(g)    Dutch Intervention Value (DIV) of total phthalates was adopted to compare with the measured results.


5.2                            Results for Soil Samples

5.2.1                      Total Petroleum Hydrocarbons (TPH)

TPH in the fractions of light diesel, heavy diesel and heavy oil was detected in one soil sample collected from TP3 at a depth 0.9 m bgl.  The sum of light diesel, heavy diesel and heavy oil for this soil sample (1,858 mg/kg) exceeded the Dutch ‘B’ value for mineral oil (ie 1,000 mg/kg).

5.2.2                      BTEX

Benzene, toluene, ethylbenzene and xylene were not detected at concentrations exceeding the laboratory reporting limits in any soil sample collected from the Site.

5.2.3                      PAHs

No target PAHs were detected at concentrations exceeding the laboratory reporting limits in the soil samples collected from the Site.

5.2.4                      VOCs

No target VOCs were detected at concentrations exceeding the laboratory reporting limits in the soil samples collected from the Site.

5.2.5                      SVOCs

No target SVOCs were detected above the laboratory reporting limits in the soil samples collected from the Site.

5.3                            Results for Groundwater Samples

5.3.1                      Total Petroleum Hydrocarbons (TPH)

Light diesel, heavy diesel and/or heavy oil were detected in all groundwater samples collected from the Site.  With the exception of the groundwater sample from DH8, the sum of light diesel, heavy diesel and heavy oil fractions for the groundwater samples ranged from 812 mg/L to 3,120 mg/L and exceeded the Dutch ‘ C’ value (600 mg/L for mineral oil).  The sum of the light diesel, heavy diesel and heavy oil fractions for the groundwater sample collected from DH8 was 204 mg/L which is marginally above the ‘B’ value (ie 200 mg/L) for mineral oil.

5.3.2                      BTEX

Benzene, toluene, ethylbenzene and xylene were not detected at concentrations exceeding the laboratory reporting limits in any groundwater sample collected from the Site.

5.3.3                      PAHs

No target PAHs were detected at concentrations exceeding the laboratory reporting limits in the groundwater samples collected from the Site.

5.3.4                      VOCs

No VOCs were detected in the groundwater samples collected from the Site at concentrations exceeding either the laboratory reporting limits or the applicable EPD Dutch ‘B’ or ‘C’ values except chloroform at DH3.  8 mg/L of Chloroform was detected at DH3 which is above the reporting limit of 5 mg/L.

5.3.5                      SVOCs

Two SVOCs (di-n-butyl phthalate and bis (2-ethylhexyl) phthalate were detected in the groundwater samples collected.  Di-n-butyl phthalate were detected at concentrations ranging from 31 to 459 mg/L in the groundwater samples from all groundwater wells whereas bis (2-ethylhexyl) phthalate were detected at concentrations ranging from 21 to 32 mg/L in the groundwater samples from DH3 and DH5.  The sum of phthalates for the groundwater sample from all groundwater wells was higher than the DIV of 5 mg/L for total phthalates.

5.4                            QA /QC Sample Results and Data Usability

5.4.1                      Field QA/QC Sample Results

Assessment of field QA/QC sample results included checking of relative percent difference (RPD) for field duplicate samples, equipment blank and trip blank samples.

RPD Results

The relative percent difference (RPD[3]) was used to assess the sampling and laboratory reproducibility and precision.  The USEPA acceptable limits for RPD are less than 30% for groundwater and less than 50% for soil.  No RPD is required where the sample result is below two times the method detection limits or below the method detection limits.

The values of RPD calculated the detected results for the soil duplicate samples (TP2 0.8 and DH9 0.8) were within the 50% acceptance limit. 

The RPD values calculated for the groundwater duplicate samples (DH6 and DH9) were within the 30% acceptance limit.

Equipment and Trip Blank Sample Results

The results of the equipment or trip blank samples are summarized in Table 5.4a.

Table 5.4a      Summery of Detected QA/QC Sample Results

Sample ID

Sample

Detected parameter

Detected result

(µg/L)

Laboratory report limit (µg/L)

EQ BLK3

Equipment blank sample

TPH (C6 - C9 fraction)

22

20

EQ BLK3

Equipment blank sample

Toluene

22

5

EQ BLK3

Equipment blank sample

Phenol

8

2

Trip blank 4

Trip blank sample

Di-n-butyl phthalate

5

2

TPH (C6-C9 fraction), toluene, and phenol were detected in the equipment blank sample (EQ BLK3), but was not detected in the associated soil sample DH8 0.8m.  The equipment blank sample result, therefore, did not impact on the associated soil sample results.

Di-n-butyl phthalate was detected in Trip Blank 4 and in the associated groundwater samples (DH1 and DH2).  The detected concentrations of di-n-butyl phthalate in the associated groundwater samples DH1 and DH2 were 44 and 132 µg/L, respectively, which are more than 4 times higher than the concentration detected in the trip blank.  In accordance with the USEPA Region 1’s Data Validation Guidance, the detected di-n-butyl phthalate results in the trip blank did not impact the sample results.

5.4.2                      Laboratory Internal QA/QC Sample Results

The laboratory QA/QC sample results included surrogate recoveries, matrix spike sample, laboratory duplicate samples and method blanks and met their respective requirements.

5.5                            Data usability

Based on the review of QA/QC sample results, all laboratory results for the soil and groundwater samples are considered useable.

 

6                                  Contamination Assessment for Soil and Groundwater

6.1                            Soil

Elevated concentrations of light diesel, heavy diesel and heavy oil were detected in one soil sample collected from location (TP3) at a depth near the ground surface (ie 0.9 m bgl).  The detected TPH had the highest concentration (1,170 mg/kg) for heavy diesel.  The total concentration of light diesel, heavy diesel and heavy oil in this soil sample was 1,858 mg/kg and exceeded the Dutch ‘B’ value of 1,000 mg/kg.  No TPH was detected in any of other soil samples collected from the site.

6.2                            Groundwater

TPH including light diesel, heavy diesel, and heavy oil fractions was identified in the groundwater samples collected from the wells DH1 and DH2.  Heavy diesel and heavy oil were detected in the groundwater samples collected at the other six locations.  Of the TPH fractions, diesel oil was detected at the highest concentrations ranging from 100 to 2,590 mg/L.  The total concentrations of light diesel, heavy diesel and heavy oil for all groundwater samples taken from the site (ranged from 812 to 3,080 mg/L) exceeded the Dutch ‘C’ value for mineral oil (ie 600 mg/L) with the exception of the sample from DH8.  The total of light diesel, heavy diesel and heavy oil for DH8 (204 mg/L) marginally exceeded the Dutch ‘B’ value for mineral oil (200 mg/L).

Di-n-butyl phthalate was identified in the groundwater samples collected from all wells (DH1 to DH8) and bis (2-ethylhexyl) phthalate was detected in the groundwater samples from DH3 and DH5.   The sum of phthalates for the groundwater sample from all groundwater wells was higher than the DIV of 5 mg/L for total phthalates.  It should be noted that groundwater is not used for either domestic or industrial purposes at the site.

6.3                            Qualitative Risk Assessment

6.3.1                      Potential Source of TPH Contamination in Soil and TPH, Di-n-butyl Phthalate and Bis (2-ethylhexyl) Phthalate in Groundwater

The Castle Peak ‘A’ and ‘B’ Power Station (commenced operation between 1982 and 1985) has several oil storage tanks and associated pipe lines.

The Castle Peak “B” power station has been operating since 1985.  The power station was developed on a partially undeveloped land and partially reclaimed land. 

The fuel oil day tank, which is located up gradient of the location where soil TPH contamination was detected, is located above ground level and was commissioned at the same time as the power station.  The tank is surrounded by a concrete pavement and is provided with secondary containment.  No oil spills and leakages have been reported at the tank and none were observed during the site.  An oil pipe leakage near the fuel oil pump house was reported to the Marine Department and the EPD in July 2004.

6.3.2                      Chemicals of Concern

The chemicals of concern are mainly TPH in the soil and groundwater and di-n-butyl phthalate and bis (2-ethylhexyl) phthalate in groundwater.  The TPH included light diesel (C10-C14), heavy diesel (C15-C28) and heavy oil (C29-C36) fractions.

6.3.3                      Potential Migration and Exposure

The potential transport mechanism for the TPH contamination in surface soil at TP3 and TPH, di-n-butyl phthalate and bis (2-ethylhexyl) phthalate in the groundwater in the Site area is the flow of shallow groundwater underneath the site which was measured at about 1.3 to 2.5 mPD.  The groundwater flow within the Site area is likely influenced by tidal movements as the Site is located on a reclaimed area approximately 100 to 400 m from the waterfront.

As the Site area is paved, and groundwater is not used for either domestic or industrial purposes at the Site and in the adjacent areas, the potential exposure to TPH, di-n-butyl phthalate and bis (2-ethylhexyl) phthalate in groundwater could only take place during the demolition and construction stages of the Project.  The potential exposure pathways include dermal contact and accidental ingestion of the soil and groundwater.

6.3.4                      Potential Receptor

During the demolition of the facilities and the construction phases, potential on-site receptors include workers involved in demolition and construction actives who may be handling or come into contact with the contaminated materials.  Mitigations measures are proposed in the Remediation Action Plan (RAP) to minimise worker exposure during this period.  No adverse impacts are anticipated after the proposed measures have been implemented.

The site and the surrounding areas are used by Castle Peak ‘B’ power station.  The site area is fully paved and direct human contact with the underlying soil materials is not anticipated during current or future operations.  As the groundwater is not used at the area for either domestic or industrial purposes there is no on-site or off-site potential receptor of the TPH, di-n-butyl phthalate and bis (2-ethylhexyl) phthalate contaminated groundwater.

 

7                                  conclusions and Recommendations

A site investigation was completed and the findings are reported in this CAR.  The land contamination assessment was performed in accordance with the procedures and requirements set out in the CAP.  The CAP made reference to EPD’s Practice Note for Professional Persons (ProPECC PN 3/94) and Guidance Notes for Investigation and Remediation Contaminated Site of Petrol Filling Stations, Boatyard and Car Repair/Dismantling Workshops. 

The conclusions of the land contamination assessment are summarized below.

7.1                            Soil

TPH was detected at a concentration (1,858 mg/kg) which exceeded the EPD Dutch ‘B’ value for mineral oil (1,000 mg/kg) in a soil sample taken from one location (TP3), at a depth 0.9 m bgl. The detected TPH concentration was in the light diesel (83 mg/kg), heavy diesel (1,170 mg/kg) and heavy oil fractions (605 mg/kg).  Other than this, no TPH was detected in any soil sample.

7.2                            Groundwater

TPH in the fractions of heavy diesel and heavy oil were detected at concentrations which ranged from 204 to 3,120 µg/L, exceeding the Dutch ‘B’ value (200 µg/L for mineral oil) in all groundwater samples.  Seven out of the eight groundwater samples exceeded the Dutch ‘C’ value (600 µg/L for mineral oil).

As groundwater is not used for either domestic or industrial purposes at the site and in the adjacent areas, remediation of groundwater contamination of the Site is not considered necessary.  If groundwater is encountered during the construction of the Project, the groundwater abstracted or collected should be recharged back to the site.  Health and safety control measures will also be implemented for the workers who may come into contact with contaminated groundwater.

 



([1])  The soil drilling was carried out using rotary drilling rigs and soil sample collection was conducted using split-barrel samplers following the standard procedures described in the ASTM’s D1586-99 Standard Test Method for Penetration Test and Split-Barrel Sampling of Soils.

([2])  USEPA’s Groundwater Sampling Guidelines for Superfund and RCRA Project Managers, Attachment 4 - Standard Operating Procedure for the Standard/Well-Volume Method for Collecting a Groundwater Sample released in the USEPA Technology Innovation Program (TIP).   

[3] RPD is calculated from the detected results of field duplicate samples, which should be higher than two times the detection limits.