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WSP Sweden
1 
Figure 1.  Site Location along the Nissan River 
Figure 2: Site Layout 
 
Treatment of Chlorinated Solvents using 3‐D Microemulsion (3DMe®) 
allows for Housing Redevelopment in Sweden 
 
Remediation works were required at the Söderkaj site, in 
order  to  allow  the  completion  of  a  large  housing 
development  project  comprising  the  construction  of  330 
apartments  in  an  attractive  area  along  the  shore  of  the 
river  Nissan  in  Halmstad,  Sweden.  Historical  activities  at 
the site, including fisheries, metal plating, dry cleaning and 
maritime  industries,  have  led  to  chlorinated  solvent 
contamination  in  groundwater  and  PAH  and  metal 
contamination  in  the  shallow  soils.  The  hydrogeological 
conditions  for  the  area  are  controlled  by  seasonal 
variations  dependant  on  precipitation  and  sea  levels. 
Monitoring  and  infiltration  tests  have  shown  that  the 
groundwater level in the area is approximately 1‐2mBGL 
and  the  soil  profile  is  known  to  be  highly  variable  to  a 
depth of 7‐9mBGL. 
Shallow soils contaminated with PAH and metals were excavated and removed. Membrane interface probe 
(MIP) data was used to delineate both the vertical and lateral extent of the chlorinated solvent contamination 
at  the  site.  Groundwater  contamination  was 
determined to exist between 3 to 6mBGL.  
GROUNDWATER REMEDIAL STRATEGY 
3‐D  Microemulsion  (3DMe®),  supplied  by  Regenesis 
Ltd,  uses  a  3‐stage  donor  release  profile  allowing  for 
the  immediate,  mid‐range  and  long‐term  release  of 
hydrogen into the groundwater. The hydrogen is used 
to  increase  the  mass  and  activity  of  the  indigenous 
microorganisms  performing  reductive  dechlorination. 
3DMe is mixed with water to form a microemulsion for 
injection. Details of the injection are given in Table 1. 
The  remedial  objective  was  to  reduce  concentrations 
of  chlorinated  solvent  contamination  in  the 
groundwater  to  below  the  site  specific  target  level 
(SSTL) of 100μg/L in order to ensure the minimisation 
of the potential risk posed to human health. 
• DCE  Maximum  Concentration  –  19,000µg/L  at 
MIP8 (June 2007) 
• VC  Maximum  Concentration  –  12,000µg/L  at 
GV208 (March 2008) 
INTRODUCTION 
 
 
WSP Sweden
2 
3DMe application was undertaken in two stages to allow for demolition works onsite. Phase one, undertaken 
in June 2008, included the injection of 3DMe into the eastern and western portions of the plume. Phase two, 
undertaken in June 2009, included the injection of 3DMe in the previously inaccessible central plume area. The 
use of the high volume and self‐distributing properties of 3DMe allowed the number of injection points to be 
minimized, ensuring low application costs.  
Table 1. 3DMe Plume Treatment Summary 
Design Feature  Treatment # 1 
June 2008 
Treatment # 2 June 2009 
Area 1 ‐ Specification Area 2 ‐ Specification  Area 3 ‐ Specification
Saturated  thickness 
requiring treatment 
3m  3.5m  3.5m  2m  
Treatment area  380m2
  300m2
60m2
196m2
 
# of Injection points  32 points  23 points 6 points 14 points 
Injection spacing  4m by 4m
3DMe  dose  rate  in 
kgs/m of injection 
100L of 3DMe 
microemulsion /m 
108L of 3DMe 
microemulsion /m 
85L of 3DMe 
microemulsion /m 
1112L of 3DMe 
microemulsion /m 
3DMe material cost  < €20,000 
Total Project Costs  Investigations , risk assessments, evaluations & design of remediation ≈ €120,000 – €140,000 
Remediation Fieldwork (combined injections and material cost) ≈ €90,000  
Monitoring program ≈ €100,000
RESULTS 
Chlorinated solvent treatment was very successful, achieving a 98 – 99% reduction in concentrations within 18 
months  across  all  treatment  locations  (Figures  3‐8).  The  success  of  the  project  was  both  supported  and 
validated by the use of MIP data to get vertical plume delineation.  
 
 
 
Figure 3‐8 :  Contamination  levels from June 2007 – February 2010 
 
 
WSP Sweden
3 
 
Figure 9: Bacterial Counts Pre‐ & Post‐Treatment 
 
 
The degree of dechlorination was calculated to determine the progress of the reductive dechlorination on site. 
During the course of the works, full reductive dechlorination was observed as concentrations of DCE and VC 
were broken down to ethene.  
Geochemical  indicators  suggested  that  conditions  for  reductive  dechlorination  were  established  soon  after 
each of the application events.  Competing electron acceptors (e.g. oxygen, nitrate, sulphate etc), present in 
the  treatment  area  prior  to  the  injection  works,  were  rapidly  reduced  and  total  organic  compounds  (TOC) 
increased. 
Quantification of microbial populations pre‐ and 
post‐phase  one  treatment  works,  clearly 
demonstrated that the microbial populations had 
increased (Figure 9) and were supported by the 
controlled supply of hydrogen from 3DMe to the 
treatment  area.  This  was  complimented  by  a 
corresponding  increase  in  the  degradation  rate 
after the treatment was undertaken. 
Compound  Specific  Isotope  Analysis  (CSIA)  was 
undertaken  as  a  final  line  of  evidence.  
Transformation  of  organic  compounds  by 
biological processes can cause significant shifts in 
the ratios of 13
C to 12
C (δ13
C) in both the reactants and products of the reaction. This occurs as a result of the 
stronger molecular bonds formed by the heavier isotope 13
C in comparison to the 12
C. As a result, molecules 
with the lighter isotopes tend to be transformed more quickly, resulting in isotopic fractionation between the 
13
C  in  the  residual  reactant  and  of  the  12
C  in  the  initial  product.  For  example,  isotopic  fractionation  was 
reported for both DCE (‐9.1 to +5.2‰) and VC (‐22.0 to +27‰ ) at location GV208 between May 2008 and 
February 2010. This is evidence that the reduction in chlorinated solvent concentrations was not the result of 
abiotic processes such as physical dilution and dispersion, as isotope fractionation typically only occurs due to 
biological degradation of the chlorinated solvents.  
 
 
WSP Sweden
4 
 
CONCLUSION 
3DMe was applied to the groundwater in order to enhance the biodegradation of the chlorinated solvents 
onsite and allow redevelopment of the site. 
• Within two months of the 3DMe application, enhanced reductive dechlorination was observed 
• This was evidenced by; 
o Sequential production and degradation of daughter compounds 
o The geochemistry of the aquifer showing conditions ideal for reductive dehalogenation 
o An increase in biomass and activity of a reductive dechlorinator microbial consortia 
o Isotopic  fractionation  between  the  parent  and  daughter  compounds  resulting  from 
degradation 
o An overall reduction in chlorinated compound concentrations in the groundwater 
Contaminant levels throughout the plume were reduced to below the SSTLs within 18 months of the 3DMe 
application and regulatory acceptance for redevelopment of the site was secured. 
 
 
Regenesis  Ltd
Gareth Leonard 
District Manager, UK and Scandinavia 
+44 (0) 1833 630411 
gleonard@regenesis.com 
www.regenesis.com
WSP Environmental 
Lars Davidsson 
Principal Consultant 
+46 (0)35 18 11 00 
lars.davidsson@WSPGroup.se 
 www.wspenvironmental.com 
WSP Sweden

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