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Removal of PCE/TCE from groundwater by peroxydisulfate activated with citric acid chelated ferrous iron at 13 °C

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22320%2F20%3A43920261" target="_blank" >RIV/60461373:22320/20:43920261 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S2352186420307665" target="_blank" >https://www.sciencedirect.com/science/article/pii/S2352186420307665</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.eti.2020.101004" target="_blank" >10.1016/j.eti.2020.101004</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Removal of PCE/TCE from groundwater by peroxydisulfate activated with citric acid chelated ferrous iron at 13 °C

  • Original language description

    Chlorinated organic compounds (CVOCs), such as tetrachloroethene (PCE) and trichloroethene (TCE) belong to the most abundant groundwater contaminants across the world. Over the last 15 years, in situ chemical oxidation (ISCO) using peroxydisulfate (PDS) activated by citric acid chelated ferrous ion (Fe(II)-CA) has been proposed as a suitable method for CVOCs removal from groundwater. However, published studies examining Fe(II)-CA activated PDS systems under laboratory conditions (T 20 °C) and in demineralized water have not provided a picture of the desired behavior of Fe(II)-CA activated PDS systems for CVOCs degradation at a lower temperature (T 13 °C) that are typical for shallow groundwater of larger areas of Europe and North America and in the presence of typical groundwater constituents, such as chlorides and bicarbonates. To resolve this knowledge gap, a series of batch experiments were conducted to investigate PCE, TCE and combined PCE/TCE degradation performance in Fe(II)-CA (fixed molar ratio Fe(II)/CA 2/3) activated and unactivated PDS systems based on their PDS/Fe(II) initial molar ratios (1/2.5; 1/1; 2.5/1; 5/1; 7.5/1; 10/1; 15/10). The experiments were conducted in artificially prepared groundwater (0.5 mmolL−1 CaCl2 HO, 0.5 mmolL−1 MgCl2 HO, 0.5 mmolL−1 NaHCO and 0.5 mmolL−1 KHCO3) at 13 °C. The results indicated that the most efficient PDS/Fe(II) initial molar ratios in terms of CVOCs removal efficiency and reaction stoichiometry efficiency (RSE) were 10/1 for PCE, and 15/1 for both TCE and combined PCE/TCE. Surprisingly, the efficiency of unactivated PDS systems was comparable to Fe(II)-CA activated PDS systems. The results therefore suggest that unactivated PDS could be an appropriate option for field applications and should not be disregarded within feasibility studies at given thermal and hydro-chemical conditions. Overall, conclusions made in this study deepened the knowledge of ISCO using PDS at lower than laboratory temperatures and in the presence of typical groundwater constituents, therefore, could be exploited by remediation practitioners as well as in future research work.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    20701 - Environmental and geological engineering, geotechnics

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Environmental Technology &amp; Innovation

  • ISSN

    2352-1864

  • e-ISSN

  • Volume of the periodical

    19

  • Issue of the periodical within the volume

    August 2020

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    101004

  • UT code for WoS article

    000580866600103

  • EID of the result in the Scopus database