Oxidative Mineralization and Dechlorination Effects of Micron/Nanosize Birnessite on Pentachlorophenol in Contaminated Soil

Chlorinated aromatic organic compounds are extremely toxic to the environment and cause cancer to the human body. Pentachlorophenol (PCP) is a hydrophobic and ionic organic compound that is employed as a production material in various industries. Although the Taiwanese government has banned the use...

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Veröffentlicht in:Water, air, and soil pollution air, and soil pollution, 2019-05, Vol.230 (5), p.1-11, Article 97
Hauptverfasser: Chien, Shui-Wen Chang, Chou, Jen-Shen, Chen, Shyh-Wei, Chang, Jih-Hsing, Chen, Shou-Hung
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container_title Water, air, and soil pollution
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creator Chien, Shui-Wen Chang
Chou, Jen-Shen
Chen, Shyh-Wei
Chang, Jih-Hsing
Chen, Shou-Hung
description Chlorinated aromatic organic compounds are extremely toxic to the environment and cause cancer to the human body. Pentachlorophenol (PCP) is a hydrophobic and ionic organic compound that is employed as a production material in various industries. Although the Taiwanese government has banned the use of PCP for years, large PCP-contaminated areas remain in Southern Taiwan. Chemical oxidation, which has been proposed as a viable method for restoring PCP-contaminated areas, involves the use of micronanosize birnessite (δ-MnO 2 ), which is a type of manganese oxide and a natural mineral in soil environments. The goal of this study was to simulate the decontamination of the underlying soil of the PCP-contaminated areas, which is situated in anaerobic and lightless environment. Through the use of a self-developed gas release and absorption reaction flask, the oxidative mineral decarboxylation and dechlorination effects of δ-MnO 2 on PCP in aerobic and anaerobic (with oxygen removed through the use of nitrogen) environments without light were investigated. Results indicated that adding δ-MnO 2 facilitated the oxidative decarboxylation and dechlorination of PCP and the release of Cl − in an aerobic, lightless environment without microbial activity. In the anaerobic environment, the oxidative decarboxylation effect of δ-MnO 2 on PCP decreased significantly, and the dechlorination effect was the primary reaction. Accordingly, adding δ-MnO 2 inorganically destroys aromatic benzene and releases CO 2 and Cl − . The molar ratio between CO 2 and Cl − was calculated to assess the mechanisms of the distinct reaction systems. The parameters and data acquired from the experiment, which involved simulating the conditions of the contaminated areas, can be used in planning the on-site management of the PCP contamination; in particular, these parameters and data provide a reference for eliminating PCP from underlying soil—including groundwater-saturated layers.
doi_str_mv 10.1007/s11270-019-4151-8
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Pentachlorophenol (PCP) is a hydrophobic and ionic organic compound that is employed as a production material in various industries. Although the Taiwanese government has banned the use of PCP for years, large PCP-contaminated areas remain in Southern Taiwan. Chemical oxidation, which has been proposed as a viable method for restoring PCP-contaminated areas, involves the use of micronanosize birnessite (δ-MnO 2 ), which is a type of manganese oxide and a natural mineral in soil environments. The goal of this study was to simulate the decontamination of the underlying soil of the PCP-contaminated areas, which is situated in anaerobic and lightless environment. Through the use of a self-developed gas release and absorption reaction flask, the oxidative mineral decarboxylation and dechlorination effects of δ-MnO 2 on PCP in aerobic and anaerobic (with oxygen removed through the use of nitrogen) environments without light were investigated. Results indicated that adding δ-MnO 2 facilitated the oxidative decarboxylation and dechlorination of PCP and the release of Cl − in an aerobic, lightless environment without microbial activity. In the anaerobic environment, the oxidative decarboxylation effect of δ-MnO 2 on PCP decreased significantly, and the dechlorination effect was the primary reaction. Accordingly, adding δ-MnO 2 inorganically destroys aromatic benzene and releases CO 2 and Cl − . The molar ratio between CO 2 and Cl − was calculated to assess the mechanisms of the distinct reaction systems. 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Pentachlorophenol (PCP) is a hydrophobic and ionic organic compound that is employed as a production material in various industries. Although the Taiwanese government has banned the use of PCP for years, large PCP-contaminated areas remain in Southern Taiwan. Chemical oxidation, which has been proposed as a viable method for restoring PCP-contaminated areas, involves the use of micronanosize birnessite (δ-MnO 2 ), which is a type of manganese oxide and a natural mineral in soil environments. The goal of this study was to simulate the decontamination of the underlying soil of the PCP-contaminated areas, which is situated in anaerobic and lightless environment. Through the use of a self-developed gas release and absorption reaction flask, the oxidative mineral decarboxylation and dechlorination effects of δ-MnO 2 on PCP in aerobic and anaerobic (with oxygen removed through the use of nitrogen) environments without light were investigated. 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Pentachlorophenol (PCP) is a hydrophobic and ionic organic compound that is employed as a production material in various industries. Although the Taiwanese government has banned the use of PCP for years, large PCP-contaminated areas remain in Southern Taiwan. Chemical oxidation, which has been proposed as a viable method for restoring PCP-contaminated areas, involves the use of micronanosize birnessite (δ-MnO 2 ), which is a type of manganese oxide and a natural mineral in soil environments. The goal of this study was to simulate the decontamination of the underlying soil of the PCP-contaminated areas, which is situated in anaerobic and lightless environment. Through the use of a self-developed gas release and absorption reaction flask, the oxidative mineral decarboxylation and dechlorination effects of δ-MnO 2 on PCP in aerobic and anaerobic (with oxygen removed through the use of nitrogen) environments without light were investigated. Results indicated that adding δ-MnO 2 facilitated the oxidative decarboxylation and dechlorination of PCP and the release of Cl − in an aerobic, lightless environment without microbial activity. In the anaerobic environment, the oxidative decarboxylation effect of δ-MnO 2 on PCP decreased significantly, and the dechlorination effect was the primary reaction. Accordingly, adding δ-MnO 2 inorganically destroys aromatic benzene and releases CO 2 and Cl − . The molar ratio between CO 2 and Cl − was calculated to assess the mechanisms of the distinct reaction systems. The parameters and data acquired from the experiment, which involved simulating the conditions of the contaminated areas, can be used in planning the on-site management of the PCP contamination; in particular, these parameters and data provide a reference for eliminating PCP from underlying soil—including groundwater-saturated layers.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/s11270-019-4151-8</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7201-4936</orcidid></addata></record>
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subjects Anaerobic microorganisms
Analysis
Aromatic compounds
Atmospheric Protection/Air Quality Control/Air Pollution
Benzene
Biological activity
Birnessite
Cancer
Carbon dioxide
Chemical plants
Chlorinated solvents
Climate Change/Climate Change Impacts
Data acquisition
Decarboxylation
Dechlorination
Decontamination
Earth and Environmental Science
Environment
Environmental monitoring
Groundwater
Health aspects
Hydrogeology
Hydrophobicity
Industry
Manganese
Manganese compounds
Manganese dioxide
Manganese oxides
Microbial activity
Microorganisms
Mineralization
Organic chemistry
Organic compounds
Organic soils
Oxidation
Oxidation-reduction reactions
Parameters
Pentachlorophenol
Quartz
Soil
Soil contamination
Soil environment
Soil layers
Soil pollution
Soil Science & Conservation
Water Quality/Water Pollution
title Oxidative Mineralization and Dechlorination Effects of Micron/Nanosize Birnessite on Pentachlorophenol in Contaminated Soil
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