Heavy metals such as zinc cannot be degraded by microorganisms and form long contaminant plumes in groundwater. Conventional methods for remediating heavy metal-contaminated sites are for example excavation and pump-and-treat, which is expensive and requires very long operation times. This induced interest in new technologies such as in situ adsorption barriers for immobilization of heavy metal contamination. In this study, we present steps and criteria from laboratory tests to field studies, which are necessary for a successful implementation of an in situ adsorption barrier for immobilizing zinc. Groundwater and sediment samples from a contaminated site were brought to the lab, where the adsorption of zinc to Goethite nanoparticles was studied in batch and in flow-through systems mimicking field conditions. The Goethite nanoparticles revealed an in situ adsorption capacity of approximately 23 mg Zn per g Goethite. Transport experiments in sediment columns indicated an expected radius of influence of at least 2.8 m for the injection of Goethite nanoparticles. These findings were validated in a pilot-scale field study, where an in situ adsorption barrier of ca. 11 m × 6 m × 4 m was implemented in a zinc-contaminated aquifer. The injected nanoparticles were irreversibly deposited at the desired location within <24 h, and were not dislocated with the groundwater flow. Despite a constantly increasing inflow of zinc to the barrier and the short contact time between Goethite and zinc in the barrier, the dissolved zinc was effectively immobilized for ca. 90 days. Then, the zinc concentrations increased slowly downstream of the barrier, but the barrier still retained most of the zinc from the inflowing groundwater. The study demonstrated the applicability of Goethite nanoparticles to immobilize heavy metals in situ and highlights the criteria for upscaling laboratory-based determinants to field-scale.
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http://dx.doi.org/10.1016/j.scitotenv.2021.151066 | DOI Listing |
Materials (Basel)
December 2024
Department of Chemistry, Morgan State University, 1700 East Cold Spring Lane, Baltimore, MD 21251, USA.
Metal-organic frameworks (MOFs) are hybrid inorganic-organic 3D coordination polymers with metal sites and organic linkers, which are a "hot" topic in the research of sorption, separations, catalysis, sensing, and environmental remediation. In this study, we explore the molecular mechanism and kinetics of interaction of the new copper porphyrin aluminum metal-organic framework (actAl-MOF-TCPPCu) compound with a vapor of the volatile organic sulfur compound (VOSC) diethyl sulfide (DES). First, compound was synthesized by post-synthetic modification (PSM) of Al-MOF-TCPPH compound by inserting Cu ions into the porphyrin ring and characterized by complementary qualitative and quantitative chemical, structural, and spectroscopic analysis.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China. Electronic address:
Developing efficient and cost-effective rare earth element-based electrocatalysts for water splitting remains a significant challenge. To address this, interface engineering and charge modulation strategies were employed to create a three-dimensional coral-like CeF/MoO heterostructure electrocatalyst, grown in situ on the multistage porous channels of carbonized sugarcane fiber (CSF). Integrating abundant CeF/MoO heterostructure interfaces and numerous oxygen vacancy defects significantly enhanced the catalyst's active sites and molecular activation capabilities.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
School of Environment, Tsinghua University, Beijing 100084, China. Electronic address:
Using sewage sludge compost (SSC) for abandoned mine land reclamation supports ecological sustainability, but the environmental behavior of heavy metals in this process lacks systematic field validation. Here we analyzed the dynamic changes in heavy metal composition in topsoil, surface runoff, and subsurface infiltration after large-scale reclamation. Results show that SSC application promoted plant growth by 2-4 times, enhanced the physicochemical structure of the topsoil, and increased the levels of organic matter and inorganic nutrients.
View Article and Find Full Text PDFCatal Sci Technol
December 2024
Laboratory of Inorganic Materials and Catalysis, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology Eindhoven The Netherlands
In this work, we study the reducibility of a PdO precursor placed by strong electrostatic adsorption on either NiO or SiO of NiO/SiO obtained by incipient wetness impregnation. The catalysts were characterized by HAADF-STEM, quasi- XPS, CO IR spectroscopy and H chemisorption as a function of the reduction temperature and evaluated for their performance in cinnamaldehyde hydrogenation. PdO on SiO requires reduction at higher temperatures to achieve appreciable rates of cinnamaldehyde hydrogenation.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Research Institute of Industrial Catalysis, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, PR China.
The main bottleneck in the catalytic combustion of chlorinated volatile organic compounds (CVOCs) is deactivation and the production of chlorine-containing byproducts originating from the chlorine species deposited on the catalyst. Herein, Ru supported on SnO (Ru/SnO) was prepared with the lattice matching principle. As RuO and SnO are both rutile phases, Ru species were present as highly dispersed RuO particles on the Ru/SnO catalyst.
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