Microbiological cleanup is a widely used in situ remediation strategy for organic soil and groundwater contaminations. However, often the availability of electron acceptors and nutrients are limiting factors for microbial pollutant degradation in the field. Electromigration represents a new approach for the transport of microbiological agents in soil. In this study, the electrokinetic transport of the microbial electron acceptors nitrate and sulfate and of the nutrients ammonium and phosphate was compared. All experiments were performed under standardized conditions, i.e. with constant voltage in demineralized water and a model sandy soil. Average transport rates for nitrate, sulfate, poly-phosphate, and ammonium were 1.34 cm/h, 1.91 cm/h, 0.48 cm/h, and 0.40 cm/h, respectively, in single compound studies. Transport velocities were dependent on applied voltage gradient but not on the initial ion concentration. Additionally, electrokinetic transport was studied with ion mixtures. The ion distribution in the soil was significantly influenced by the pH profile and the associated voltage gradient.
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http://dx.doi.org/10.1080/10934520801974434 | DOI Listing |
Inorg Chem
January 2025
Faculty of Chemistry and Chemical Technology, University of Ljubljana, Večna pot 113, 1000 Ljubljana, Slovenia.
Hydrogen-bonded cocrystals have attracted considerable attention as they allow fine-tuning of properties through the choice of hydrogen-bond donors and acceptors. In this study, triphenylarsine oxide (PhAsO) is introduced as a strong hydrogen-bond acceptor molecule. Due to its higher Lewis basicity compared to triphenylphosphine oxide (PhPO), it acts as a strong hydrogen-bond acceptor, which is demonstrated in six new cocrystals with HO and -di(hydroperoxy)cycloalkanes.
View Article and Find Full Text PDFJ Org Chem
January 2025
Institute of Theoretical Chemistry and College of Chemistry, Jilin University, Changchun 130023, P.R. China.
Thiophene and pyrrole units are extensively utilized in light-responsive materials and have significantly advanced the field of organic photovoltaics (OPV). This progress has inspired our exploration of photosensitizers (PS) for photodynamic therapy (PDT). Currently, traditional PS face limitations in clinical application, including a restricted variety and narrow applicability.
View Article and Find Full Text PDFJ Phys Chem A
January 2025
College of Physics, Liaoning University, Shenyang 110036, China.
Based on the DCV-C system of fullerene acceptor organic solar cell active materials, the charge transfer process of D-A type molecular materials under the action of an external electric field () was explored. Within the range of electric field application, the excited state characteristics exhibit certain regular changes. Based on reducing the excitation energy, the excitation mode shows a trend of developing toward low excited states.
View Article and Find Full Text PDFChemistry
January 2025
The Hong Kong Polytechnic University, Department of Applied Biology and Chemical Technology, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Hom, Hong Kong (P.R. China), 000000, Hong Kong, HONG KONG.
A series of new (donor)₂-donor-π-acceptor (D2-D-π-A) and (acceptor)₂-donor-π-acceptor (A2-D-π-A) organic photosensitizers based on the framework of (Z)-2-cyano-3-(5-(4-(diphenylamino)phenyl)thiophen-2-yl)acrylic acid have been synthesized and characterized. By incorporating groups with different electron-donating or withdrawing abilities, such as dibenzothiophene (DBT), dibenzofuran (DBF), and triazine (TA), into the triphenylamine segment, their photophysical properties have been regulated. Theoretical calculations were used to explore how various donor-acceptor combinations influence their hydrogen production performance.
View Article and Find Full Text PDFDalton Trans
January 2025
Organometallics and Materials Chemistry Lab, Department of Chemistry, Indian Institute of Technology Hyderabad, Kandi, Sangareddy, Telangana, 502285, India.
The assessment of copper(I) and hydrogen interactions is challenging and should be approached with caution. In this paper, we report an assessment of multiple copper(I) and hydrogen interactions in two unique copper(I) thione cages. Copper(I) -heterocyclic thione cages [{Cu(-Br)(-L1)}] (1) and [{Cu(-I)(-L1)}] (2) were synthesized and characterized with proximity enforced Cu⋯H interactions.
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