Effluent treatment from flexographic printing was investigated by precipitation/coagulation and electrochemical oxidation over boron-doped diamond electrodes. Precipitation with 3 g/L of lime led to complete removal of effluent turbidity (initial value of about 410 NTU) but only about 20% chemical oxygen demand (COD) decrease (initial value of about 1,900 mg/L). Higher lime dosages (up to 15 g/L) had no effect on separation. On the other hand, coagulation with alum in the range 0.05-1 mM failed to enhance the extent of solids separation achieved by gravity settling alone (i.e. about 60%). Preliminary electrochemical oxidation experiments in the presence of sulphuric acid as supporting electrolyte showed that treatment performance (in terms of COD removal and decrease in sample absorbance at 300 nm) increased with increasing applied current. The latter was more efficiently utilized at shorter treatment times and lower currents with efficiency reaching 30%. Following lime precipitation, the effluent was electrochemically oxidized at alkaline conditions for 360 min yielding 64% absorbance reduction and 50% COD removal (this corresponds to 60% overall COD removal for the combined process). The rather low electrochemical treatment performance may be attributed to limestone deposition and fouling of electrodes and other electrochemical reactor components as evidenced by the gradual drop in conductivity/current throughout the operation.
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http://dx.doi.org/10.2166/wst.2009.682 | DOI Listing |
J Am Chem Soc
January 2025
Helmholtz-Institute Erlangen-Nürnberg for Renewable Energy (IET-2), Forschungszentrum Jülich, 91058 Erlangen, Germany.
Recently, cobalt-based oxides have received considerable attention as an alternative to expensive and scarce iridium for catalyzing the oxygen evolution reaction (OER) under acidic conditions. Although the reported materials demonstrate promising durability, they are not entirely intact, calling for fundamental research efforts to understand the processes governing the degradation of such catalysts. To this end, this work studies the dissolution mechanism of a model CoO porous catalyst under different electrochemical conditions using online inductively coupled plasma mass spectrometry (online ICP-MS), identical location scanning transmission electron microscopy (IL-STEM), and differential electrochemical mass spectrometry (DEMS).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
University of Oxford, Chemistry, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
The catalytic action of enzymes of a cascade trapped within a mesoporous electrode material is simultaneously energized, controlled and observed through the efficient, reversible electrochemical NAD(P)(H) recycling catalyzed by one of the enzymes. In their nanoconfined state, nicotinamide cofactors are tightly channeled current carriers, mediating multi-step reactions in either direction (oxidation or reduction) with a rapid response time. By incorporating a hydrogen‑borrowing enzyme pair, the internal action of which opposes the external voltage bias driving oxidation or reduction, a reduction process can be performed under overall oxidizing conditions, and vice versa.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
Department of Physical Sciences, Chemistry Division, College of Science, Jazan University, P.O. Box. 114, Jazan 45142, Kingdom of Saudi Arabia.
Herein, electrochemical sensing of paracetamol in polluted water was achieved using facile-synthesized tungsten oxide nanoparticles. Ion exchange resin has been used as a sustainable preparation route, while the prepared nanoparticles have been characterized by XRD and SEM analyses. Orthorhombic WO·HO nano-plates have been synthesized a facile preparation method, where the crystal size has been calculated as 25-33 nm, and these results were used to create a 3D model of the prepared WO·HO nano-plates.
View Article and Find Full Text PDFNat Commun
January 2025
State Key Laboratory of Organometallic Chemistry, Shanghai of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, PR China.
Motivated by the inherent benefits of synergistically combining electrochemical methodologies with nickel catalysis, we present here a Ni-catalyzed enantioselective electroreductive cross-coupling of benzyl chlorides with aryl halides, yielding chiral 1,1-diaryl compounds with good to excellent enantioselectivity. This catalytic reaction can not only be applied to aryl chlorides/bromides, which are challenging to access by other means, but also to benzyl chlorides containing silicon groups. Additionally, the absence of a sacrificial anode lays a foundation for scalability.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Shenzhen University, College of Chemistry and Environmental Engineering, CHINA.
Rationally manipulating the in-situ formed catalytically active surface of catalysts remains a significant challenge for achieving highly efficient water electrolysis. Herein, we present a bias-induced activation strategy to modulate in-situ Ga leaching and trigger the dynamic surface restructuring of lamellar Ir@Ga2O3 for the electrochemical oxygen evolution reaction. The in-situ reconstructed Ga-O-Ir interface sustains high water oxidation rates at OER overpotentials.
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