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  • 1.
    Khasevani, Sepideh G.
    et al.
    Luleå tekniska universitet, Institutionen för teknikvetenskap och matematik, Materialvetenskap.
    Nikjoo, Dariush
    Luleå tekniska universitet, Institutionen för teknikvetenskap och matematik, Materialvetenskap.
    Ojwang, Dickson O.
    Department of Chemistry – Ångström Laboratory, Uppsala University, Box 538, SE-751 21, Uppsala, Sweden.
    Nodari, Luca
    Dipartimento di Scienze Chimiche, Università degli Studi di Padova, 35131 Padova, Italy; Istituto di Chimica della Materia Condensata e di Tecnologie per l’Energia, ICMATE-CNR, 35127 Padova, Italy.
    Sarmad, Shokat
    Technical Chemistry, Department of Chemistry, Chemical-Biological Centre, Umeå University, SE-90871 Umeå, Sweden.
    Mikkola, Jyri-Pekka
    Technical Chemistry, Department of Chemistry, Chemical-Biological Centre, Umeå University, SE-90871 Umeå, Sweden; Industrial Chemistry & Reaction Engineering, John Gadolin Process Chemistry Centre, Åbo Akademi University, Biskopsgatan 8, Fl-20500 Åbo-Turku, Finland.
    Rigoni, Federica
    Department of Molecular Sciences and Nanosystems, Ca’ Foscari University of Venice, 30170 Venezia-Mestre, Italy.
    Concina, Isabella
    Luleå tekniska universitet, Institutionen för teknikvetenskap och matematik, Materialvetenskap.
    The beauty of being complex: Prussian blue analogues as selective catalysts and photocatalysts in the degradation of ciprofloxacin2022Inngår i: Journal of Catalysis, ISSN 0021-9517, E-ISSN 1090-2694, Vol. 410, s. 307-319Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We investigate the performance of four Prussian blue analogues (PBAs) as catalysts for the selective degradation of ciprofloxacin in water, under both dark and illumination conditions. We show that no light is actually needed to induce a selective degradation of the molecular target, while light irradiation spurs the process, without, however, resulting in the commonly reported photolysis-supported breaking down. We present a systematic characterization of the PBAs aiming at interpreting the catalytic outcomes in the light of a classic coordination chemistry analysis, empowered by the most recent findings in literature. We show that varying the transition metal binding the N atom of the cyanide bridge is key to promote photoinduced charge generation and transfer, which effectively disrupts the molecular target. The analysis of the materials before and after the irradiation with solar simulated light results in a change of the lattice parameters, indicating the possibility of a light-induced spin cross-over.

  • 2.
    Khasevani, Sepideh Gholizadeh
    et al.
    Luleå tekniska universitet, Institutionen för samhällsbyggnad och naturresurser, Geovetenskap och miljöteknik.
    Nikjoo, Dariush
    Luleå tekniska universitet, Institutionen för teknikvetenskap och matematik, Materialvetenskap.
    Chaxel, Cécile
    Luleå tekniska universitet, Institutionen för teknikvetenskap och matematik, Materialvetenskap.
    Umeki, Kentaro
    Luleå tekniska universitet, Institutionen för teknikvetenskap och matematik, Energivetenskap.
    Sarmad, Shokat
    Wallenberg Wood Science Center, Department of Chemistry Technical Chemistry, Department of Chemistry, Chemical-Biological Centre, Umeå University, SE-90871 Umeå, Sweden.
    Mikkola, Jyri-Pekka
    Wallenberg Wood Science Center, Department of Chemistry Technical Chemistry, Department of Chemistry, Chemical-Biological Centre, Umeå University, SE-90871 Umeå, Sweden; Industrial Chemistry & Reaction Engineering, Johan Gadolin Process Chemistry Centre, Åbo Akademi University, FI-20500 Åbo-Turku, Finland.
    Concina, Isabella
    Luleå tekniska universitet, Institutionen för teknikvetenskap och matematik, Materialvetenskap.
    Empowering Adsorption and Photocatalytic Degradation of Ciprofloxacin on BiOI Composites: A Material-by-Design Investigation2023Inngår i: ACS Omega, E-ISSN 2470-1343, Vol. 8, nr 46, s. 44044-44056Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Binary and ternary composites of BiOI with NH2-MIL-101(Fe) and a functionalized biochar were synthesized through an in situ approach, aimed at spurring the activity of the semiconductor as a photocatalyst for the removal of ciprofloxacin (CIP) from water. Experimental outcomes showed a drastic enhancement of the adsorption and the equilibrium (which increased from 39.31 mg g–1 of bare BiOI to 76.39 mg g–1 of the best ternary composite in 2 h time), while the kinetics of the process was not significantly changed. The photocatalytic performance was also significantly enhanced, and the complete removal of 10 ppm of CIP in 3 h reaction time was recorded under simulated solar light irradiation for the best catalyst of the investigated batch. Catalytic reactions supported by different materials obeyed different reaction orders, indicating the existence of different mechanisms. The use of scavengers for superoxide anion radicals, holes, and hydroxyl radicals showed that although all these species are involved in CIP photodegradation, the latter play the most crucial role, as also confirmed by carrying out the reaction at increasing pH conditions. A clear correlation between the reduction of BiOI crystallite sizes in the composites, as compared to the bare material, and the material performance as both adsorbers and photocatalyst was identified. 

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