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- ItemPreliminary Study on the Application of Temperature Swing Adsorption in Aqueous Phase for Pesticide Removal(London [u.a.] : Institute of Physics, 2018) Aumeier, B.; Dang, H.Q.A.; Wessling, M.Temperature swing adsorption (TSA) is a well-established process for gas purification. In this work, the feasibility of TSA in aqueous phase was studied. This concept could enable in situ adsorbent regeneration and thus fostering sustainable decentralized adsorption processes applied to water treatment. The adsorption processes with the use of granular activated carbon (GAC) have been widely applied to remove the residual amounts of pesticides in water treatment. Amitrole was chosen as a typical pesticide in this study, GAC was selected as the main adsorbent for amitrole removal. Adsorption isotherm experiments were conducted at different temperatures of 20°C, 57°C and 94°C to identify the most appropriate sorptive – sorbent system for dynamic adsorption and TSA research. Once the isotherm experiments were accomplished, breakthrough curve experiments were subsequently investigated. Finally, TSA process was conducted with the activated carbon regeneration at the elevated temperature of 125°C. Consequently, initial obtained results proved the feasibility of the proposed TSA technique for pesticide removal in aqueous phase.
- ItemHow activated carbon improves the performance of non-thermal plasma removing methyl ethyl ketone from a gas stream([Amsterdam] : Elsevier B.V., 2021) Schmidt, Michael; Kettlitz, Manfred; Kolb, Juergen F.The combination of non-thermal plasma (NTP), operated at room temperature and at atmospheric pressure in air and in combination with activated carbon filters offers a more efficient removal of VOCs from gas streams than each individual method alone. Efficiencies, synergies and mechanisms of this combination were investigated by means of comprehensive quantitative Fourier transform infrared spectroscopy analysis. Therefore, dry and wet synthetic air containing about 90 ppm of methyl ethyl ketone (MEK) were treated with non-thermal plasma (NTP) and an intentionally undersized activated carbon (AC) filter, separately and in combination. As a result, removal of about 50 % was achieved for NTP or AC alone but a removal close to 95 % was found for the combination. Ozone, generated by the NTP, was reduced by 55 % with the AC-filter. For the operation of the NTP with humid air, a decomposition of the pollutant on AC was observed even after the plasma was switched off.
- ItemControlling the speciation and reactivity of carbon-supported gold nanostructures for catalysed acetylene hydrochlorination(Cambridge : RSC, 2018) Kaiser, Selina K.; Lin, Ronghe; Mitchell, Sharon; Fako, Edvin; Krumeich, Frank; Hauert, Roland; Safonova, Olga V.; Kondratenko, Vita A.; Kondratenko, Evgenii V.; Collins, Sean M.; Midgley, Paul A.; López, Núria; Pérez-Ramírez, JavierCarbon-supported gold catalysts have the potential to replace the toxic mercuric chloride-based system applied industrially for acetylene hydrochlorination, a key technology for the manufacture of polyvinyl chloride. However, the design of an optimal catalyst is essentially hindered by the difficulties in assessing the nature of the active site. Herein, we present a platform of carbon supported gold nanostructures at a fixed metal loading, ranging from single atoms of tunable oxidation state and coordination to metallic nanoparticles, by varying the structure of functionalised carbons and use of thermal activation. While on activated carbon particle aggregation occurs progressively above 473 K, on nitrogen-doped carbon gold single atoms exhibit outstanding stability up to temperatures of 1073 K and under reaction conditions. By combining steady-state experiments, density functional theory, and transient mechanistic studies, we assess the relation between the metal speciation, electronic properties, and catalytic activity. The results indicate that the activity of gold-based catalysts correlates with the population of Au(i)Cl single atoms and the reaction follows a Langmuir-Hinshelwood mechanism. Strong interaction with HCl and thermodynamically favoured acetylene activation were identified as the key features of the Au(i)Cl sites that endow their superior catalytic performance in comparison to N-stabilised Au(iii) counterparts and gold nanoparticles. Finally, we show that the carrier (activated carbon versus nitrogen-doped carbon) does not affect the catalytic response, but determines the deactivation mechanism (gold particle aggregation and pore blockage, respectively), which opens up different options for the development of stable, high-performance hydrochlorination catalysts. © 2019 The Royal Society of Chemistry.
- ItemTin/vanadium redox electrolyte for battery-like energy storage capacity combined with supercapacitor-like power handling(Cambridge : RSC Publ., 2016) Lee, Juhan; Krüner, Benjamin; Tolosa, Aura; Sathyamoorthi, Sethuraman; Kim, Daekyu; Choudhury, Soumyadip; Seo, Kum-Hee; Presser, VolkerWe introduce a high performance hybrid electrochemical energy storage system based on an aqueous electrolyte containing tin sulfate (SnSO4) and vanadyl sulfate (VOSO4) with nanoporous activated carbon. The energy storage mechanism of this system benefits from the unique synergy of concurrent electric double-layer formation, reversible tin redox reactions, and three-step redox reactions of vanadium. The hybrid system showed excellent electrochemical properties such as a promising energy capacity (ca. 75 W h kg−1, 30 W h L−1) and a maximum power of up to 1.5 kW kg−1 (600 W L−1, 250 W m−2), exhibiting capacitor-like galvanostatic cycling stability and a low level of self-discharging rate.