Influence of potassium and NO addition on catalytic activity in soot combustion and surface properties of iron and manganese spinels

Two series of (0–4 wt%) potassium doped oxide catalysts based on iron and manganese spinel were prepared. The synthesized materials were characterized in terms of their structure (XRD, Raman spectroscopy) and surface electronic properties (work function measurements). The catalytic activity towards soot combustion was determined by temperature programmed oxidation of a physical mixture of soot and catalyst in tight contact in gas oxygen mixtures with and without NO addition. For iron spinel based mate- rials, where potassium is localized at the surface, the cata- lytic activity correlates with the work function lowering upon K doping, while for manganese spinel based materials, where potassium is incorporated into the bulk (formation of KMn 4 O 8 or KMn 8 O 16 ), the correlation was not found. The presence of NO in the gas mixture leads to a systematic decrease of soot ignition temperature for all samples

Role of electronic factor in soot oxidation process over tunnelled and layered potassium iron oxide catalysts

This paper describes the investigations of the catalytic activity in soot oxidation over well-defined iron oxide based materials. The nanostructuration of iron oxide by potassium into tunnelled (KFeO 2 ) and layered (K 2 Fe 22 O 34 ) ferrites and the surface promotion with CeO 2 results in the marked increase in the catalytic activity (decrease of the ignition temperature down to 210 ° C and T 10 % to 310 ° C). The measurements of the catalysts work function showed that both nanostructuration and surface promotion with ceria of the best KFeO 2 phase led to increase of the electron availability (decrease of the work function). Strong correlation of the catalytic activity in soot combustion of the Ce–K–Fe–O systems with the work function value was revealed for the first time in the model studies, and can be used as a guideline for optimisation of the real catalytic filters

Functionalization of graphite with oxidative plasma

Surface-modified graphite is studied as an electrode material, an adsorbent, and a membrane component, among other applications. Modifying the graphite with plasma can be used to create relevant surface functionalities, in particular, various oxygen groups. The application of surface-oxidized graphite often requires its use in an aqueous environment. The application in an aqueous environment is not an issue for acid-oxidized carbons, but a discrepancy in the structure–activity relationship may arise because plasma-oxidized carbons show a time-dependent decrease in the degree of functionalization and related properties. Moreover, plasma-oxidized materials are often characterized in terms of their chemical and physical properties, most notably their degree of functionalization after plasma treatment, without contact with water. In this study, we used low-temperature plasma oxidation with pure oxygen and carbon dioxide and sample-washing with concentrated nitric and sulfuric acids. To evaluate the electronic properties of modified graphite, the work function changes and surface oxygen content were measured just after plasma modification and after water immersion. We show that water immersion drastically decreases the work function of plasma-treated samples, which is accompanied by a decrease in the number of radicals introduced by plasma. Our results demonstrate that the increase in stable work function as a result of plasma treatment, brought about by an increase in the surface oxygen species concentration, can be realized most effectively for the acid-washed graphite

The effect of Fe, Co, and Ni structural promotion of cryptomelane (KMn8O16)(KMn_8O_{16}) on the catalytic activity in oxygen evolution reaction

Transition metal (Fe, Co, Ni)-doped cryptomelane materials (K-OMS-2) were synthesized and characterized with the use of XRD, Raman spectroscopy, XPS, N2-BET, H2-TPR, and SEM. The electrocatalytic reactivity in oxygen evolution was evaluated with the use of the rotating disk electrode. It was found that the electrocatalytic activity is substantially enhanced for the cobaltdoped material, while iron and nickel doping have no, or even, negative effect on K-OMS-2. The structure of the material bulk is preserved in all cases, but the formation of additional birnessite phases can be evidenced for the iron and cobalt dopants. It is discussed that the reactivity enhancement of Co/K-OMS-2 can be related not only to the formation of cobalt-doped heterophases (cobaltane, birnessite) but also to the changes of the properties of pristine cryptomelane