Activation of Cobalt Foil Catalysts for CO Hydrogenation

CO hydrogenation has been studied on cobalt foils as model catalysts for Fischer–Tropsch (FT) synthesis. The effect of pretreatment (number of calcinations and different reduction times) for cobalt foil catalysts at 220 °C, 1 bar, and H2/CO = 3 has been studied in a microreactor. The foils were examined by scanning electron microscopy (SEM). It was found that the catalytic activity of the cobalt foil increases with the number of pretreatments. The mechanism is likely an increase in the available cobalt surface area from progressively deeper oxidation of the foil, supported by surface roughness detected by SEM. The highest FT activity was obtained using a reduction time of only 5 min (compared to 1 and 30 min). Prolonged reduction caused the sintering of cobalt crystallites, while too short of a reduction time led to incomplete reduction and small crystallites susceptible to low turn-over frequency from structure sensitivity. Larger crystals from longer reduction times gave increased selectivity to heavier components. The paraffin/olefin ratio increased with the increasing number of pretreatments due to olefin hydrogenation favored by enhanced cobalt site density. From the results, it is suggested that olefin hydrogenation is not structure sensitive, and that mass transfer limitations may occur depending on the pretreatment procedure. Produced water did not influence the results for the low conversions experienced in the present study (<6%).

Decoding Complexity in Structure-Sensitive Reactions

Structure-sensitive reactions involving the Mars and van Krevelen mechanism over metal and metal oxide catalysts are ubiquitous in reaction kinetics and engineering. The kinetic equations of such reactions are re-written to account for modern operando spectroscopy and microscopy observations. Emphasis is placed on reactions with nucleophilic (lattice) oxygen, oxygen reduction reversibility, an interconversion scheme, non-linear water adsorption, remote-control model, and non-uniform sites. The multiplicity of propane conversion over MoVTeNbOx catalysts is proven through a combination of non-linear competitive water adsorption, the presence of multiple active sites, a re-structuring active site, and oxygen adsorption. The modified remote-control kinetics for the Mars and van Krevelen mechanism can account for the observations of steady-state multiplicities and hysteresis. The results have implications for improving catalytic activity, reducing operating process costs, and active site engineering of selective oxidation catalysis.

Dynamic restructuring of supported metal nanoparticles and its implications for structure insensitive catalysis

Some fundamental concepts of catalysis are not fully explained but are of paramount importance for the development of improved catalysts. An example is the concept of structure insensitive reactions, where surface-normalized activity does not change with catalyst metal particle size. Here we explore this concept and its relation to surface reconstruction on a set of silica-supported Ni metal nanoparticles (mean particle sizes 1–6 nm) by spectroscopically discerning a structure sensitive (CO2 hydrogenation) from a structure insensitive (ethene hydrogenation) reaction. Using state-of-the-art techniques, inter alia in-situ STEM, and quick-X-ray absorption spectroscopy with sub-second time resolution, we have observed particle-size-dependent effects like restructuring which increases with increasing particle size, and faster restructuring for larger particle sizes during ethene hydrogenation while for CO2 no such restructuring effects were observed. Furthermore, a degree of restructuring is irreversible, and we also show that the rate of carbon diffusion on, and into nanoparticles increases with particle size. We finally show that these particle size-dependent effects induced by ethene hydrogenation, can make a structure sensitive reaction (CO2 hydrogenation), structure insensitive. We thus postulate that structure insensitive reactions are actually apparently structure insensitive, which changes our fundamental understanding of the empirical observation of structure insensitivity.

Thermo-Oxidative Destruction and Biodegradation of Nanomaterials from Composites of Poly(3-hydroxybutyrate) and Chitosan

A complex of structure-sensitive methods of morphology analysis was applied to study film materials obtained from blends of poly(3-hydroxybutyrate) (PHB) and chitosan (CHT) by pouring from a solution, and nonwoven fibrous materials obtained by the method of electrospinning (ES). It was found that with the addition of CHT to PHB, a heterophase system with a nonequilibrium stressed structure at the interface was formed. This system, if undergone accelerated oxidation and hydrolysis, contributed to the intensification of the growth of microorganisms. On the other hand, the antimicrobial properties of CHT led to inhibition of the biodegradation process. Nonwoven nanofiber materials, since having a large specific surface area of contact with an aggressive agent, demonstrated an increased ability to be thermo-oxidative and for biological degradation in comparison with film materials.

Effect of External Impacts on the Structure and Martensitic Transformation of Rapidly Quenched TiNiCu Alloys

TiNi-TiCu quasibinary system alloys with a high Cu content produced by rapid quenching from liquid state in the form of thin amorphous ribbons exhibit pronounced shape memory effect after crystallization and are promising materials for miniaturized and fast operating devices. There is currently no complete clarity of the mechanisms of structure formation during crystallization from the amorphous state that determine the structure-sensitive properties of these alloys. This work deals with the effect of the initial amorphous state structure and crystallization method of the alloys on their structure and phase transformations. To this end the alloy containing 30 at.% Cu was subjected to thermal and mechanical impact in the amorphous state and crystallized using isothermal or electropulse treatment. We show that after all types of treatment in the amorphous state the structure of the alloy remains almost completely amorphous but the characteristic temperatures and enthalpy of crystallization become slightly lower. Isothermal crystallization of alloy specimens produces a submicrocrystalline structure with an average grain size in the 0.4–1.0 μm range whereas electropulse crystallization generates a bimorphic structure consisting of large 4–6 μm grains and 2–3 μm high columnar crystals in the vicinity of the surface. The grains have nanosized plate-like and subgrain structures. The largest grains are observed in thermally activated samples, meanwhile, mechanical impact in the amorphous state leads to the formation of equiaxed finer grains with a less defective subgrain structure and to the shift of the temperature range of the martensitic transformation toward lower temperatures.

Structure-sensitive testimonial norms

Although there has been a lot of investigation into the influence of the network structure of scientific communities on the one hand and into testimonial norms (TNs) on the other, a discussion of TNs that take the network structure into account has been lacking. In this paper, I introduce two TNs which are sensitive to the local network structure. According to these norms, scientists should give less weight to the results of well-connected colleagues, as compared to less connected ones. I employ an Agent Based Model to test the reliability of the two novel TNs against different versions of conventional, structure-insensitive TNs in networks of varying size and structure. The results of the simulations show that the novel TNs are more reliable. This suggests that it would be beneficial for scientific communities if their members followed such norms. For individual scientists, I show that there are both reasons for and reasons against adopting them.

Levels of Ontology and Natural Language

Two levels of ontology are commonly distinguished in metaphysics: the ontology of ordinary objects, or more generally ordinary ontology, and the ontology of what there really or fundamentally is. This chapter argues that natural language reflects not only the ordinary ontology but also a language-driven ontology, which is involved in the mass-count distinction and part-structure-sensitive semantic selection (as well as perhaps the light ontology of pleonastic entities in the sense of Schiffer). The language-driven ontology does not constitute another level of representation, but is taken to be a (selective) ontology of the real, given a plenitudinous or maximalist conception of reality. The language-driven ontology aligns closely with the functional part of grammar and a commitment to it is mandatory with the use of language. This gives rise to a novel view according to which part of ontology should be considered part of universal grammar on a broadened understanding. The chapter recasts the author’s older theory of situated part structures without situations, in purely ontological terms, making use of a primitive notion of unity.