Controlling chirality in growth of single-walled carbon nanotubes (SWNTs) is important for exploiting their practical applications. For long it has been conceptually conceived that the structural control of SWNTs is potentially achievable by fabricating nanoparticle catalysts with proper structures on crystalline substrates via epitaxial growth techniques. Here, we have accomplished epitaxial formation of monometallic Co nanoparticles with well-defined crystal structure, and its use as a catalyst in the selective growth of SWNTs. Dynamics of Co nanoparticles formation and SWNT growth inside an atomic-resolution environmental transmission electron microscope at a low CO pressure was recorded. We achieved highly preferential growth of semiconducting SWNTs (~90%) with an exceptionally large population of (6, 5) tubes (53%) in an ambient CO atmosphere. Particularly, we also demonstrated high enrichment in (7, 6) and (9, 4) at a low growth temperature. These findings open new perspectives both for structural control of SWNTs and for elucidating the growth mechanisms.

Zirconium oxide (ZrO2, zirconia) is an interesting catalytic material to be used in biomass conversion, e.g., gasification and reforming. In this work, we show that reducing and hydrating pretreatments affect the surface sites on monoclinic zirconia. The multitechnique approach comprises temperature-programmed surface reactions (TPSR) under CO and CO2 at 100-550 °C, in situ DRIFTS investigations of the surface species and density functional theory (DFT) calculations. The key findings of the work are: (1) formates are formed either directly from gas-phase CO on terminal surface hydroxyls or via the linear CO surface species that are found exclusively on the reduced zirconia without water treatment; (2) formates are able to decompose at high temperature either reversibly to CO or reductively to CO2 and H2via surface reaction between formates and multicoordinated hydroxyls; and (3) a new weak reversible binding state of CO is found exclusively on ZrO2 that is first reduced and subsequently hydrated.

Catalytic fast pyrolysis of pine sawdust was successfully carried out in VTT's 20 kg h −1 Process Development Unit using a spray dried HZSM-5 catalyst. Approximately 250 kg of partially deoxygenated pyrolysis oil was produced over a period of four days. The catalytically produced pyrolysis oil had an average moisture content of 8.3 wt%, and average carbon and oxygen contents of 72.0 and 21.5 wt% on a dry basis, respectively. Approximately 24% of the original biomass carbon was present in the pyrolysis oil, whereas 14% of carbon was in the form of aqueous side products, which totaled approximately 600 kg. The pyrolysis oil contained a high amount of lignin derived water-insoluble material, as well as 6.4 wt% of aromatic hydrocarbons. The majority of the carbohydrate derived products, i.e. acids, aldehydes, ketones and sugar-type compounds, were found in the aqueous product fraction. While the quality of pyrolysis oil remained quite stable during the four day experiment, distinct changes were observed in the properties and the behavior of the catalyst. Coke formation was heaviest at the beginning of the experiment, and then subsided over time. Catalyst micropore area and volume also decreased during the experiment. This transformation was accompanied by apparent changes in the crystallinity and the structure of the catalyst. Scanning electron microscope images of the catalyst also revealed clear physical damage to the particles. Biomass alkali metals also deposited on the catalyst, and the spent catalyst contained a total of 1.1 wt% of Ca, K, Mg and P after the experiment. A linear correlation was observed between catalyst alkali metal content and acidity, which indicated that biomass alkalis substituted the proton functionalities of the HZSM-5 acid sites. † Electronic supplementary information (ESI) available. See

No abstract

No abstract