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Sökning: WFRF:(Hedin Niklas)

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1.
  • Abebe, Mihret, et al. (författare)
  • Spherical and Porous Particles of Calcium Carbonate Synthesized with Food Friendly Polymer Additives
  • 2015
  • Ingår i: Crystal Growth & Design. - : American Chemical Society (ACS). - 1528-7483 .- 1528-7505. ; 15:8, s. 3609-3616
  • Tidskriftsartikel (refereegranskat)abstract
    • Porous calcium carbonate particles were synthesized by adding solutions of Ca2+ to solutions of CO32- containing polymeric additives. Under optimized conditions well-defined aggregates of the anhydrous polymorph vaterite formed. A typical sample of these micrometer-sized aggregates had: a pore volume of 0.1 cm(3)/g, a pore width of similar to 10 nm, and a specific surface area of similar to 25-30 m(2)/ g. Only one mixing Order (calcium to carbonate) allowed the formation of vaterite, which was ascribed to the buffering capacity and relatively high pH of the CO32- solution. Rapid addition of the calcium chloride solution and rapid stirring promoted the formation of vaterite, due to the high supersaturation levels achieved. With xanthan gum, porous and micrometer-sized vaterite aggregates could be synthesized over a wide range of synthetic conditions. For the Other food grade polymers, hydroxypropyl methylcellulose (HPMC), methylcellulose (MC), and sodium carboxyl methylcellulose, several intensive and extensive synthetic parameters had to be optimized to obtain pure vaterite and porous aggregates. HPMC and MC allowed well-defined spherical micrometer-sited particles to form. We expect that these spherical and porous particles of vaterite could be relevant to model studies as well as a controlled delivery of particularly large molecules.
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2.
  • Akhtar, Farid, et al. (författare)
  • Aluminophosphate monoliths with high CO2-over-N2 selectivity and CO2 capture capacity
  • 2014
  • Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 4:99, s. 55877-55883
  • Tidskriftsartikel (refereegranskat)abstract
    • Monoliths of microporous aluminophosphates (AlPO4-17 and AlPO4-53) were structured by binder-free pulsed current processing. Such monoliths could be important for carbon capture from flue gas. The AlPO4-17 and AlPO4-53 monoliths exhibited a tensile strength of 1.0 MPa and a CO2 adsorption capacity of 2.5 mmol g-1 and 1.6 mmol g-1, respectively at 101 kPa and 0°C. Analyses of single component CO2 and N2 adsorption data indicated that the AlPO4-53 monoliths had an extraordinarily high CO2-over-N2 selectivity from a binary gas mixture of 15 mol% CO2 and 85 mol% N2. The estimated CO2 capture capacity of AlPO4-17 and AlPO4-53 monoliths in a typical pressure swing adsorption (PSA) process at 20°C was higher than that of the commonly used zeolite 13X granules. Under cyclic sorption conditions, AlPO4-17 and AlPO4-53 monoliths were regenerated by lowering the pressure of CO2. Regeneration was done without application of heat, which would regenerate them to their full capacity for CO2 adsorption.
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3.
  • Akhtar, Farid, et al. (författare)
  • Strong and binder free structured zeolite sorbents with very high CO2-over-N-2 selectivities and high capacities to adsorb CO2 rapidly
  • 2012
  • Ingår i: Energy & Environmental Science. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 5:6, s. 7664-7673
  • Tidskriftsartikel (refereegranskat)abstract
    • Mechanically strong monoliths of zeolite NaKA with a hierarchy of pores displayed very high CO2-over-N-2 selectivity. The zeolite monoliths were produced by pulsed current processing (PCP) without the use of added binders and with a preserved microporous crystal structure. Adsorption isotherms of CO2 and N-2 were determined and used to predict the co-adsorption of CO2 and N-2 using ideal adsorbed solution theory (IAST). The IAST predictions showed that monolithic adsorbents of NaKA could reach an extraordinarily high CO2-over-N-2 selectivity in a binary mixture with a composition similar to flue gas (15 mol% CO2 and 85 mol% N2 at 25 degrees C and 101 kPa). Structured NaKA monoliths with a K+ content of 9.9 at% combined a CO2-over-N-2 selectivity of >1100 with a high CO2 adsorption capacity (4 mmol g(-1)) and a fast adsorption kinetics (on the order of one minute). Estimates of a figure of merit (F) based on IAST CO2-over-N-2 selectivity, and time-dependent CO2 uptake capacity, suggest that PCP-produced structured NaKA with a K+ content of 9.9 at% offers a performance far superior to 13X adsorbents, in particular at short cycle times.
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6.
  • Akhtar, Farid, et al. (författare)
  • Structuring adsorbents and catalysts by processing of porous powders
  • 2014
  • Ingår i: Journal of the European Ceramic Society. - : Elsevier BV. - 0955-2219 .- 1873-619X. ; 34:7, s. 1643-1666
  • Tidskriftsartikel (refereegranskat)abstract
    • Microporous materials such as zeolites, metal organic frameworks, activated carbons and aluminum phosphates are suitable for catalysis and separation applications. These high surface area materials are invariably produced in particulate forms and need to be transformed into hierarchically porous structures for high performance adsorbents or catalysts. Structuring of porous powders enables an optimized structure with high mass transfer, low pressure drop, good heat management, and high mechanical and chemical stability. The requirements and important properties of hierarchically porous structures are reviewed with a focus on applications in gas separation and catalysis. Versatile powder processing routes to process porous powders into hierarchically porous structures like extrusion, coatings of scaffolds and honeycombs, colloidal processing and direct casting, and sacrificial approaches are presented and discussed. The use and limitations of the use of inorganic binders for increasing the mechanical strength is reviewed, and the most important binder systems, e.g. clays and silica, are described in detail. Recent advances to produce binder-free and complex shaped hierarchically porous monoliths are described and their performance is compared with traditional binder-containing structured adsorbents. Needs related to better thermal management and improved kinetics and volume efficiency are discussed and an outlook on future research is also given.
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8.
  • Antonsson, Kjell, et al. (författare)
  • Occurrence of the hermit beetle (Osmoderma eremita), in Sweden.
  • 2003
  • Ingår i: Entomologisk tidskrift. - 0013-886X. ; 124:4, s. 225-240
  • Tidskriftsartikel (refereegranskat)abstract
    • We have compiled data on the occurrence of a threatened beetle, Osmoderma eremita, in Sweden. The species inhabits tree hollows with wood mould. The data were compiled from field surveys conducted in 1993-2003, using pitfall traps at 401 localities and using wood mould sampling at 104 localities. We have also gone through published data and all larger Swedish museums and registered old records. O. eremita was recorded at about 30% of the field surveys. In Sweden, oak is by far the most important host tree species, but the beetle has also been found in other deciduous trees, such as beech, alder, ash and lime. Currently, 270 localities with Osmoderma eremita, defined as records of living adults, larvae, fragments of adult body parts, or excrements situated at least 1 km from each other, are known in Sweden. 129 of these localities are records of live beetles or larvae made after 1990. The species is found in the southern third of Sweden only, and there are more localities in the eastern part compared to the western. The great majority of the localities have been discovered during the last ten years. At some of the localities only excrements or fragments have been recorded, and the species might actually be extinct at some of these localities. Due to low search intensity historically, it is impossible to use these data to discover any changes in the distribution or occurrence over time. Because old, hollow oaks were much more frequent 200 years ago, we suggest that the species has decreased severely in Sweden since that time. Today, old oaks are rarely cut down but instead lack of grazing cattle is a threat because many sites regrow with dense tree stands which outcompete the old hollow trees. Many local extinctions could also be expected during the next few decades, because many of the localities have too few hollow trees and are too isolated. At many localities, lack of younger trees which can take over the role as host trees when the present trees die will also be a problem in the future.
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9.
  • Arauzo, P. J., et al. (författare)
  • Assessment of the effects of process water recirculation on the surface chemistry and morphology of hydrochar
  • 2020
  • Ingår i: Renewable energy. - : Elsevier BV. - 0960-1481 .- 1879-0682. ; 155, s. 1173-1180
  • Tidskriftsartikel (refereegranskat)abstract
    • The effect of two process water (PW) recirculation strategies after hydrothermal carbonization (HTC) of brewers spent grains (BSG) is evaluated with the focus on the hydrochar characteristics. The HTC process has been carried out under different operating conditions, which are residence time between 2 and 4 h and temperature in the range of 200-220 degrees C. The composition of the hydrochars reveals that operating conditions have a more significant effect than PW recirculation. The composition of the liquid produced by HTC with PW recirculation is essentially controlled by the operating temperature, for instance, the total organic carbon (TOC) in the PW changes in the narrow range of 200-220 degrees C. A detailed analysis of PW also has been done. The main components of the liquid phase are lactic, formic, acetic, levulinic, and propionic acid as well as 5-hydroxymethylfurfural, that affect the surface structure of the hydrochars.
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10.
  • Atluri, Rambabu, 1981-, et al. (författare)
  • Hydrothermal Phase Transformation of Bicontinuous Cubic Mesoporous Material AMS-6
  • 2008
  • Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 20:12, s. 3857–3866-
  • Tidskriftsartikel (refereegranskat)abstract
    • The controlled synthesis of ordered anionic surfactant templated mesoporous silica with cubic Ia3d̅ structure (AMS-6) is reported via prolonged periods of hydrothermal treatment (HT). The cubic Ia3d̅ mesophase transforms to hexagonal p6mm after 8 days of HT at 100 °C. Surprisingly, the hexagonal phase is stable only for a limited period after which a reversal to the cubic Ia3d̅ mesostructure is observed. Characterization methods such as powder X-ray diffraction (XRD), electron microscopy (SEM, TEM), N2-isotherms, magic-angle spinning (MAS) 29Si NMR spectroscopy, and thermogravimetric analysis (TGA) have been employed to follow structural and textural changes of the materials prepared. Data show that the resultant mesostructure and its textural properties are highly dependent on the period of HT with less unit-cell shrinkage on calcination after extensive HT. Furthermore, evidence of two different solid−solid phase mechanisms during HT is presented. The initial transition is consistent with a restructuring of the surfactant packing and a depletion of the organic moieties from the organo-silica wall as evident from 29Si NMR spectroscopy. The return to the bicontinuous cubic phase is driven by changes in charge matching at the organic−inorganic interface as a result of increases in the polymerization of the silica wall. The textural properties, and in particular the presence or absence of surface porosity, has been controlled through variations in hydrothermal treatment. These are associated with specific growth directions of cubic AMS-6 crystals. The synthetic method described allows us to easily prepare phase pure and intermediate mesostructured nanoparticles.
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