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Sökning: WFRF:(Andersson Arne)

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1.
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2.
  • Andersson, Arne, et al. (författare)
  • Direct Propane Ammoxidation to Acrylonitrile: Kinetics and Nature of the Active Phase
  • 1993
  • Ingår i: New Frontiers in Catalysis (Studies in Surface Science and Catalysis ). - 0167-2991. ; 75, s. 691-705
  • Konferensbidrag (refereegranskat)abstract
    • The kinetics of the direct synthesis of acrylonitrile from propane on V-Sb-Al-(W) mixed oxides indicate that acrylonitrile (ACN) forms by two parallel pathways, one directly from propane and the second, which is the prevalent path, through the intermediate formation of propylene (C3=). The limiting factor in the formation of ACN is the relative slowness of the step of allylic oxidation to ACN of the intermediate C3=, and the higher rate of C3= oxidation to carbon oxides as compared to that of ACN to COx. The step of C3= oxidation to ACN is controlled by the surface availability of NH3 which, in turn, depends considerably on the side reaction of NH3 oxidation to N2. The catalytic behavior of different modified V-Sb-(Al)-O systems and their characterization by X-ray diffraction analysis and Raman, Infrared and X-ray Photoelectron spectroscopies indicate that i) a reduction of both V and Sb occurs during the catalytic reaction, ii) the presence of vanadium not stabilized in the rutile-like phase is responsible for the side reaction of NH3 oxidation and lowering of the selectivity, iii) alumina reacts with antimony forming an AlSbO4 rutile phase which could be epitaxially intergrown or in solid solution with the VSbO4/Sb2O4 system, which, in turn, limits the presence of not stabilized (unselective) vanadium species, and iv) antimony oxide supported on alumina is also selective in propane ammoxidation, but forming acetonitrile as the main product. The doping with vanadium of this sample increases slightly the activity, but especially gives rise to the formation of acrylonitrile instead of acetonitrile.
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3.
  • Andersson, Arne, et al. (författare)
  • Surface Characterization and Reactivity in Ammoxidation Reactions of Vanadium Antimonate Catalysts
  • 1994
  • Ingår i: Applied Catalysis A: General. - 0926-860X. ; 113:1, s. 43-57
  • Tidskriftsartikel (refereegranskat)abstract
    • Unsupported vanadium antimonate catalysts with Sb/V ratios of 1 and 5 and samples with the latter ratio supported on alumina were studied in toluene and propane ammoxidation to benzonitrile and acrylonitrile, respectively, and were characterized by X-ray photoelectron spectroscopy (XPS) analysis before and after catalytic tests. Activity data for toluene ammoxidation suggest that excess antimony with respect to the stoichiometric amount required for forming the VSbO4 rutile phase affects the dispersion of the latter phase giving smaller particles. Vanadium sites are involved both in the activation of toluene and in the insertion of nitrogen in this reaction, whereas antimony does not play a specific role in the reaction mechanism. In propane ammoxidation, on the other hand, due to a higher reaction temperature with respect to toluene (500°C vs. 370°C), free vanadia on the surface of the catalyst has a negative influence on the selectivity because it promotes the conversion of ammonia to nitrogen, decreasing the surface nitrogenous species required for the selective formation of acrylonitrile. Excess antimony is thus necessary for completing the reaction between antimony and vanadium oxides, but antimony also participates in the reaction mechanism. In propane ammoxidation, in fact, XPS data show that both vanadium and antimony sites are reduced. Tentatively, vanadium sites are involved in the activation of propane, while antimony sites insert nitrogen. The differences between the toluene and propane ammoxidation mechanisms are interpreted to be primarily related to the different reaction temperatures.
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4.
  • Andersson, John Åke, et al. (författare)
  • Sweden's Economic Relationships with Uganda
  • 2016
  • Rapport (övrigt vetenskapligt/konstnärligt)abstract
    • This explorative study aims to map commercial and other economic relations between Sweden and Uganda during the years 2000-2014. In addition, we will discuss whether and how these relations may be related to Swedish bilateral aid.
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5.
  • Baranowska Körberg, Izabella, et al. (författare)
  • A Simple Repeat Polymorphism in the MITF-M Promoter Is a Key Regulator of White Spotting in Dogs
  • 2014
  • Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 9:8, s. e104363-
  • Tidskriftsartikel (refereegranskat)abstract
    • The white spotting locus (S) in dogs is colocalized with the MITF (microphtalmia-associated transcription factor) gene. The phenotypic effects of the four S alleles range from solid colour (S) to extreme white spotting (s(w)). We have investigated four candidate mutations associated with the s(w) allele, a SINE insertion, a SNP at a conserved site and a simple repeat polymorphism all associated with the MITF-M promoter as well as a 12 base pair deletion in exon 1B. The variants associated with white spotting at all four loci were also found among wolves and we conclude that none of these could be a sole causal mutation, at least not for extreme white spotting. We propose that the three canine white spotting alleles are not caused by three independent mutations but represent haplotype effects due to different combinations of causal polymorphisms. The simple repeat polymorphism showed extensive diversity both in dogs and wolves, and allele-sharing was common between wolves and white spotted dogs but was non-existent between solid and spotted dogs as well as between wolves and solid dogs. This finding was unexpected as Solid is assumed to be the wild-type allele. The data indicate that the simple repeat polymorphism has been a target for selection during dog domestication and breed formation. We also evaluated the significance of the three MITF-M associated polymorphisms with a Luciferase assay, and found conclusive evidence that the simple repeat polymorphism affects promoter activity. Three alleles associated with white spotting gave consistently lower promoter activity compared with the allele associated with solid colour. We propose that the simple repeat polymorphism affects cooperativity between transcription factors binding on either flanking sides of the repeat. Thus, both genetic and functional evidence show that the simple repeat polymorphism is a key regulator of white spotting in dogs.
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6.
  • Huuhtanen, Jane, et al. (författare)
  • Catalytic and Spectroscopic Studies of Vanadium Oxide Supported on Group IVb and Vb Metal Oxides for Oxidation of Toluene
  • 1993
  • Ingår i: Applied Catalysis A: General. - 0926-860X. ; 97:2, s. 197-221
  • Tidskriftsartikel (refereegranskat)abstract
    • Vanadia was deposited on TiO2, ZrO2, HfO2, Nb2O5, and Ta2O5 supports using impregnation with either an oxalic acid solution of NH4VO3 or a solution of vanadyl acetylacetonate in ethanol. Prepared samples, with a nominal vanadia content in the range 0.5–2 monolayers, were characterized with X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman and infrared spectroscopy, and were used in toluene oxidation. XRD did not reveal formation of any vanadia phase. XPS spectra showed deposited vanadium to be present mainly as V5+ on all the supports. A plot of the V:( support metal) ratio determined by XPS showed agglomeration of vanadia on TiO2, ZrO2, HfO2, and Nb2O5 to occur at loadings above 0.5 monolayer, while for Ta2O5 the dispersion seemed independent of the loading. Preparations from vanadyl acetylacetonate gave superior dispersion. Raman spectra showed bands from crystalline V2O5 on all the supports except Nb2O5. Raman and infrared bands from dispersed vanadia were present in the spectra of TiO2 (three species), ZrO2 and HfO2 (both one species) supported catalysts. No bands from vanadium-oxygen vibrational modes were seen in the spectra of Nb2O5 supported samples, but a V-OH band was observed, suggesting an amorphous structure. Some evidence was obtained for formation of amorphous VTa9O25 on Ta205. The activity for toluene oxidation increased with vanadia loading for each support, and the activity varied with respect to support at all loadings in the order TiO2 > ZrO2 > Nb2O5 > HfO2 > Ta2O5. The selectivity for formation of benzaldehyde was the highest using TiO2 and Nb2O5 supports, while for benzoic acid TiO2 was the best support.
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7.
  • Lundgren, Marcus, et al. (författare)
  • Lift-Off Lengths in an Optical Heavy-Duty Engine Operated at High Load with Low and High Octane Number Fuels
  • 2018
  • Ingår i: SAE Technical Papers. - 400 Commonwealth Drive, Warrendale, PA, United States : SAE International. - 0148-7191. ; 2018-April
  • Tidskriftsartikel (refereegranskat)abstract
    • The influence of the ignition quality of diesel-and gasoline-like fuels on the lift-off length of the jet were investigated in an optical heavy duty engine. The engine was operated at a load of 22 bar IMEPg and 1200 rpm. A production type injector with standard holes were used. The lift-off length was recorded with high speed video Different injection pressures and inlet temperatures were used to affect conditions that consequently affect the lift-off length. No matter which fuel used nor injection pressure or inlet temperature, all lift-off lengths showed equal or close to equal lift-off length when stabilized. The higher octane fuel had a longer ignition delay and therefore the fuel penetrate the combustion chamber before auto ignition. This gave a longer lift-off length at the initial stage of combustion before reaching the same stabilized lift-off length. These results indicate that the hot combustion gases are a dominant factor to the lift-off length. Also, that possible soot reductions using high octanes fuels are feasible because of a longer ignition delay that allow more premixing, and an initially longer lift-off length due to longer penetration into the combustion chamber.
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8.
  • Lundgren, Marcus Olof, et al. (författare)
  • Effects of Post-Injections Strategies on UHC and CO at Gasoline PPC Conditions in a Heavy-Duty Optical Engine
  • 2017
  • Ingår i: SAE Technical Papers. - 400 Commonwealth Drive, Warrendale, PA, United States : SAE International. - 0148-7191. ; 2017:March
  • Tidskriftsartikel (refereegranskat)abstract
    • Gasoline partially premixed combustion (PPC) has shown potential in terms of high efficiency with low emissions of oxides of nitrogen (NOx) and soot. Despite these benefits, emissions of unburned hydrocarbons (UHC) and carbon monoxide (CO) are the main shortcomings of the concept. These are caused, among other things, by overlean zones near the injector tip and injector dribble. Previous diesel low temperature combustion (LTC) research has demonstrated post injections to be an effective strategy to mitigate these emissions. The main objective of this work is to investigate the impact of post injections on CO and UHC emissions in a quiescent (non-swirling) combustion system. A blend of primary reference fuels, PRF87, having properties similar to US pump gasoline was used at PPC conditions in a heavy duty optical engine. The start of the main injection was maintained constant. Dwell and mass repartition between the main and post injections were varied to evaluate their effect. All points were run at 7 bar IMEPg. High-speed imaging of the natural combustion luminescence was performed together with measurements of performance and engine out emissions. Results show reduction in both CO and UHC with close coupled injections. A large close coupled post injection show the largest reduction in UHC. Analysis show that a post injection prior to combustion reduces the dribble and increases the recirculation in the downstream region of the fuel jet, hence reaching more of the UHC in the area near the injector. General observations show that the partition of fuel between the injections have the largest impact on the CO while the dwell time affects UHC emissions. Injector dribble seems to be a significant contributor to the UHC emissions.
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9.
  • Lundgren, Marcus, et al. (författare)
  • Optical study on combustion transition from HCCI to PPC with gasoline compression ignition in a HD engine
  • 2016. - April
  • Ingår i: SAE 2016 World Congress and Exhibition. - 400 Commonwealth Drive, Warrendale, PA, United States : SAE International. ; 2016-April
  • Konferensbidrag (refereegranskat)abstract
    • The partially premixed combustion (PPC) concept has shown high efficiency with low soot emissions. However, the in-cylinder phenomena are still to be explained and evaluated for further progress in the research. This work studies the start of combustion process during a transition from homogenous charge compression ignition (HCCI) to PPC. The process is visualized using a heavy-duty, non-swirling engine modified for optical access. High speed video was used to capture the natural luminosity of the combustion. The fuel used was PRF87. Single and double injection strategies were used at a load kept to the moderate level of 7.5 bar IMEPg. Single injections were swept from early HCCI to retarded PPC conditions whilst running a cycle to cycle temperature sweep, to capture the effect of injection timing and temperature differences simultaneously. Results show that retarded injections show less cycle-to-cycle variation due to temperature variations. Advanced in-bowl injections show a stochastic behavior in the location of the first combustion, due to large variations in local fuel rich zones. For the double injection case the main injection cools the bulk temperature and hence delays the start of combustion before igniting in the fuel rich zones.
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10.
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