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Sökning: (WFRF:(Nilsson Patrik)) srt2:(2000-2004) > (2003)

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1.
  • Almefelt, Lars, 1968, et al. (författare)
  • Exploring Requirements Management in the Automotive Industry
  • 2003
  • Ingår i: 14th International Conference on Engineering Design Research for Practice - innovative products, processes and organisations.
  • Konferensbidrag (refereegranskat)abstract
    • This paper presents an empirical study carried out in the automotive industry, with the aim to bring forward new experiences and knowledge on management of requirements in practice. Adopting a qualitative systems approach, and using multiple information sources, the requirements management process during the development of a passenger car cockpit has been mapped out. The logical reconstruction of the requirements management process is complemented with descriptions of associated phenomena, such as important events and attitudes. Findings are presented, analysed and discussed considering also factors underlying observed phenomena.
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2.
  • Fiedler, Markus, et al. (författare)
  • Identification of performance degradation in IP networks using throughput statistics
  • 2003
  • Konferensbidrag (refereegranskat)abstract
    • To be able to satisfy their users, interactive applications like video conferences require a certain Quality-of-Service from heterogeneous networks. This paper proposes the use of throughput histograms as Quality-of-Service indicator. These histograms are built from local, unsynchronized, passive measurements of packet streams from the viewpoint of an application. They can easily be exchanged between sender and receiver, and their comparison provides information about severity and type of a potential bottleneck. We demonstrate the usefulness of these indicators for evaluating the transport quality perceived by a video conferencing application and its users in the presence of a bottleneck.
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4.
  • Nilsson, Patrik, et al. (författare)
  • Synthesis, structure, and reactivity of arylfluoro platinum(II) complexes.
  • 2003
  • Ingår i: Organometallics. - : American Chemical Society (ACS). - 1520-6041 .- 0276-7333. ; 22:25, s. 5235-5242
  • Tidskriftsartikel (refereegranskat)abstract
    • Complexes of the type trans-[PtPhFL2], where L = PPh3 (4), PMe2Ph (5), were synthesized. Complex 4 was characterized by X-ray crystallography. The equilibrium constant for the substitution of the fluoride trans to phenyl in 4 by Cl- and I- was determined, and the stability sequence follows the normal trend seen in "soft" metal centers: i.e., the Pt has a preference for the halide in the order I > Cl > F; the difference is, however, fairly small. The substitution kinetics follow the usual two-term rate law, and the rate constants for the solvolytic (k1) and the direct (k2) reaction pathways were determined to be k1 = (9.7 ± 2.4) × 10-5 s-1, k2 = (11.7 ± 0.3) × 10-2 M-1 s-1 and k1 = (7.1 ± 4.9) × 10-5 s-1, k2 = (23.0 ± 1.3) × 10-2 M-1 s-1 for Cl- and I-, respectively. Activation parameters for the solvolytic and direct pathways with Cl- as incoming ligand are typical for associative processes and were determined to be H = 77.8 ± 5.5 kJ mol-1, S = -56 ± 18 J K-1mol-1 and H = 67.6 ± 1.8 kJ mol-1, S = -37 ± 6 J K-1mol-1, respectively. Complexes 4 and 5 react with Me3SnPh, and within 2-15 min there is a complete conversion to products. 4 gives a single product, trans-[PtPhMe(PPh3)2], which was characterized by X-ray crystallography. 5 gives two products: trans-[PtPhMe(PMe2Ph)2] and trans-[PtPh2(PMe2Ph)2]. Steric effects on the reactivity speak in favor of an associative mechanism. The surprisingly high reactivity for the transmetalations, compared to the substitution reactions, can be explained in terms of an associative mechanism, where a strong, bridging Sn-F interaction stabilizes the transition state. Furthermore, only trans products are formed; i.e., we have an exclusive F-for-R (R = Me, Ph) substitution at these platinum fluoro complexes. Treatment of 4 with phenylacetylene in benzene at room temperature gives the alkynyl complex trans-[PtPh(CCPh)(PPh3)2] (8).
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5.
  • Nilsson, S. L., et al. (författare)
  • Phosphate buffers in capillary electrophoresis/mass spectrometry using atmospheric pressure photo ionization and electrospray ionization
  • 2003
  • Ingår i: Rapid Communication in mass spectrometry. - : Wiley. - 0951-4198 .- 1097-0231. ; 17:20, s. 2267-2272
  • Tidskriftsartikel (refereegranskat)abstract
    • Capillary electrophoresis (CE) has been combined with atmospheric pressure photoionization (APPI) and electrospray ionization (ESI) for mass spectrometric (MS) detection. Separation conditions using potassium phosphate buffer and ammonium formate buffer have been compared for analysis of eleven pharmaceutical bases. The results showed improvements in separation efficiency and peak symmetry when phosphate buffer was used. The low flow in CE may enable utilization of these advances with MS detection. Compared with ESI, the APPI technique provided a cluster-free background. The enhanced signal-to-noise ratio in the total ion current (TIC) and the reduced spectral background indicated that the APPI process is less affected by non-volatile salts in the CE buffers. This results in a wider range of choice of CE buffers in CE/MS analysis when APPI is the ionization method.
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