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51.
Chargeability of ethanol–petrol biofuels during refuelling has been studied in real dispenser environment in order to assess safety risks due to fuel charging at fuel filling stations. Two biofuel blends were studied: E10 containing 10 vol-% of ethanol and 90 vol-% of petrol, and E85 containing about 85 vol-% of ethanol and 15 vol-% of petrol. Charging of standard 95 Octane petrol was studied as a reference. The results show that the charging of E85 is negligible and no charge will be accumulated as long as the fuel dispenser system is properly grounded. In the case of refuelling with E10, charge is accumulated but the level of total charge is still so low that no real electrostatic ignition hazards exist due to fuel charging at filling stations as long as the system is properly grounded. Electrostatic ignition hazards due to fuel charging are real only for standard petrol fuel. 相似文献
52.
Arja Sarpola Vesa Hietapelto Jorma Jalonen Jukka Jokela Risto S. Laitinen Jaakko Rämö 《Journal of mass spectrometry : JMS》2004,39(10):1209-1218
Earlier characterization of some hydrolysis products of AlCl3·6H2O was confirmed by electrospray ionization tandem mass spectrometry with increasing collision energy of projectile ions. At lower collision energies, the aqua ligands were stripped off. At higher energies, two hydroxo groups formed a bridging oxo group with loss of one water molecule. Aluminum complexes could also capture aqua ligands in the collision chamber so long as the parent ion did not fragment, and the fragment ion spectra broadened toward higher m/z values. The chloro ligands were eliminated as hydrochloric acid. The aluminum cores remained highly intact. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
53.
Jaakko Paasivirta Harri Hkli Karl-Gustav Widen 《Magnetic resonance in chemistry : MRC》1974,6(7):380-383
Structure proof of (—)-myrtenol, 3-cyclopentenyl-1-methanol and 5-norbornene-2-endo-methanol has been obtained from their proton magnetic resonance spectra in carbon tetrachloride containing different added amounts of tris(dipivaloylmethanato)europium. For each alcohol, a 1:1 complex structure with Eu(dpm)3 could be computed, in which the calculated pseudocontact shift effects on all skeleton protons of the ring system were consistent with the observed shift effect values. A considerable contact contribution of opposite sign to that of the pseudocontact part of the effect could be estimated for the methylene protons of the CH2OH group. 相似文献
54.
55.
Hellman H Laitinen RS Kaila L Jalonen J Hietapelto V Jokela J Sarpola A Rämö J 《Journal of mass spectrometry : JMS》2006,41(11):1421-1429
The hydrolysis reactions of FeCl3 in 0.1 mM aqueous solutions were monitored by electrospray ionisation time-of-flight mass spectrometry (ESI-ToF-MS). In contrast to the other ionisation techniques, electrospray ionisation provides information on the composition of the elemental cores even in water and salt cluster ions. Therefore, the technique facilitates detection of the bonding of the chloride ions in the oxo-hydroxo-iron cores. A variety of mononuclear and polynuclear iron-oxohydroxo-chloride complexes were characterised from the cationic and anionic mass spectra of iron(III) solutions. Oxidation and reduction reactions of iron, as well as competition between OH- and Cl- ions within one iron core, were also observed. 相似文献
56.
Pauliina Ilmonen Jaakko Nevalainen Hannu Oja 《Statistics & probability letters》2010,80(23-24):1844-1853
We consider a semiparametric multivariate location–scatter model where the standardized random vector of the model is fixed using simultaneously two location vectors and two scatter matrices. The approach using location and scatter functionals based on the first four moments serves as our main example. The four functionals yield in a natural way the corresponding skewness, kurtosis and unmixing matrix functionals. Affine transformation based on the unmixing matrix transforms the variable to an invariant coordinate system. The limiting properties of the skewness, kurtosis, and unmixing matrix estimates are derived under general conditions. We discuss related statistical inference problems, the role of the sample statistics in testing for normality and ellipticity, and connections to invariant coordinate selection and independent component analysis. 相似文献
57.
Takhistov VV Khoroshko LO Viktorovskii IV Lahtiperä M Paasivirta J 《European journal of mass spectrometry (Chichester, England)》2004,10(5):737-741
Nine polysulfides, previously unknown as environmental organic pollutants, were analyzed from a sediment sample from the Eastern Gulf of Finland. The determinations were done by gas chromatography connected to low- and high-resolution mass spectrometers. The structure of the polysulfides was elucidated by determination of isotopic composition of abundant molecular and fragment ions by high-resolution mass spectrometry (HRMS), the interpretation of ion structures in low-resolution mass spectra (LMRS) using the thermochemical approach, the application of fragmentation rules and performing the ICLU simulation of abundance of ions in isotope clusters. Seven compounds were known in literature, but mass spectra were reported for only two of them, both recorded from mixture. Struture evaluation was successful for other substances, but not for the substance(s) in first eluting GC peak, where HRMS date were not obtained. Suggested structures of the cyclic compounds were (in the order of GC retention) 3,4-dithiacyclohexene, 1,2,3-trithiacyclohexane, 3,4,5- trithiacyclohexene, 1,2,4-trithiacyclohexane, cyclopropyl hydrodisulfide, 1,2-dithiole-3-thione and 1,2,3,4,5-penta- thiacyclo-octane. One acyclic congener identified was dimethyl tetrasulfide. 相似文献
58.
Jaakko T. Astola 《Discrete Applied Mathematics》1984,7(1):17-21
It is shown that an analog of the Tietäväinen bound for binary codes holds also for spherical codes. 相似文献
59.
Sarpola AT Saukkoriipi JJ Hietapelto VK Jalonen JE Jokela JT Joensuu PH Laasonen KE Rämö JH 《Physical chemistry chemical physics : PCCP》2007,9(3):377-388
ElectroSpray Ionization-Mass Spectrometry (ESI-MS) and computational methods (DFT, MP2, and COSMO) were used to investigate the hydrolysis products of aluminium chloride as a function of sulfate concentration at pH 3.7. With the aid of computational chemistry, structural information was deduced from the chemical compositions observed with ESI-MS. Many novel types of hydrolysis products were noted, revealing that our present understanding of aluminium speciation is too simple. The role of counterions was found to be critical: the speciation of aluminium changed markedly as a function of sulfate concentration. Ab initio calculations were used to reveal the energetically most favoured structures of aluminium sulfate anions and cations selected from the ESI-MS results. Several interesting observations were made. Most importantly, the bonding behaviour of the sulfate group changed as the number of aqua ligands increased. The accompanying structural rearrangement of the clusters revealed the highly active role of sulfate as a ligand. The gas phase calculations were expanded to the aquatic environment using a conductor-like screening model. As expected, the bonding behaviour of the sulfate group in the minimum energy structures was distinctly different in the aquatic environment compared to the gas phase. Together, these methods open a new window for research in the solution chemistry of aluminium species. 相似文献
60.
Dr. Shaochen Zhou Lotta Gustavsson Dr. Grégory Beaune Dr. Sourov Chandra Prof. Jukka Niskanen Prof. Janne Ruokolainen Dr. Jaakko V. I. Timonen Prof. Olli Ikkala Dr. Bo Peng Prof. Robin H. A. Ras 《Angewandte Chemie (International ed. in English)》2023,62(49):e202312679
Near-infrared (NIR) fluorophores with pH-responsive properties suggest merits in biological analyses. This work establishes a general and effective method to obtain pH-responsive NIR emissive gold nanoclusters by introducing aliphatic tertiary amine (TA) groups into the ligands. Computational study suggests that the pH-responsive NIR emission is associated with electronic structure change upon protonation and deprotonation of TA groups. Photo-induced electron transfer between deprotonated TA groups and the surface Au-S motifs of gold nanoclusters can disrupt the radiative transitions and thereby decrease the photoluminescence intensity in basic environments (pH=7–11). By contrast, protonated TA groups curb the electron transfer and restore the photoluminescence intensity in acidic environments (pH=4–7). The pH-responsive NIR-emitting gold nanoclusters serve as a specific and sensitive probe for the lysosomes in the cells, offering non-invasive emissions without interferences from intracellular autofluorescence. 相似文献