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  • Polymer and Materials Science  (11)
  • 25.85.−w  (1)
  • Electrocardiogram  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Psychopharmacology 102 (1990), S. 379-382 
    ISSN: 1432-2072
    Schlagwort(e): Paroxetine ; Amitriptyline ; Electrocardiogram ; Blood pressure ; Systolic time intervals ; Plasma drug concentration
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract In a double-blind clinical study, electrocardiogram, blood pressure and systolic time intervals were measured in 40 depressive patients treated with either paroxetine (30 mg/day) or amitriptyline (150 mg/day) for 6 weeks. While amitriptyline significantly increased the heart rate, the QTc interval and the PEP/LVET ratio, paroxetine did not alter any of the cardiovascular parameters measured.
    Materialart: Digitale Medien
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  • 2
    ISSN: 1434-601X
    Schlagwort(e): 25.70.Lm ; 25.85.−w
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Events with 2, 3 and 4 heavy fragments (A≥20) detected in the reactions100Mo +100Mo at 18.7, 23.7 A·MeV and120Sn +120Sn at 18.4 A·MeV were analyzed by means of an improved version of the kinematic coincidence method. The phase-space distributions prove that 3- (and possibly 4-) body events predominantly originate from a two-step mechanism and are compatible with the hypothesis of a binary deep-inelastic interaction followed by the further fissionlike decay of one (or both) of the primary fragments. The characteristics of the fission step — mass asymmetry, relative velocity, in-plane and out-of-plane angles — have been reconstructed for the 3-body events and indications are found that nonequilibrium effects at the end of the deep-inelastic phase may influence the fissionlike decay.
    Materialart: Digitale Medien
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  • 3
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: If a polymer molecule is solved within a polymer melt of the same chemical nature but of different molecular weight, the solved polymer molecule in general is expanded as compared with the unperturbed statistical coil. The expansion coefficient and the second osmotic virial coefficient depend on the molecular weights of both polymers. The experimental results follow the lattice theory for athermic solutions of polymers.
    Notizen: Wird ein Polymermolekül in einer Polymerschmelze von gleicher chemischer Art aber anderem Molekulargewicht gelöst, so ist das gelöste Polymermolekül im allgemeinen relativ zum ungestörten statistischen Knäuel expandiert. Der Expansionskoeffizient und der zweite osmotische Virialkoeffizient hängen von den Molekulargewichten der beiden Polymeren ab. Die experimentellen Befunde werden durch die Gittertheorie für athermische Lösungen von Polymeren richtig beschrieben.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 4
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: With the aid of small-angle neutron scattering the molecularly disperse character of a clear mixture of two polymers in the absence of a low molecular weight compound is proved in one case and disproved in the other. If the mixture is molecularly disperse the chemical potential and the coil dimensions can be determined. Poly(methyl methacrylate) and styrene-acrylonitrile copolymers for certain compositions of the copolymer form molecularly disperse mixtures. They are exothermic, have a negative excess entropy of mixing and the coils are expanded as compared with the unperturbed coil dimensions. The theory of solubility parameters of Hildebrand and Scott enables one to find the miscible system, but the experimental second osmotic virial coefficients differ by an order of magnitude from those which could be estimated from this theory.
    Notizen: Mit Hilfe der Neutronenkleinwinkelstreuung wird der molekulardisperse Charakter einer glasklaren Mischung von zwei Polymeren bei Abwesenheit eines niedermolekularen Lösungsmittels in einem Fall nachgewiesen, im anderen widerlegt. Falls eine molekulardisperse Mischung vorliegt, können das chemische Potential und die Knäueldimensionen bestimmt werden. Polymethylmethacrylat und Styrol-Acrylnitril-Copolymere bilden für gewisse Zusammensetzungen des Copolymeren molekulardisperse Mischungen. Sie sind exotherm, besitzen eine negative Exzeßentropie und die Molekülknäuel sind gegenüber den ungestörten Knäueldimensionen expandiert. Die Theorie der Löslichkeitsparameter von Hildebrand und Scott ermöglichte zwar die Auffindung des mischbaren Systems, aber die gemessenen zweiten osmotischen Virialkoeffizienten sind in der Größenordnung verschieden von denen, die nach dieser Theorie vorausberechnet werden können.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 5
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Provided a polymer is soluble, i. e., molecularly dispersed in another polymer irrespective of the molecular weight of the components, the solution is exothermic. By increasing the temperature two effects, both unfavourable to mixing become larger: (i) the excess entropy of mixing caused by contact interaction and (ii) the total effect from the difference of the free volumes of the pure components. So, an upper miscibility gap occurs. The thermodynamic properties of the mixture cannot be derived from the properties of the pure components. They can be described by the corresponding states theory of Prigogine, Flory, and Patterson with suitable values for the contact energy and contact entropy parameters X12 and Q12. The temperature of separation can be predicted from measurements on the mixture at low temperatures.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
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  • 6
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Light scattering, neutron scattering and viscosity measurements on a nematic and a smectic polymethacrylate demonstrate the presence of molecularly disperse coils in solution. For the nematic polymer, toluene is a theta solvent, the behaviour familiar from conventional polymers (unperturbed coil conformation) being exhibited at the theta point. The isotropic melts likewise contain unperturbed coils; in the case of the nematic polymers, however, the coils in the melt have a radius of gyration which is about 30% smaller than that in solution at the theta point. In the liquid-crystalline phase, the mean radii of gyration in both cases are identical to the corresponding parameters in the isotropic melt. In the nematic material, however, the coils can be shown to have a substantial anisotropy, the radius of gyration parallel to the director being about 20% smaller than that at right angles to this direction. On the basis of a theoretical chain simulation, a model for the main-chain conformation has been developed which takes into account both short-range interactions along the main chains and three-dimensional interactions by the oriented side groups. This model indicates the degree of orientation from which a change in the mean radius of gyration can be expected. Wide-angle neutron scattering experiments on smectic polymer provide information about the main-chain distribution in the smectic phase. The main chains are present in a substantially higher concentration between the smectic layers, but there are hints that they do not have a true two-dimensional arrangement.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 178 (1977), S. 1793-1810 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: An improved anionic polymerization technique for the preparation of highly uniform styrene/α-methylstyrene linear two-block copolymers is described. Three sets of samples with molecular weights M were prepared under equal experimental conditions, namely polystyrenes (2 · 105 〈 M 〈 3 · 106), poly(α-methylstyrene)s (7 · 104 〈 M 〈 4 · 106), and block copolymers (2 · 105 〈 M 〈 2,5 · 106). Ultracentrifugation in a density-gradient does not show any chemical heterogeneities in the block copolymers. The molecular polydispersity U = Mw/Mn-1 is U = 0,03 or less as estimated from GPC-measurements. The high molecular and chemical homogeneity of the block copolymers and the optical similarity of the two segment types yield light scattering measurements which give molecular weights Mw, radii of gyration 〈r2〉1/2 and second virial coefficients A2 with almost the same accuracy as in the case of homopolymers. The radii of gyration and the intrinsic viscosities of the block copolymers give no evidence for any “intramolecular phase separation” in the good solvent toluene. The coil conformation corresponds closely to that of the homopolymers.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 8
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The structure and the thermodynamics of polymer blends made from two poly(styrene/acrylonitrile) copolymers with a different ratio of styrene/acrylonitrile are investigated by neutron scattering. These systems are endothermic, exhibit a positive value for the Huggins parameter χ and show phase separation at sufficiently large molecular weights. The results are in good agreement with the corresponding states theory of Prigogine and Patterson. Other polymer blends are exothermic, exhibit negative χ-values and are compatible even for infinitely large molecular weights. In these cases one can adapt the theoretical equations to the experiments by the introduction of a suitable parameter for an exothermic contact energy. This is shown for blends from poly(methyl methacrylate) and poly(styrene/acrylonitrile).
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 9
    ISSN: 1022-1352
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: An iterative, approximative procedure is presented, to calibrate the determination of molar masses of polymers with gel-permeation chromatography, additionally using viscometry, and transformations, according to Benoit's concept of universal calibration, even if only polymers with broad molar mass distribution are available. The calculated (intermediate) values of the average molar masses from each step of iteration converge to final values. With at least two fractions of the polymers to be analyzed, and with measured intrinsic viscosities of the fractions, a calibration curve of gel-permeation chromatography and Mark-Houwink's constants can be determined. Assumptions for the use of the calibration procedure are the existence of linear calibration curves for gel-permeation chromatography, constant Mark-Houwink's exponents, and a common universal calibration curve according to Benoit, of the polymers of interest, and of another polymer for comparison. From this second polymer the Mark-Houwink equation must be known (or measurable with acceptable expense), and sufficient uniform fractions for chromatography must be available. In aqueous saline the assumptions are fulfilled by hyperpolymers of human haemoglobin, and by native proteins, as shown in a previous paper. The new procedure was applied to fractions of those hyperpolymers, it was evaluated, and variants of the procedure were compared. The evaluation was done by comparison of the number-and mass-averages of the molar masses of the fractions of haemoglobin hyperpolymers, determined with gel-permeation chromatography calibrated with the new procedure, with the values obtained from osmometry and light scattering. The goodness of the new procedure, especially the power of correction of molar masses, can be demonstrated with the application to fractions of haemoglobin hyperpolymers, it changes with their uniformity. Furthermore, the new procedure shows its efficiency, when three steps of iteration are enough to reach the final values. At last, with a Benoit transformation of the averages of molar masses, obtained by a theoretical consideration within the given marginal conditions, a rectification of the new procedure is given.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 16 (1995), S. 771-778 
    ISSN: 1022-1336
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Amorphous blends from a deuterated polyaryletherketone and a polyetherimide have been prepared and investigated by neutron scattering. The used components differ remarkably in their structure and their solution properties. The blends on the other hand are combinatorial mixtures: the scattering quantity φ1φ2/S(q) is independent of the composition of the blends if the polymer chains have the same length.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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