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  • 1
    ISSN: 1434-601X
    Keywords: 24.60.Dr ; 24.60.Gv ; 25.80.Ls
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The previously published INDEX model is tested for nucleon spectra fromp- andα-induced reactions. The results of two alternative versions, the INCLUSIVE INDEX model and the EXCLUSIVE INDEX model, quite well agree with the data. It is found that in the INCLUSIVE INDEX model three preequilibrium stages are sufficient to describe single- and multi-nucleon emission. The model provides an useful first order estimate of the influence of the finite Fermi energy on particle spectra. This effect is very strong for nucleon induced reactions while forα-induced reactions it can be neglected. The deduced mean-free-path multiplier corroborates the long stated discrepancy between models in which excitons interact independently or not. Using preequilibrium parameters similar to those found for nucleon induced reactions the important branching ratio of contributingnp andpp pairs in stoppedπ −-absorption can be determined by INDEX model calculations. Deduced values from publishedn- andp-spectra agree reasonably well with those of other experimental analyses but deviate significantly from microscopic model predictions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 328 (1987), S. 333-350 
    ISSN: 1434-601X
    Keywords: 24.60.Dr ; 24.60.Gv
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Starting from a previous ansatz ofindependently interacting excitons the more refined model INCLUSIVE INDEX is developed yieldinginclusive preequilibrium proton and neutron spectra. It is shown that three stages are sufficient to describe single- and multi-nucleon emission to all orders of practical importance. By use of recurrence relations the loss of particles and energy due to emission from previous stages is fully accounted for. In order to predict the population of specific residual nuclei the precompound process is reformulated in terms ofexclusive emission spectra. This intricate statistical problem is solved in the EXCLUSIVE INDEX model by algorithms representing the average probability for a specified number of particles not to be emitted but to reach the next stage of nuclear relaxation. Differential excitation probabilities can be calculated for those six nuclei which are populated by the emission of none, one, or two preequilibrium nucleons in two stages via alltogether 15 principal paths. Typical features of the INCLUSIVE and EXCLUSIVE INDEX model are discussed. The strength of one- and two-nucleon emission is compared with HYBRID model predictions.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 333 (1989), S. 45-56 
    ISSN: 1434-601X
    Keywords: 24.60.Dr ; 24.60.Gv ; 25.40.−h ; 25.45.−z ; 25.55.−e ; 25.70.Gh
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The previously introduced EXCLUSIVE INDEX model allows to predict the population of 6 residual nuclei including the primary compound nucleus through two stages of the preequilibrium phase. The present version is limited to maximum two-nucleon emission. The preequilibrium ejectiles may reduce the brought-in rotational energy by a model of maximum angular momentum decoupling. Subsequent evaporation of protons, neutrons andα-particles is treated in the frame of the Weisskopf-Ewing ands-wave approximation considering pairing effects only in compound nucleus state densities. The sensitivity of essential preequilibrium parameters on the shape of calculated excitation functions is tested. The model predictions well compare to excitation functions fromp, d,3He and4He induced reactions including the large set from the reaction93Nb(4He,xn yp) up to 170 MeV bombarding energy. The general importance of two-nucleon preequilibrium emission is accentuated in several examples. The deduced preequilibrium parameters corroborate the results from the INDEX model analysis of nucleon spectra.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0947-3440
    Keywords: Thermotropic and lyotropic phase behavior ; Amphotropes ; Surfactants ; Liquid crystals ; Chromophores ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New ammonium amphiphiles having a N,N-dimethyl-N-hydroxyethylammonium headgroup and various azobenzene mesogenic units connected by a decyl or dodecyl spacer have been synthesized. The azobenzene unit is functionalized at the 4-position with a cyano, methoxy or fluoro substituent. For the cyano-substituted amphotropes and the fluoro compound with a dodecyl spacer a smectic phase is formed as was observed by differential scanning calorimetry and polarization microscopy. Complexation with sodium dodecyl sulfate, SDS, in a 1:1 molar ratio induces the formation of a smectic phase for the compounds with a decyl spacer. The compounds with a dodecyl spacer showed rather complex behavior attributed to different crystal morphologies. The ammonium amphotropes form aggregates in water when heated above their Krafft temperature. However, these aggregates are not stable and crystallize upon cooling. The ion pair amphiphiles with SDS as second component form vesicles in water as observed by optical and electron microscopy. The observed blue shift in the UV absorption maximum of the amphotropes upon addition of SDS indicates π-π stacking between mesogenic units resulting from aggregation.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1434-193X
    Keywords: UV spectroscopy ; Poly(maleic acid-co-alkyl vinyl ether)s ; Azobenzene ; (Cyanobiphenylyl)oxy ; Cooperative binding ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -The interaction of poly(maleic acid-co-alkyl vinyl ether)s and poly(sulfonylethyl maleic acid monoamide-co-alkyl vinyl ether)s with and without (cyanobiphenylyl)oxy chromophores with N-[ω-(substituted azobenzoxy)alkyl]-N,N-dimethyl-N-hydroxyethylammonium bromide surfactants has been studied by UV spectroscopy. The azobenzene unit is functionalized at the 4′-position with a cyano or fluoro substituent and is connected to the surfactant headgroup via a decyl or dodecyl spacer. Upon addition of surfactants to poly(maleic acid-co-butyl vinyl ether) the absorption maxima (λmax) of the azobenzene chromophores immediately show their maximum blue shift. This indicates cooperative binding of surfactant to this polymer, and the formation of micelle-like aggregates surrounded by polyelectrolyte is assumed. Upon addition of the surfactants to the other polyelectrolytes λmax values of the azobenzoxy chromophores gradually shift to lower values indicating a lower cooperativity of surfactant binding. This is attributed to the formation of microdomains by the polyelectrolytes themselves. For these systems the formation of mixed micelles is assumed. The compactness of the microdomains of the maleic acid copolymers is influenced by the pH and binding with surfactants is also influenced by pH. The sulfonylethyl maleic acid monoamide copolymers show no pH dependence in binding above neutral pH. For these polyelectrolytes the cooperativity also becomes less with a longer spacer between backbone and chromophore. Upon elongation of the surfactant spacer or changing the end group from a cyano to the more hydrophobic fluoro substituent a lower λmaxis observed for the chromophores upon initial binding to the polyelectrolytes indicating more cooperative binding. When surfactants and polyelectrolytes are both labelled with chromophores, binding proceeds noncooperatively and the formation of mixed micelles is assumed.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1434-193X
    Keywords: Surfactants ; H aggregates ; Ion pairs ; Copper(II) binding ; Copper ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -A novel, single-chained ammonium amphiphile that carries an o-hydroxyazobenzene unit at the terminus of its hydrophobic chain has been synthesized. This compound forms ordered thread-like aggregates upon dispersion in water. These aggregates exhibit a phase transition at 56 °C. The o-hydroxyazobenzene unit binds several transition-metal ions in a 2:1 stoichiometry. Binding of these metal ions results in a lowering of the critical aggregation concentration. From the changes in the UV absorption spectrum it is concluded that the Cu2+ complex forms more tightly packed aggregates in water than the Zn2+ and Ni2+ complexes.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new series of rigid polymers was synthesized via radical copolymerization of N-phenylmaleimides, bearing pendant chromophores, with 4-vinylpyridine or styrene. Structural characterization was achieved by 1H NMR and 13C NMR spectroscopy, gel permeation chromatography (GPC), elemental analysis and differential scanning calorimetry (DSC). The thermal properties as well as the morphology of the investigated polymers at the air-water interface appear to be related to their rigidity. In spite of the presence of excellent mesogenic units, the polymers do not exhibit liquid crystalline behaviour. The 4-vinylpyridine copolymers form stable monolayers at the air-water interface. The attached chromophores electronically behave as monomers, as shown with in situ UVVIS absorption spectroscopy. Brewster angle microscopy shows a spontaneous aggregation of these polymers into domains on a neutral subphase, whereas on an acidic subphase a more homogeneous monolayer is formed. The monolayers give Z-type transfer onto hydrophilic quartz. However, the chromophores seem to be oriented randomly at the substrate surface. The styrene copolymers do not form stable monolayers as a result of crystallization at the air-water interface.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 1449-1454 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A computer program has been devised for routine use which processes raw data such as polymer sample weight, moisture content, solution volume, and viscometer flow times to calculate a least-squares-derived intrinsic viscosity. In addition to eliminating errors inherent in graphic solutions and freeing technicians from tedious calculation, the computer output provides the 95% confidence interval of the intrinsic viscosity.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0935-9648
    Keywords: Sensors ; ISFETs and CHEMFETs ; Polysiloxanes ; Reference FETs ; Polymer Membranes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Synthetic receptor molecules that selectively bind charged guests can store chemical information. The transduction of this information into electronic signals connects the chemical and electronic domains. Field effect transistors (FETs) are attractive transducing elements because these microdevices are able to register and amplify chemical changes at the gate oxide surface of the semiconductor chip.Integration of molecular receptors and field effect transistors into one chemical system gives a device that can communicate-changes of substrate activities in aqueous solution. Simulations of a system in which the receptor molecules are directly attached to the FET gate oxide indicate serious limitations with respect to sensitivity, dynamic range and extreme requirements for complex stability. Therefore we have concentrated on the integration of covalently attached thin membranes.The problem of the thermodynamically ill-defined oxidemembrane ipterface has been solved by applying a covalently linked hydrophilic polyhydroxyethylmethacrylate (polyHEMA) gel between the sensing membrane and the silylated gate oxide. A buffered aqueous electrolyte solution in the hydrogel renders the surface potential at the gate oxide constant via the dissociation equilibrium of the residual silanol groups. The subsequent attachment of a polysiloxane membrane that has the required dielectric constant, glass transition temperature Tg, and receptor molecule, provides a stable chemical system that transduces the complexation of cationic species into electronic signals (CHEMFET).The response to changing K⊕ concentrations in a solution of 0.1 M NaCl is fast (〈1 sec) and linear in the concentration range of 10-5-1.0 M (55-58 mV /decade). A reference FET (REFET) based on the same technology is obtained when the intrinsic sensitivity to changes in ion concentration is eliminated by the addition of 2.10-5 mol g-1 of didodecyldimethyl ammonium bromide to the ACE membrane. Differential measurements with a REFET/CHEMFET combination showed excellent linear K⊕ response over long periods of time.All chemical reactions used are compatible with planar IC technology and allow fabrication on wafer scale.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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