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  • Wiley-Blackwell  (7)
  • Springer  (1)
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  • 1
    ISSN: 1573-7357
    Keywords: 74.20.−z ; 74.65.+n ; 74.60.Mj
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The thermodynamics of the Coulomb Bose-gas (CBG) is studied using the Bogoliubov approximation. Within this approximation the condensate density did not tend to zero as the transition temperature, Tc, was approached, but remained finite, resulting in a first order phase transition. By the use of the condensate density as the only temperature dependent feature of the electromagnetic screening the London penetration depth is derived. The free energy of the system and the specific heat are calculated. We report a well defined λ-point transition in the specific heat. Comparisons are made with the experimental results for YBCO, a high temperature superconductor. We also report recient findings of the Bose-Einstein condensation of CBG in a magnetic field at ultra-low temperatures and ultra-high magnetic fields. A low-temperature dependence of the upper critical field Hc2(T) is obtained both for the particle-impurity and particle-particle scattering.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 1057-1062 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The competitive binding of fluorescence-tagged poly(methacrylate) polyanions and poly(phosphate) polyanions with different poly(N-alkyl-4-vinylpyridinium) polycation quenchers (alkyl = methyl, ethyl and propyl) was studied in the region 278÷333 K by fluorescence quenching technique. The equilibrium of this interpolyelectrolyte substitution reaction proved to be temperature sensitive except in the case when the poly(N-methyl-4-vinylpyridinium) polycation was used. Thermodynamic parameters of the reaction were determined. The possibility of effective temperature control of the interpolyelectrolyte reaction might be important for understanding, prediction and utilization of transformation processes of complex particles formed by electrostatically complementary (biological) macromolecules.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 2 (1981), S. 343-346 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 4
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Interpolymer reactions between poly(acrylic acid) (PAA) or poly(methacrylic acid) (PMAA) and poly(N-tert-butylaziridine) (PTBA) were studied and compared with the corresponding reactions of these polyacids with linear polyethyleneimine (LPEI). In aqueous alkaline and salt media the presence of the bulky non-polar N-substituent in the main chain of PTBA results in a decrease of stability of polyacid-PTBA polyelectrolyte complexes. LPEI, which forms stronger salt bonds with PAA, substitutes PTBA in the PAA-PTBA polyelectrolyte complexes. Addition of simple salts to aqueous solutions of non-stoichiometric polyelectrolyte complexes (N-PEC) PAA-PTBA and PMAA-PTBA at room temperature causes a phase separation due to macromolecular exchange and disproportionation reactions. At elevated temperatures (T = 40 - 60 °C), however, the macromolecular exchange between different N-PEC particles does not occur and phase separation in aqueous salt solution of the N-PEC's PAA-PTBA, PMAA-PTBA is not observed. This is attributed to hydrophobic interactions in polyacid-PTBA complexes due to the presence of the tert-butyl groups in the latter.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 191 (1990), S. 2801-2814 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Being solubilized in systems of reversed micelles of a surfactant, the macromolecules incorporate into the inner cavities of the micelles, whose size can be changed by varying the degree of hydration, w0 = [H2O]/[surfactant]. The conjugates of proteins (α-chymotrypsin, bovine serum albumin (BSA), monoclonal antibodies to insulin) with linear polyelectrolytes (poly(methacrylic acid), quaternized poly(4-vinylpyridine)) are synthesized in reversed micelles of Aerosol OT (sodium bis(2-ethylhexyl)sulfosuccinate) in the octane with 100% yield. The yield critically depends on the degree of hydration: the reaction does not proceed at low w0, but if w0 exceeds a threshold value (which differs for various macromolecules) the yield increases sharply and reaches 100%. Using the ultracentrifugation it was demonstrated that at low w0 the polyelectrolyte represents a compact globule compressed by the micellar matrix in the inner cavity of a micelle. Under these conditions, there is no space for the protein in a micelle which contains polyelectrolyte, and therefore reaction does not proceed. If w0 exceeds a threshold value the micelles become large enough to entrap the conjugated macromolecules simultaneously. The possibility of regulation of the conjugate composition by variation of w0 (via the size of the micellar matrix) was demonstrated by a conjugate of BSA with quaternized poly(4-vinylpyridine).
    Additional Material: 7 Ill.
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  • 7
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A tool was developed for enhancement of plasmid penetration into an intact cell, based on increasing DNA hydrophobicity via inclusion into a soluble interpolyelectrolyte complex (IPC) with polycations. The characteristics of formation of DNA IPC with synthetic polycations [poly(N-ethyl-4-vinylpyridinium)bromide (PVP) and PVP modified with 3% of N-cetyl-4-vinylpyridinium units (PVP-C)] were studied using ultracentrifugation and polyacrylamide gel electrophoresis methods. The conditions were established under which the mixing of DNA and polycation aqueous solutions results in the selfassembly of soluble IPC species. Incorporation of DNA into IPC results in the enhancement of DNA binding with isolated Bacillus subtilis membranes. A considerable increase in the efficiency of transformation of B. subtilis cells with pBC16 plasmid resulted from incorporation of the plasmid into the IPC with PVP and CVP.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 2211-2216 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The interaction between oppositely charged linear and crosslinked polyelectrolytes and the molecular mechanism of the transport of linear polyelectrolytes into oppositely charged gels were studied. The mechanism represents a “relay-race” transfer of polyion segments from one fragment of the polyelectrolyte network to the other via interpolyelectrolyte exchange reaction. Thus, the whole layer of the formed interpolyelectrolyte complex serves as an active zone. The driving force for the transport is produced by interpolyelectrolyte addition reaction on the solution/gel interface.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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