ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Articles  (281)
Collection
Journal
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 4327-4335 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 5001-5013 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 24 (1991), S. 6332-6334 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 6808-6818 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 17 (1984), S. 2928-2930 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 5459-5473 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The behavior of monomer density profiles of a star polymer in a d-dimensional good solvent, which was predicted in an earlier paper using scaling arguments, is now derived by using the renormalization group ε=4−d expansion method. Both the case of a free star in the bulk and of a center-adsorbed star at a free surface are considered. In the latter case of a semi-infinite problem, a distinction is made between repulsive walls, attractive walls—where for large arm length l, the configuration of the star is quasi-(d−1)-dimensional—and "marginal walls,'' where for l→∞ the transition from d-dimensional to (d−1)-dimensional structure occurs. For free stars, ρ(r) behaves as r−d+1/ν for small r, where ν is the exponent describing the linear dimensions of the star, e.g., the gyration radius Rgyr∼lν. For center-adsorbed stars at repulsive or marginal walls, ρ(r(parallel),z) behaves as ρ(r(parallel),0)∼r−d+λ( f )(parallel) and ρ(0,z)∼z−d+1/ν, where r(parallel) and z denote the distances parallel and perpendicular to the surface, respectively; the new exponent λ( f ) depends explicitly on the number of arms f in general. We calculate this exponent λ( f ) to first order in ε=4−d; then λ( f ) is obtained to be (f−1)ε/4+O(ε2) for repulsive walls and 2−ε/4+O(ε2) for marginal walls.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 8537-8541 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Wetting transitions of binary polymer mixtures in contact with a wall were studied using lattice models by the method of Monte Carlo simulation. First-order wetting transitions were found below the critical temperature but at a moderately high volume fraction of the polymer type favored by the wall. The transitions appear to be second order at low temperatures or for short chain lengths.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 7265-7275 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A theory is presented to describe the nucleation and subsequent growth of weakly inhomogeneous lamellar phases from a supercooled disordered phase. Detailed calculations are performed for the case of near-symmetric diblock copolymer melts, although the results have relevance for other physical systems in the Brazovskii "universality class.'' Nucleation phenomena in such systems are particularly interesting because the bulk phase transitions have a very weak, fluctuation-induced first order character. We find unusually small nucleation barriers and critically slowed growth kinetics. For a diblock copolymer melt with degree of polymerization N and undercooling δ∝(Tt−T)/Tt(very-much-less-than)1, the barrier is of order ΔF*/kBT∼N−1/3δ−2. Our estimate for the completion time of the nucleation and growth processes is θc ∼N1/12 δ−3/4 τd exp(ΔF*/4kBT), where τd is the copolymer terminal relaxation time.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 7602-7614 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We use molecular dynamics computer simulations to study the equilibrium properties of the surface of amorphous silica. Two types of geometries are investigated: (i) clusters with different diameters (13.5, 19, and 26.5 Å) and (ii) a thin film with thickness 29 Å. We find that the shape of the clusters is independent of temperature and that it becomes more spherical with increasing size. The surface energy is in qualitative agreement with the experimental value for the surface tension. The density distribution function shows a small peak just below the surface, the origin of which is traced back to a local chemical ordering at the surface. Close to the surface the partial radial distribution functions as well as the distributions of the bond–bond angles show features which are not observed in the interior of the systems. By calculating the distribution of the length of the Si–O rings we can show that these additional features are related to the presence of two-membered rings at the surface. The surface density of these structures is around 0.6/nm2, in good agreement with experimental estimates. From the behavior of the mean-squared displacement at low temperatures, we conclude that at the surface the cage of the particles is larger than the one in the bulk. Close to the surface the diffusion constant is somewhat larger than the one in the bulk and with decreasing temperature the relative difference grows. The total vibrational density of states at the surface is similar to the one in the bulk. However, if only the one for the silicon atoms is considered, significant differences are found. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 9288-9299 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The bond fluctuation model of polymer chains on lattices is used to study layers of polymers anchored with one end at a hard wall, assuming good solvent conditions and repulsive interactions between the monomers and the wall. Chain lengths from N=10 to N=80 and grafting densities σ from 0.025 to 0.20 are considered, both for the "quenched'' case, where the anchor points are kept fixed at randomly chosen surface sites, and the "annealed'' case, where lateral diffusion of the anchored ends at the wall is considered. Profiles of monomer density and free end density, chain linear dimensions parallel and perpendicular to the wall, as well as corresponding mean square displacements of inner and end monomers are studied and discussed in the light of current theoretical predictions, and it is shown that most of these properties can be understood in terms of appropriate scaling concepts. Both the relaxation of the total chain configurations and the time dependence of monomer mean square displacements are studied. In the annealed case the lateral diffusion constant D is found to behave as D∼σ−qN−p, where q=2/3 and p crosses over from p≈1 at small σ to p≈2 at large σ. The results for the relaxation time τ are consistent with the recent scaling prediction τ∼σbNa with a=3 and b=2/3.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...