We show how small- and wide-angle elastic light scattering (q similar to 0.03-30 mum(-1)) can be used to quantitatively characterize the structure of polymeric gels made of semi-flexible entangled fibers. We applied the technique to the study of fibrin gels grown from the polymerization of fibrinogen (FG) macromolecular monomers following activation by the enzyme thrombin (TH), at different concentrations and under different physical-chemical conditions of the gelling solution. Our findings show that the gel can be imagined as a random network of fibers of size d and density rho, entangled together to form densely packed blobs of mass fractal dimension D-m and average size xi, which may overlap by a factor eta and exhibit a long-range order. Provided that d greater than or equal to 50-100 nm, all of the above parameters can be recovered by the use of a global fitting function developed by us on the basis on the proposed gel model. When the fibers are thinner (d < similar to 50 nm), only the fiber mass/length ratio mu similar to rho d(2) can be retrieved instead of d and rho. Our data confirm and quantify the major changes in the gel structure that can be obtained by varying either the salt concentration of the solution and/or the molar ratio TH/FG. Gels formed in Tris-HCl 50 mM/NaCl 150 mM, pH 7.4 and TH/FG = 0.01 are characterized by relatively small, fairly branched (D-m similar to 1.4-2.0) fibers with a mass/length ratio independent of concentration. On reducing the TH/FG ratio, the fibers become increasingly thicker, with d similar to 90 nm at TH/FG = 10(-5). When the salt concentration is reduced to NaCl 100 mM (TH/FG = 0.01) the fibers are less branched (D-m similar to 1.2-1.4), but much thicker, with m increasing by an order of magnitude. These effects are quantitatively analyzed and discussed.
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Budapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, HungaryBudapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, Hungary
Hericz, D.
Sarkadi, T.
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Budapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, HungaryBudapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, Hungary
Sarkadi, T.
Erdei, G.
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Budapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, HungaryBudapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, Hungary
Erdei, G.
Lazuech, T.
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Budapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, Hungary
Polytech Paris Sud, Rue Joliot Curie, F-91190 Gif Sur Yvette, FranceBudapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, Hungary
Lazuech, T.
Lenk, S.
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Budapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, HungaryBudapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, Hungary
Lenk, S.
Koppa, P.
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Budapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, HungaryBudapest Univ Technol & Econ, Dept Atom Phys, Budafokiut 8, H-1111 Budapest, Hungary
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European Synchrotron Radiat Facil, ID15, F-38043 Grenoble, France
Univ New S Wales, Sch Mat Sci & Engn, Sydney, NSW, AustraliaEuropean Synchrotron Radiat Facil, ID15, F-38043 Grenoble, France
Daniels, J. E.
Pontoni, D.
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European Synchrotron Radiat Facil, ID15, F-38043 Grenoble, FranceEuropean Synchrotron Radiat Facil, ID15, F-38043 Grenoble, France
Pontoni, D.
Hoo, Rui Ping
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Univ New S Wales, Sch Mat Sci & Engn, Sydney, NSW, AustraliaEuropean Synchrotron Radiat Facil, ID15, F-38043 Grenoble, France
Hoo, Rui Ping
Honkimaeki, V.
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European Synchrotron Radiat Facil, ID15, F-38043 Grenoble, FranceEuropean Synchrotron Radiat Facil, ID15, F-38043 Grenoble, France