Biomedical subjects

Gert Frens

Publications and source records attributed to Gert Frens.

4 recordsLinked to original sources

PubMed2006

Indications for a surface temperature excess in heterogeneous catalysis.

We explored the surface temperature excess DeltaT = T(r) - T(m) (real reaction temperature T(r), measured catalyst temperature T(m)) on the basis of experimental data, a gradually curved Arrhenius plot for CO oxidation reactions over Pd/gamma-Al(2)O(3) catalysts. Such a plot could be an indication of the surface temperature excess in the 2-dimensional reaction surfaces of catalysts. The positive or negative surface temperature excess could be developed to be a general explanation for a gradually curved Arrhenius plot of a gas-solid catalytic system. This is a new insight into solving the puzzle on such common phenomena in heterogeneous catalysis. By using the reciprocal of the real reaction temperature T(r) in the hypothetical 2-D reaction surface, instead of the experimentally determined catalyst temperature T(m) or the gas temperature T(g), the gradually curved Arrhenius plot becomes linear. We investigated the implications of such a difference among T(r), T(m), and T(g). The surface temperature excess could be the effect of coupling between the fluxes of a chemical reaction and heat transport in the 2-D reaction surface. Its order of magnitude is 10 K for the present model system.(1) The surface temperature excess increases exponentially with the reaction temperature.

Journal Article↗

PubMed2005

Coil dimensions of the mussel adhesive protein Mefp-1.

To obtain a better understanding of factors controlling cross-linking rates of Mussel adhesive proteins, we study the conformation of the Mussel Adhesive Protein Mefp-1. The dimensions of Mefp-1 in solution are determined by dynamic light scattering. Under physiological conditions, the hydrodynamic radius RH of Mefp-1 is found to be 10.5+/-1.1 nm. Measured Mefp-1 dimensions are compared with theoretical dimensions of Mefp-1 in random coil conformations. We have strong indications that Mefp-1, under dilute and physiological conditions, has a self-avoiding random walk conformation with helix-like deca-peptide segments. With a number of segments of approximately 90, the segment length is found to be 2.7 nm.

Animals↗

PubMed2001

Marangoni Flow Driven Instabilities and Marginal Regeneration.

Fingering instabilities in films moving along wetted surfaces, dimpling in horizontal liquid films, and the drainage of vertical soap films by marginal regeneration are caused by surface tension gradients along the perimeter of the thin film. These gradients lead to a mechanical instability which involves Marangoni type liquid flow. It is possible to describe the conditions for the onset of marginal regeneration with a critical number of the ratio between the driving force for the Marangoni flow and the friction of film elements that move relative to their surroundings. This ratio is called the Mysels number. A linear stability analysis leads to a scaling relation lambda approximately h(Ca)(-1/3) between the wavelength lambda of the instability and the capillary number Ca (Ca=/etaV(s)/gamma. In experiments with several Marangoni-driven instabilities this scaling relation has been found; it illustrates the general applicability in the understanding of flow phenomena of this type. Copyright 2001 Academic Press.

Journal Article↗

PubMedDate not supplied

Effect of oxidation rate on cross-linking of mussel adhesive proteins.

The cross-linking behavior of mussel adhesive protein Mefp-1 was studied by measuring the rate of aggregation of the protein by photon correlation spectroscopy. To be able to calculate the aggregation numbers, the hydrodynamic radius of monomer Mefp-1 (10 nm) was determined under reducing conditions. The aggregation is controlled by the redox potential of the solution, and the aggregation number varied, independent of pH, over a factor 2 within the experimentally accessible redox potential window. A kinetic model for cross-linking, based on the intricate interplay of the oxidation and auto-oxidation of the hydroquinones of Mefp-1, is proposed. The oxidation rate strongly depends on redox potential. The cross-linking rate is taken to be proportional to the rate of auto-oxidation. The model correctly predicts the experimentally observed phenomena. When the oxidation rate is slower than the auto-oxidation rate, cross-linking is efficient and controlled by the oxidation rate. When the rate of auto-oxidation rate is slower than the oxidation rate, the cross-linking is inefficient due to the quick exhaustion of the hydroquinones. The experimentally determined rate constant for cross-linking is found to be much smaller than those found for auto-oxidation of hydroquinones because of the excluded volume interactions imposed by the protein backbone. Tuning the interplay between oxidation and auto-oxidation presents the potential of controlling cross-linking density independent of the density of reactive groups.

Animals↗