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Biomedical subjects

O Pekcan

Publications and source records attributed to O Pekcan.

7 recordsLinked to original sources
PubMed2005

Ceramic encapsulated latex composites.

This work reports the encapsulation of latex particles in Al2O3-polystyrene (PS) composite films. These films were prepared from PS particles in Al2O3 dispersion at room temperature in various latex contents. Composite films were annealed at elevated temperatures in 10 min time interval above the glass transition temperature (Tg) of polystyrene. Transmitted photon intensities, I(tr) were monitored after each annealing step. AFM micrographs were also used to observe the physical changes of the composite films during annealing. It was observed that latex particles are encapsulated above a critical Al2O3 content of 33 wt% which corresponds to the critical occupation probability of p(c) = 0.33 at which the film obey the site-percolation model with a critical exponent of 0.45. Below p(c), it was seen that complete latex film formation process took place, where transparency of the film was increased by annealing.

Journal Article↗
PubMed2004

A fluorescence study on the gel-to-sol transition of kappa-carrageenan.

The fluorescence technique was employed to study gel-to-sol transitions in kappa-carrageenan systems with various carrageenan contents. Pyranine was used as a fluorescence probe for monitoring these transitions. Fluorescence, Ip and scattered light, Isc intensities were measured against temperature to determine critical phase transition temperatures and exponents. It was observed that gel-to-sol transition temperatures, Tgs are found to be dependent to the carrageenan content. The measured critical exponents gamma' and beta' were found to be very close to the weight average degree of polymerization, DPw and gel fraction G, exponents (gamma and beta) of the classical Percolation Model.

Carrageenan↗
PubMed2002

Fast transient fluorescence technique (FTRF) for studying vapor-induced latex film formation.

A fast transient fluorescence (FTRF) technique was used to study latex film formation induced by organic solvent vapor. Seven different films with the same latex content were prepared separately from poly(methyl methacrylate) (PMMA) particles and exposed to vapor of various chloroform-heptane mixtures in seven different experiments. Latex films were prepared from pyrene (Py)-labeled latex particles and fluorescence lifetimes of Py were monitored during vapor-induced film formation. It was observed that pyrene lifetimes decreased as vapor exposure time increased. A Stern-Volmer kinetic analysis was used for low quenching efficiencies to interpret the decrease in pyrene lifetimes. A Prager-Tirrel model was employed to obtain back-and-forth frequencies, nu, of the reptating PMMA chains during latex film formation induced by solvent vapor. nu values were found to be correlated with chloroform content in vapor mixture. It was observed that polymer interdiffusion obeyed a t(1/2) law during film formation. The results of optical transmission experiments were found to support these findings.

Journal Article↗
PubMed2002

Molecular weight effect on latex film formation induced by solvent vapor: an optical transmission study.

Two different sets of powder latex film were prepared from high- and low-molecular-weight (HM and LM) poly(methyl methacrylate) (PMMA). The optical transmission method was used to the study film formation induced by organic vapor. Various HM and LM films with the same latex content were prepared separately from the PMMA particles and exposed to vapor of a chloroform-heptane mixture in various volume percents of chloroform. Transmitted light intensities, I(tr), from these films increased in time under vapor exposure, which was attributed to the increase in "crossing density" at the junction surface. The Prager-Tirrell model was employed to obtain the back-and-forth frequency, nu, of the reptating polymer chain during film formation induced by solvent vapor. nu values were obtained and found to be strongly correlated with the percent of chloroform in the solvent mixture and the molecular weight of the polymer chain. It is observed that high-molecular-weight chains reptate much more slowerly than low-molecular-weight chains.

Journal Article↗
PubMed2002

Slow regions percolate near glass transition.

A nanosecond scale in situ probe reveals that a bulk linear polymer undergoes a sharp phase transition as a function of the degree of conversion, as it nears the glass transition. The scaling behaviour is in the same universality class as percolation. The exponents gamma and beta are found to be 1.7 +/- 0.1 and 0.41 +/- 0.01 in agreement with the best percolation results in three dimensions.

Journal Article↗
PubMed1999

Photon transmission technique for studying multiple phase transitions in a liquid crystal.

A photon transmission technique was used to monitor the multiple phase transitions in a 4-butoxyphenyl4(')-declyoxybenzoate (BOPDOB) liquid crystal. Drastic decreases in the transmitted photon intensity (I) were attributed to the sequential phase transitions in BOPDOB upon cooling. In this paper, it is assumed that the order parameter rho is proportional to the transmitted photon intensity. The isotropic-nematic and nematic-smectic-A transitions were observed and found to be of first order. It was observed that the smectic-A-smectic-C and smectic-C-smectic-G transitions are second order. It was found that for the smectic-A-smectic-C transition, critical exponent crosses over from beta=0.513+/-0.006, which is consistent with mean-field theory, to beta=0.35+/-0.009, which is consistent with heliumlike behavior, as the Ginzburg criterion predicts. The critical exponent for the smectic-C-smectic-G transition was found to be beta=0.703+/-0.001. Transition temperatures were established at each phase transitions and found to be 84.92 degrees C, 74.85 degrees C, 52.96 degrees C, and 33.03 degrees C for isotropic-nematic, nematic-smectic-A, smectic-A-smectic-C and, smectic-C-smectic-G transitions, respectively.

Journal Article↗