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Yayın A thermo-mechanical model of drill margin-borehole surface interface contact conditions in dry drilling of thick CFRP laminates(Elsevier Ltd, 2020-04-23) Karpat, Yiǧit; Karagüzel, Umut; Bahtiyar, OnurDry drilling of thick carbon fiber reinforced polymer (CFRP) laminates requires careful selection of process parameters in order to obtain acceptable borehole surface quality. Complex contact conditions between the drill margin and the borehole surface determine the integrity of the borehole surface depending on the process parameters and temperature-dependent viscoelastic material properties. Temperature rise during dry drilling reduces the elastic modulus of the CFRP and causes thermal expansion of the drill, resulting in considerable contact length at the drill margin and borehole surface interface. Manufacturers need a better understanding of the interaction among contact pressure, sliding velocity, temperature at the interface, and temperature-dependent material properties to develop predictive models for drilling CFRPs. To examine this complex interaction, this study develops a novel, hybrid model that combines a time-based analytical modeling of drilling process with a finite element-based modeling of temperature rise. Drilling experiments were performed in which thrust force, torque, and temperature were measured as a function of feed, and these measurements were used to identify unknown hybrid model parameters. The results revealed that a significant change in friction conditions occurs when increased temperatures at the margin and borehole surface interface approach and exceed the glass transition temperature of the CFRP laminate at a large feed rate. These findings show the benefit of increasing feed during dry drilling, which is nonetheless limited by the temperature-dependent material properties of the work material.Yayın Theoretical calculation of the kinetic coefficient of normal crystal growth(Trans Tech Publications Ltd, 2004) Dimitrov, Ventzislav IvanovAn expression for the velocity u of migration of a diffuse simple crystal-melt interface has been derived on the basis of the theory of atomic mobility in supercooled liquids: u = K-0 (T / T-m) DeltaT, where DeltaT = T-m - T the undercooling below the melting point T-m; K-0 is the kinetic coefficient of atomic attachment, which is used in models of crystal growth. It has been calculated for a number of metals. u(max) = K0Tm / 4 is the theoretical limit of the velocity of crystal growth. For a number of FCC metals the theoretical limit of crystal growth has been found to be of order of 200 m/s. The crystal growth kinetics has been shown to be limited by the atomic self-diffusion in the interface, for which the strong dependence on the orientation of the crystal/melt interface has been explained.Yayın A photon transmission study for film formation from poly(vinyl acetate) latex particles with different molecular weights(John Wiley & Sons Inc, 2007-10-15) Arda, Ertan; Kara, Selim; Pekcan, Mehmet ÖnderThe photon transmission technique was used to monitor the temperature evolution of film formation from poly(vinyl acetate) (PVAc) latex particles with two different molecular weights. Two sets of latex films were prepared below the glass transition temperature (T-g) of PVAc, which are named as low (LM) and high molecular weight (HM) films. These films were annealed at elevated temperatures above the Tg of PVAc for various time intervals. It is observed that transmitted photon intensity (I-tr) from these films increased as the annealing temperature was increased. Onset temperatures (T-H) at given times (tau H) for starting the optical clarity of LM and HM films were measured and used to calculate the healing activation energies (Delta H) for the PVAc minor chains, and found to be as 28.1 kcal/mol and 27.7 kcal/mol, respectively. The increase in the transmitted photon intensity, Itr above TH was attributed to the increase in the number of disappeared interfaces between the deformed latex particles. Prager-Tirrell (PT) model was employed to interpret the increase in the crossing density of chains at the junction surfaces. The interdiffusion (backbone) activation energies (Delta E) were measured and found to be 177.5 kcal/mol and 210.7 kcal/mol for a diffusing PVAc chains across the junction surface of LM and HM latex films, respectively.Yayın Film formation from TiO2-polystyrene latex composite: a fluorescence study(Taylor & Francis Group, 2007-03-01) Uğur, Şaziye; Sunay Yapışkan, Münüre Selin; Tepehan, Fatma Zehra; Pekcan, Mehmet ÖnderThis work reports the use of the steady state fluorescence (SSF) technique for studying film formation from TiO2 covered polystyrene (PS) latex particles. The composite films were prepared from pyrene (P)-labeled PS particles by covering them with TiO2 at room temperature and then annealed at elevated temperatures in 10 min time interval above glass transition (T-g) temperature of polystyrene. Five different composite films were studied in various TiO2 layer contents. Fluorescence intensities Ip from P were measured after each annealing step to monitor the stages of film formation. Films showed considerable increase in Ip above the certain onset temperature called minimum film forming temperature, T-0. Void closure and interdiffusion stages were modeled and related activation energies were determined and found to be 23.12 and 92.80 kJ mol(-1), respectively.Yayın Theory of fluidity of liquids, glass transition, and melting(Elsevier B.V., 2006-03-01) Dimitrov, Ventzislav IvanovThis is a presentation of a rigorous theory of fluidity of liquids, glass transition and melting of solids in the frame of an asymmetric double well potential model. Potential wells are doubled time to time by the local density fluctuations caused by the thermal longitudinal waves. The average frequency of doubling of potential wells is equal to the frequency of the most energetic waves which obey a law similar to Wein's displacement law in black body radiation. Based on the equilibrium thermodynamic theory of fluctuations and the displacement law, a law of linear pre-diffusion mean-square displacement of particles in a solid is derived: the mean-square displacement of molecules within their potential wells increases linearly with temperature. It is shown that when this is broken-down (where the mean-square displacement at a certain temperature rapidly changes its slope as a function of temperature) glass devitrifies and crystal melts, and all possible solid-liquid transitions of a substance occur at the same critical mean-square displacement: any solid (not only crystals) transforms into liquid when the mean-square displacement, as a fraction of the average intermolecular distance, acquires a certain universal critical value - the same for different substances. It is proved that molecules in a liquid perform specific Brownian motion. The average jump distance is a function of temperature and it is much smaller than the nearest intermolecular distances. At a certain temperature, shown to be the Kauzmann temperature, the average jump distance of Brownian motion becomes equal to zero: the supercooled liquid undergoes glass transition. The transition was proven to be a phase transition of the fourth order: the free energy of the system and its first, second and third derivatives are all continuous functions, but its fourth derivative with respect to temperature is discontinuous. Molecular mobility, diffusion and viscosity are obtained as functions of temperature.Yayın Molecular alignment during gel formation from methyl methacrylate: An excimer fluorescence study(Taylor & Francis Ltd, 2005-05) Kaya Aktaş, Demet; Erdoğan, Matem; Pekcan, Mehmet ÖnderGlass transition during bulk polymerization was studied in free-radical cross-linking copolymerization (FCC) of methyl methacrylate (MMA) using the steady-state fluorescence (SSF) technique. Naphthalene (N) was used as a monomer and excimer forming probe. Changes in the viscosity of the pregel solutions due to gel formation dramatically enhance both monomer and excimer fluorescent yield of N molecules. The reaction time at which the monomer and excimer intensities exhibit a sudden increase corresponds to the reaction time at which the rate of polymerization becomes maximum resulting from the gel effect. This effect was used to study the gelation of MMA, as a function of time, in various N concentrations. The results were interpreted in the view of percolation theory. The gel fraction, beta, and weight average degree of polymerization, gamma, exponents beta=0.40 +/- 0.02 and gamma=1.70 +/- 0.07 were found in agreement with percolation results for both monomer and excimer measurements, respectively.Yayın Percolation approach to film formation from surfactant-free polystyrene particles(Taylor & Francis, 2005-09) Uğur, Şaziye; Pekcan, Mehmet ÖnderIn this study, a film formation process from surfactant-free polystyrene (PS) latex particles is reported. Steady state fluorescence (SSF) and photon transmission (UVV) techniques were used to study the evolution of film formation. The latex films were prepared from pyrene (P)-labeled PS particles at room temperature and annealed at time intervals of 2.5 min above the glass transition temperature (T-g) of PS. During the annealing processes, the transparency of the film changed considerably. Fluorescence intensity (I-0P) from P was measured after each annealing step to monitor the stages of film formation. Evolution of transparency of latex films were monitored by using photon transmission intensity, I-tr. A drastic increase in I-tr and I-0P above the critical annealing times, t(r) and t(c) were attributed, respectively to percolation behavior of PS material from one side to the other side of the latex film. Critical exponents, beta of percolation clusters were measured and found to be around 0.35 and 0.25 for I-tr and I-0P measurements, respectively.Yayın Universal behaviour of glass transition exponents in various polymeric systems(VSP BV, Brill Academic Publishers, 2005) Pekcan, Mehmet Önder; Kaya Aktaş, DemetThe fast transient fluorescence (FTRF) technique was used to study the critical exponents during glass transition in free-radical cross-linking copolymerization (FCC). Methyl methacrylate (MMA), ethyl methacrylate (EMA) and various combinations of MMA with EMA were used during FCC experiments. Pyrene (Py) was used as a fluorescence probe and its fluorescence lifetimes from its decay traces were measured during glass transition. Changes in the viscosity of the pre-gel solutions due to glass formation dramatically increased the Py fluorescent lifetimes, which were used to study the glass transition of MMA, EMA and their mixtures as a function of time, at various temperatures and monomer concentrations. The results were interpreted in the view of percolation theory. The critical exponents, beta and gamma, were measured near the glass transition point and found to be around 0.37 +/- 0.015 and 1.69 +/- 0.05, respectively, in all systems studied, which are in good agreement with the static percolation results.Yayın Effects of annealing on morphology of polymer/polymer (PS/PMMA) blend; a fluorescence study(John Wiley& Sons Inc, 2006-05-05) Uğur, Şaziye; Pekcan, Mehmet ÖnderSteady state fluorescence (SSF) technique conjunction with optical microscopy were used to study the morphology of polystyrene (PS)/poly(methyl methacrylate) (PMMA) blend upon annealing above glass transition in elevated time intervals. The PS/PMMA blends were prepared from dissolution of pyrene (P) and naphthalene (N) labeled PS and PMMA particles, respectively. Monte Carlo Simulations were performed to model the N and P fluorescence intensities (I-N and I-P), Using photon diffusion theory. Number of N and P photons (N-N and N-P) emerging from the front surface of the blend are calculated when only N is excited, where N-P photons are combined of photons from radiative (N-PR) and nonradiative (N-PNR) energy transfer processes. Optical microscopy images were taken at each annealing step to Support Our findings from fluorescence measurements.Yayın Poly (styrene) latex/modified na-activated bentonite nanocomposite films: a fluorescence study(Elsevier Science BV, 2008-12) Uğur, Şaziye; Yargı, Önder; Günister, Ebru; Pekcan, Mehmet ÖnderWe studied film formation of composites of surfactant-free polystyrene (PS) nanoparticles and modified Na-activated bentonite (MLB), by steady state fluorescence (SSF) technique. The films were prepared from a mixture of pyrene (P)-labeled PS particles and MLB at various compositions at room temperature. These films were annealed at elevated temperatures above the glass transition (T(g)) temperature of polystyrene for 10 min. Scattered light (I(S)) and fluorescence intensities (I(P)) from P were measured after each annealing step to monitor the stages of film formation. Evolution of transparency of the composite films was monitored by using photon transmission intensity, I(tr) Atomic force microscopy (AFM) was used to detect the variation in physical structure of annealed composite films. The nanocomposite films exhibited a percolation threshold at 20 wt.% MLB content. Below this fraction two distinct film formation stages were observed which are known as void closure and interdiffusion and above this fraction no film formation was detected. At 0-20 wt.% MLB, minimum film formation, T(0), void closure, T(v) and healing, T(h) temperatures were determined. Void closure and interdiffusion stages were modeled and related activation energies were determined. Void closure activation energies decreased as the percent of MLB increased, no variation was observed in backbone activation energies.
