Abstract:The cooling rate dependence of the crystallinity of polymers is investigated via the example of different technical polypropylenes using fast scanning calorimetry (FSC) in a cooling rate range between 1 and 5000 K s 21 . In the slower cooling rate range (below 100 K s 21 ) the crystallinity increases slightly with decreasing cooling rate. Above cooling at 100 K s 21 the crystallinity decreases substantially and vanishes at the critical cooling rate. We describe this behavior using a simplified model with two c… Show more
“…As mentioned before, it is suggested that secondary crystallization proceeds only at slow cooling rates. Note, in the previous study, the cooling rate dependence of the crystallinity was described using a simple phenomenological model with generic crystallization function and retardation function . The form of the functions is different from the present equation.…”
Fast scanning calorimetry (FSC) has been used to investigate the kinetics of nonisothermal crystallization, isothermal crystallization, and melting for semicrystalline polymers (ie, poly(butylene terephthalate, polyphenylene sulfide, and isotactic polypropylene). The scanning rate dependence of enthalpy of melt‐crystallization, cold‐crystallization, and recrystallization obtained from FSC are quantitatively explained on the basis of Ozawa's method. For isothermal kinetics, FSC allows to obtain the annealing‐temperature dependence of crystallization half‐time in a wide range of the supercooling without any unwanted nucleation or crystallization during cooling. The effect of additives for nonisothermal or isothermal crystallization was also considered in this article. In addition, hyphenated technique of FSC and polarized optical microscopy clearly shows the differences in crystallization kinetics and morphologies.
“…As mentioned before, it is suggested that secondary crystallization proceeds only at slow cooling rates. Note, in the previous study, the cooling rate dependence of the crystallinity was described using a simple phenomenological model with generic crystallization function and retardation function . The form of the functions is different from the present equation.…”
Fast scanning calorimetry (FSC) has been used to investigate the kinetics of nonisothermal crystallization, isothermal crystallization, and melting for semicrystalline polymers (ie, poly(butylene terephthalate, polyphenylene sulfide, and isotactic polypropylene). The scanning rate dependence of enthalpy of melt‐crystallization, cold‐crystallization, and recrystallization obtained from FSC are quantitatively explained on the basis of Ozawa's method. For isothermal kinetics, FSC allows to obtain the annealing‐temperature dependence of crystallization half‐time in a wide range of the supercooling without any unwanted nucleation or crystallization during cooling. The effect of additives for nonisothermal or isothermal crystallization was also considered in this article. In addition, hyphenated technique of FSC and polarized optical microscopy clearly shows the differences in crystallization kinetics and morphologies.
“…Under the high supercooling (low curing temperature), there was not enough time to adjust the crystal structure between the PA 6 molecular chains; consequently, the amorphous structure was formed. In contrast, under low supercooling, a more stable crystal structure was formed . Therefore, the degree of crystallinity of PA 6 increased in proportion to the curing temperature.…”
The thermoplastic resin transfer molding (T‐RTM) process for carbon fiber reinforced thermoplastic polymer composites (CFRTP) were experimentally investigated and optimized using high‐pressure resin transfer molding system for mass production. The CFRTP was manufactured by Anionic ring opening polymerization of the T‐RTM process and the curing process was analyzed by in situ cure monitoring using dielectrometry. Mechanical properties, productivity, and crystal structures of the PA 6 matrix and CFRTP were evaluated by differential scanning calorimetry, X‐ray diffraction analysis, tensile, and interlaminar shear strength tests. The crystallinity, impregnation quality and process speed were determined by the curing temperature. In addition, a time‐ and cost‐effective flame surface treatment was developed to remove moisture from the carbon fiber and increase the interfacial bonding strength of the CFRTP. As a result, optimal T‐RTM processing conditions were suggested for realizing maximum productivity and mechanical properties for the CFRTP.
“…The crystallinity was calculated by measuring the melting enthalpy and comparing that with the melting enthalpy of 100% crystalline PCL, as reported in the literature . In general, the degree of crystallinity as the polymer melt cools down below the melting point during electrospinning due to convective heat loss may depend on the cooling rate experienced by the polymer . Faster cooling rates reduce the time that crystals are allowed to form, and it may lead to reduced crystallinity.…”
Section: Resultsmentioning
confidence: 99%
“…[52] In general, the degree of crystallinity as the polymer melt cools down below the melting point during electrospinning due to convective heat loss may depend on the cooling rate experienced by the polymer. [53] Faster cooling rates reduce the time that crystals www.advancedsciencenews.com www.mme-journal.de are allowed to form, and it may lead to reduced crystallinity. Thus, thinner fibers might be at a disadvantage due to their higher surface to volume ratio which increases the rate of heat loss.…”
Section: Effect Of Spinneret Architecture On Crystallinitymentioning
Here, a novel melt electrospinning method to produce few‐micron and nanometer thick fibers is presented, in which a polymer‐coated wire with a sharp tip is used as the polymer source. The polymer coating is melted via Joule heating of the source wire and extracted toward the target via electrostatic forces. The high viscosity and low charge density of polymer melts lower their stretchability in melt. The method relies on confining the Taylor cone and reducing initial jet diameter via concentrated electrostatic fields as a means to reduce the diameter of fibers. As a result, the initial jet diameter and the final fiber diameter are reduced by an order of magnitude of three to ten times, respectively, using wire melt electrospinning compared to syringe‐ and edge‐based electrospinning. The fiber diameter melt electrospun via this novel method is 1.0 ± 0.9 µm, considerably thinner than conventional melt electrospinning techniques. The generation of thin fibers are explained in terms of the electrostatic field around the wire tip, as obtained from finite element analysis (FEA), which controls the size and shape of the melt electrospun jet.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.