01971nas a2200193 4500008004100000022001400041245005200055210005200107260008600159300001200245490000800257520134300265653000901608653002801617653001501645653001001660100002701670856008001697 2005 eng d a1532-179700aCrystallization of polymers from stressed melts0 aCrystallization of polymers from stressed melts a325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USAbTAYLOR & FRANCIS INCcOCT a375-3970 vC453 a

In the last decade, there have been several investigations into the route by which a polymer melt that has been subjected to flow transforms into a crystalline state. Crystallization of polymers from flowing or stressed melts is a technologically important problem since most thermoplastics are subjected to intense flow fields during normal processing operations. The renewed interest in this problem is due to the availability of new experimental tools that, coupled with advances in modeling and simulations, are beginning to yield insights into the molecular characteristics that control the crystallization pathways adopted by a stressed polymer melt. Recent evidence conclusively implicates the high molecular weight tail in promoting crystallization on shearing. It appears that the formation of oriented nuclei in polydisperse melts is controlled by chain orientation of a small fraction of high molecular weight chains in a melt. Thus, it is the theological criteria for ``critical'' chain orientation that govern flow-induced acceleration and orientation in polymer crystallization. This review summarizes the literature on the effect of shearing on polymer crystallization, and focuses on recent advances in understanding the role of molecular parameters that couple polymer crystallization to flow and melt orientation.

10aflow10apolymer crystallization10aprocessing10ashear1 aKumaraswamy, Guruswamy uhttp://library.ncl.res.in/content/crystallization-polymers-stressed-melts-102766nas a2200265 4500008004100000022001400041245005700055210005700112260000800169490000700177520201300184653001302197653002002210653002202230653001902252653001302271653000902284653002002293653001702313653000902330100002802339700001802367700002702385856008802412 2017 eng d a1744-683X00aCapillary uptake in macroporous compressible sponges0 aCapillary uptake in macroporous compressible sponges cSEP0 v133 a

The capillarity-driven uptake of liquid in swellable, highly porous sponges is of significant industrial importance. Sponges prepared using polymers and their composites with carbon nanotubes and graphene have been reported, with extraordinary solvent uptake capacities and with the ability to separate oil from water. However, the effect of systematic variation of sponge characteristics on solvent uptake has not been investigated. Here, we report experiments that study capillary uptake in a variety of flexible, centimetre-sized macroporous cylindrical sponges. We used ice-templating to prepare a series of model macroporous sponges in which the porosity, modulus and composition were systematically varied. We investigated two kinds of sponge: (a) those composed purely of cross-linked polymers and (b) those prepared as composites of inorganic particles and polymers. Both kinds of sponge are flexible and exhibit elastic recovery after large compressive deformation. All sponges were characterized thoroughly with respect to their pore microstructure and elastic modulus. When one end of a sponge is plunged into a large reservoir, water rises through capillary action against gravity. We observed a transition from an inertial capillary regime, where the liquid column height rose linearly with time, t, to a viscous capillary regime, where the liquid height rose with time t(0.5). We showed that these results can be rationalized using analyses developed for rigid sponges. We combined differential momentum balance equations for uptake in rigid capillaries with the phenomenological Ergun-Forchheimer relations to account for the effect of the sponge microstructure. This approach works remarkably well in the viscous capillary regime and shows that capillary uptake is governed primarily by the total porosity and pore dimensions of soft sponges.

10aaerogels10aBuilding blocks10aCatalyst Supports10aContact-angels10aDynamics10aflow10aOrganic Liquids10aPorous-Media10aRise1 aChatterjee, Soumyajyoti1 aDoshi, Pankaj1 aKumaraswamy, Guruswamy uhttp://library.ncl.res.in/content/capillary-uptake-macroporous-compressible-sponges