02175nas a2200193   4500008004100000245009800041210006900139260011800208300002700326490000900353520137500362100002701737700001801764700002201782700001801804700001801822700001701840856012401857       2015                        eng d00aInfluence of macromolecular architecture on necking in polymer extrusion film casting process0 aInfluence of macromolecular architecture on necking in polymer e  aCleveland, OHbAmerican Institute of Physics, 2 Huntington Quadrangle, STE 1No1, Melville, NY 11747-4501 USAcJUN  aArticle Number: 0800060 v16643 a<p>Extrusion film casting (EFC) is an important polymer processing technique that is used to produce several thousand tons of polymer films/coatings on an industrial scale. In this research, we are interested in understanding quantitatively how macromolecular chain architecture (for example long chain branching (LCB) or molecular weight distribution (MWD or PDI)) influences the necking and thickness distribution of extrusion cast films. We have used different polymer resins of linear and branched molecular architecture to produce extrusion cast films under controlled experimental conditions. The necking profiles of the films were imaged and the velocity profiles during EFC were monitored using particle tracking velocimetry (PTV) technique. Additionally, the temperature profiles were captured using an IR thermography and thickness profiles were calculated. The experimental results are compared with predictions of one-dimensional flow model of Silagy et al(1) wherein the polymer resin rheology is modeled using molecular constitutive equations such as the Rolie-Poly (RP) and extended Pom Pom (XPP). We demonstrate that the 1-D flow model containing the molecular constitutive equations provides new insights into the role of macromolecular chain architecture on film necking. D-1. Silagy, Y. Demay, and J-F. Agassant, Polym. Eng. Sci., 36, 2614 (1996).</p>1 aPol, Harshawardhan, V.1 aBanik, Sourya1 aAzad, Lal, Busher1 aThete, Sumeet1 aDoshi, Pankaj1 aLele, Ashish  uhttps://library.ncl.res.in/content/influence-macromolecular-architecture-necking-polymer-extrusion-film-casting-process03148nas a2200217   4500008004100000022001400041245013200055210006900187260006700256300001400323490000800337520227200345653002402617653003202641653005102673100001902724700001802743700002002761700002102781856012802802       2015                        eng d  a0006-359200aInterlinked population balance and cybernetic models for the simultaneous saccharification and fermentation of natural polymers0 aInterlinked population balance and cybernetic models for the sim  a111 RIVER ST, HOBOKEN 07030-5774, NJ USAbWILEY-BLACKWELLcOCT  a2084-21050 v1123 a<p>Simultaneous Saccharification and Fermentation (SSF) is a process where microbes have to first excrete extracellular enzymes to break polymeric substrates such as starch or cellulose into edible nutrients, followed by in situ conversion of those nutrients into more valuable metabolites via fermentation. As such, SSF is very attractive as a one-pot synthesis method of biological products. However, due to the co-existence of multiple biochemical steps, modeling SSF faces two major challenges. The first is to capture the successive chain-end and/or random scission of the polymeric substrates over time, which determines the rate of generation of various fermentable substrates. The second is to incorporate the response of microbes, including their preferential substrate utilization, to such a complex broth. Each of the above-mentioned challenges has manifested itself in many related areas, and has been competently but separately attacked with two diametrically different tools, i.e., the Population Balance Modeling (PBM) and the Cybernetic Modeling (CM), respectively. To date, they have yet to be applied in unison on SSF resulting in a general inadequacy or haphazard approaches to examine the dynamics and interactions of depolymerization and fermentation. To overcome this unsatisfactory state of affairs, here, the general linkage between PBM and CM is established to model SSF. A notable feature is the flexible linkage, which allows the individual PBM and CM models to be independently modified to the desired levels of detail. A more general treatment of the secretion of extracellular enzyme is also proposed in the CM model. Through a case study on the growth of a recombinant Saccharomyces cerevisiae capable of excreting a chain-end scission enzyme (glucoamylase) on starch, the interlinked model calibrated using data from the literature (Nakamura et al., Biotechnol. Bioeng. 53:21-25, 1997), captured features not attainable by existing approaches. In particular, the effect of various enzymatic actions on the temporal evolution of the polymer distribution and how the microbes respond to the diverse polymeric environment can be studied through this framework. Biotechnol. Bioeng. 2015;112: 2084-2105. (c) 2015 Wiley Periodicals, Inc.</p>10acybernetic modeling10apopulation balance modeling10asimultaneous saccharification and fermentation1 aHo, Yong, Kuen1 aDoshi, Pankaj1 aYeoh, Hak, Koon1 aNgoh, Gek, Cheng  uhttps://library.ncl.res.in/content/interlinked-population-balance-and-cybernetic-models-simultaneous-saccharification-and-0