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Relevant bibliographies by topics / Polymer in dilute solution

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Academic literature on the topic 'Polymer in dilute solution'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Polymer in dilute solution"

1

Cotts, P. M., and J. C. Selser. "Polymer-polymer interactions in dilute solution." Macromolecules 23, no. 7 (April 1990): 2050–57. http://dx.doi.org/10.1021/ma00209a029.

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Halun, Joanna, Pawel Karbowniczek, Piotr Kuterba, and Zoriana Danel. "Investigation of Ring and Star Polymers in Confined Geometries: Theory and Simulations." Entropy 23, no. 2 (February 19, 2021): 242. http://dx.doi.org/10.3390/e23020242.

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The calculations of the dimensionless layer monomer density profiles for a dilute solution of phantom ideal ring polymer chains and star polymers with f=4 arms in a Θ-solvent confined in a slit geometry of two parallel walls with repulsive surfaces and for the mixed case of one repulsive and the other inert surface were performed. Furthermore, taking into account the Derjaguin approximation, the dimensionless layer monomer density profiles for phantom ideal ring polymer chains and star polymers immersed in a solution of big colloidal particles with different adsorbing or repelling properties with respect to polymers were calculated. The density-force relation for the above-mentioned cases was analyzed, and the universal amplitude ratio B was obtained. Taking into account the small sphere expansion allowed obtaining the monomer density profiles for a dilute solution of phantom ideal ring polymers immersed in a solution of small spherical particles, or nano-particles of finite size, which are much smaller than the polymer size and the other characteristic mesoscopic length of the system. We performed molecular dynamics simulations of a dilute solution of linear, ring, and star-shaped polymers with N=300, 300 (360), and 1201 (4 × 300 + 1-star polymer with four arms) beads accordingly. The obtained analytical and numerical results for phantom ring and star polymers are compared with the results for linear polymer chains in confined geometries.

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Armistead, J. P., R. R. Price, O. K. Kim, and L. S. Choi. "Shear-induced changes in chain configuration of poly(acrylic acid) in dilute solution." Proceedings, annual meeting, Electron Microscopy Society of America 47 (August 6, 1989): 698–99. http://dx.doi.org/10.1017/s0424820100155463.

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Small amounts (less than 30 ppm) of polymer dissolved in solution may significantly reduce the work required to pump fluids through a pipe at a given rate. In other words, the drag of the solution along the pipe walls is reduced. Drag reduction by polymers has been well characterized, however the molecular origin of the phenomena is not fully understood. Polymers that exhibit drag reduction characteristics typically have high molecular weight, have predominantly linear, flexible chains, and have an expanded molecular configuration in solution.Work in this laboratory has focused on the drag reduction behavior of poly(acrylic acid), PAA, in recent years. This polymer is one of the most shear stable water-soluble polymers and due to the ionic groups in the polymer chain its conformation in solution changes with pH and ionic strength. In a recent work, PAA solutions of 18 ppm, pH=8.1, showed an initial drag reduction of over thirty-five percent in rotating disc experiments. Over four minutes of shearing the drag reduction decreased to ten percent. This was surprising because of the known shear stability of PAA. When the sheared solution was left undisturbed for two weeks, it did not recover its drag reduction performance. However, the addition of NaCl to the solution during the shearing immediately restored drag reduction to its initial level. It was hypothesized that the shear flow induced interchain association that was possibly stabilized by hydrogen bonding and that the addition of the NaCl caused dissociation and drag reduction recovery. In additional work, fluorescence probe studies showed that shear flow induced local chain rigidity in the originally flexible polymer chains. In this study, the drag reduction experiments were repeated and the configurations of the sheared and unsheared polymer chains were viewed using electron microscopy.

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Bolisetty, Sreenath, Sabine Rosenfeldt, Christophe N. Rochette, Ludger Harnau, Peter Lindner, Youyong Xu, Axel H. E. Müller, and Matthias Ballauff. "Interaction of cylindrical polymer brushes in dilute and semi-dilute solution." Colloid and Polymer Science 287, no. 2 (December 6, 2008): 129–38. http://dx.doi.org/10.1007/s00396-008-1962-3.

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OUELLETTE, NICHOLAS T., HAITAO XU, and EBERHARD BODENSCHATZ. "Bulk turbulence in dilute polymer solutions." Journal of Fluid Mechanics 629 (June 15, 2009): 375–85. http://dx.doi.org/10.1017/s0022112009006697.

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By tracking small particles in the bulk of an intensely turbulent laboratory flow, we study the effect of long-chain polymers on the Eulerian structure functions. We find that the structure functions are modified over a wide range of length scales even for very small polymer concentrations. Their behaviour can be captured by defining a length scale that depends on the solvent viscosity, the polymer relaxation time and the Weissenberg number. This result is not captured by current models. Additionally, the effects we observe depend strongly on the concentration. While the dissipation-range statistics change smoothly as a function of polymer concentration, we find that the inertial-range values of the structure functions are modified only when the concentration exceeds a threshold of approximately 5 parts per million (p.p.m.) by weight for the 18 × 106 atomic mass unit (a.m.u.) molecular weight polyacrylamide used in the experiment.

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Yun, Seok Il, Robert M. Briber, R. Andrew Kee, and Mario Gauthier. "Dilute-solution structure of charged arborescent graft polymer." Polymer 47, no. 8 (April 2006): 2750–59. http://dx.doi.org/10.1016/j.polymer.2006.02.018.

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HONDA, Itsuro, Hiroki MORI, and Yosuke KAWASHIMA. "1207 Numerical Analysis of Dilute Polymer Solution Flow." Proceedings of Conference of Kansai Branch 2004.79 (2004): _12–13_—_12–14_. http://dx.doi.org/10.1299/jsmekansai.2004.79._12-13_.

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Zimm, Bruno H., and Ralph W. Kilb. "Dynamics of branched polymer molecules in dilute solution." Journal of Polymer Science Part B: Polymer Physics 34, no. 8 (June 1996): 1367–90. http://dx.doi.org/10.1002/polb.1996.913.

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Grisafi, S. "A sphere buoyant in a dilute polymer solution." Journal of Applied Polymer Science 40, no. 56 (September 5, 1990): 781–88. http://dx.doi.org/10.1002/app.1990.070400514.

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Du, Miao, Yasuyuki Maki, Taiki Tominaga, Hidemitsu Furukawa, Jian Ping Gong, Yoshihito Osada, and Qiang Zheng. "Friction of Soft Gel in Dilute Polymer Solution." Macromolecules 40, no. 12 (June 2007): 4313–21. http://dx.doi.org/10.1021/ma0702187.

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Dissertations / Theses on the topic "Polymer in dilute solution"

1

YANG, ZHENGNAN. "Kinetics of Polymer Chain Collapse in Dilute Solution." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1509377014210034.

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Zhao, Jiuzhou. "Convective Assembly of Rod-shaped Melanosome in Dilute Polymer Solution." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1462211308.

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Huang, Jin. "Extensional viscosity of dilute polymer solutions." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0004/MQ46075.pdf.

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Harris, Owen John. "Unsteady flows of dilute polymer solutions." Thesis, University of Cambridge, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319993.

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Harlen, Oliver Guy. "Strong flows of dilute polymer solutions." Thesis, University of Cambridge, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358648.

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Yu, Kui 1967. "Multiple morphologies of polystyrene-b-poly(ethylene oxide) diblock copolymers in dilute solution." Thesis, McGill University, 1998. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=36076.

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Multiple morphologies of self-assembled aggregates of polystyrene- b-poly(ethylene oxide) (PS-b-PEO) diblock copolymers in dilute solution have been studied. The PS blocks are relatively long compared to the PEO blocks. The aggregates are prepared by the addition of water or methanol to the copolymer solutions in N,N-dimethylformamide (DMF), dioxane, or tetrahydrofuran (THF) to induce the aggregation of the PS blocks. Aqueous solutions of the aggregates are obtained by dialysis with water. Morphologies are directly studied by transmission electron microscopy (TEM).
The morphogenic effect of the copolymer composition indicates that as the EO content in the diblock decreases, the morphology of the self-assembled aggregates changes progressively through spheres, rods, bilayers, and ultimately to inverted aggregates. The observed bilayers include lamellae, vesicles, tubules and large compound vesicles (LCVs), and the inverted aggregates include inverted (hollow) hoops with a hexagonal array and large compound micelles (LCMs).
The morphological transition from vesicles to inverted hoops is investigated, and a three-step mechanism is proposed. This mechanism involves a thickening of the vesicle walls accompanied by the formation of the hollow rods in the walls, and a decrease in the size of the original water core. Possible mechanisms of the formation of large vesicles from lamellae, as well as tubules and LCVs from vesicles are discussed.
The formation of the self-assembled aggregates with various morphologies is believed to be mainly controlled by the balance of three interactions arising from the core, the corona, and the core-solvent interface. Any factors, such as the addition of salt, which affect the balance will cause morphological changes. Accordingly, the morphogenic effects of added electrolytes, temperature, the common solvent, and the precipitant are studied. The study shows that various morphologies can be prepared from one diblock copolymer.

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Whang, Kyu-ho. "Static and Flow Properties of Dilute Polymer Solutions." Thesis, University of North Texas, 1991. https://digital.library.unt.edu/ark:/67531/metadc501073/.

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Small weight percentages of certain high-molecular weight polymers added to liquids in turbulent flow through conduits can result in dramatic friction reduction. Although many current and potential uses of the drag reduction phenomenon exist, there is a fundamental problem: drag reduction efficacy decreases rapidly with flow time due to the mechanical degradation in flow of the added polymer. In this thesis study, dilute aqueous solutions of polyacrylamide were tested under turbulent flow conditions in an attempt to determine where mechanical degradation in flow occurs.

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Bhave, Aparna Vasant. "Kinetic theory for dilute and concentrated polymer solution study of nonhomogeneous effects." Thesis, Massachusetts Institute of Technology, 1992. http://hdl.handle.net/1721.1/12553.

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McKinley, Scott Alister. "An existence result from the theory of fluctuating hydrodynamics of polymers in dilute solution." Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1149020682.

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Ida, Daichi. "DILUTE SOLUTION PROPERTIES OF SEMIFLEXIBLE STAR POLYMERS." 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/66202.

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Kyoto University (京都大学)
0048
新制・課程博士
博士(工学)
甲第14170号
工博第3004号
新制||工||1446(附属図書館)
26476
UT51-2008-N487
京都大学大学院工学研究科高分子化学専攻
(主査)教授吉﨑武尚, 教授田中文彦, 教授伊藤紳三郎
学位規則第4条第1項該当

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Books on the topic "Polymer in dilute solution"

1

Huang, Jin. Extensional viscosity of dilute polymer solutions. Ottawa: National Library of Canada, 1999.

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Radwan, Mostafa Abdel-Salam. Characterisation of neutral and Zwitterionic polymers in dilute solution. Salford: University of Salford, 1991.

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Chanson, H. Drag reduction in self-aerated flows: Analogy with dilute polymer solutions and sediment laden flows. Brisbane: University of Queensland, Dept. of Civil Engineering, 1992.

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Chanson, H. Drag reduction in self-aerated flows: Analogy with dilute polymer solutions and sediment laden flows. Brisbane: Department of Civil Engineering, University of Queensland, 1992.

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Hao, Wen. Polymer solution data collection. Frankfurt/Main, Germany: DECHEMA, 1992.

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1959-, High Martin S., ed. Handbook of polymer solution thermodynamics. New York: Design Institute for Physical Property Data, American Institute of Chemical Engineers, 1993.

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Phillies, George D. J. Phenomenology of polymer solution dynamics. Cambridge: Cambridge University Press, 2011.

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Danner, Ronald P., and Martin S. High. Handbook of Polymer Solution Thermodynamics. Hoboken, NJ, USA: John Wiley & Sons, Inc., 1993. http://dx.doi.org/10.1002/9780470938232.

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Saaid, I. Mohd. Recovery of metal from dilute solution using porous electrode. Manchester: UMIST, 1998.

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Cloizeaux, Jacques Des. Polymers in solution: Their modelling and structure. Oxford: Clarendon Press, 1990.

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Book chapters on the topic "Polymer in dilute solution"

1

Gooch, Jan W. "Dilute-Solution Viscosity." In Encyclopedic Dictionary of Polymers, 225. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3695.

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Lodge, Timothy P., and Paul C. Hiemenz. "Dynamics of Dilute Polymer Solutions." In Polymer Chemistry, 377–438. Third edition. | Boca Raton : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9780429190810-9.

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3

Mandelkern, L., C. O. Edwards, R. C. Domszy, and M. W. Davidson. "Gelation Accompanying Crystallization from Dilute Solution: Some Guiding Principles." In Microdomains in Polymer Solutions, 121–41. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2123-1_8.

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Leal, L. Gary. "Dynamics of Dilute Polymer Solutions." In Structure of Turbulence and Drag Reduction, 155–85. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-50971-1_15.

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Buchhammer, Heide-M., Mandy Mende, and Marina Oelmann. "Preparation of monodisperse polyelectrolyte complex nanoparticles in dilute aqueous solution." In Aqueous Polymer Dispersions, 98–102. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b12146.

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Buchhammer, Heide-M., Mandy Mende, and Marina Oelmann. "Preparation of monodisperse polyelectrolyte complex nanoparticles in dilute aqueous solution." In Aqueous Polymer Dispersions, 98–102. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-540-36474-0_20.

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Zwanzig, Robert. "Langevin Theory of Polymer Dynamics in Dilute Solution." In Advances in Chemical Physics, 325–31. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470143605.ch17.

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Wachenfeld-Eisele, E., and W. Burchard. "Cured Epoxy Resins: Measurements in Dilute and Semidilute Solution." In Biological and Synthetic Polymer Networks, 305–19. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1343-1_20.

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Brouckère, L. De, and M. Mandel. "Dielectric Properties of Dilute Polymer Solutions." In Advances in Chemical Physics, 77–118. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470143476.ch3.

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Gampert, Bernhard, Thomas Eich, and Christoph Wilkes. "Elongational Behaviour of Dilute Polymer Solutions." In Science and Art Symposium 2000, 233–38. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4177-2_29.

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Conference papers on the topic "Polymer in dilute solution"

1

Hsu, Jui-Hung, Wunshain S. Fann, Kuen-Ru Chuang, and Shaw-An Chen. "Aggregated luminescence from light-emitting polymer in dilute solution." In Optical Science, Engineering and Instrumentation '97, edited by Z. Valy Vardeny and Lewis J. Rothberg. SPIE, 1997. http://dx.doi.org/10.1117/12.279293.

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Soulages, Johannes, Gareth McKinley, Nancy Hall, Kevin Magee, Gregory Chamitoff, and E. Fincke. "Extensional Properties of a Dilute Polymer Solution Following Preshear in Microgravity." In 48th AIAA Aerospace Sciences Meeting Including the New Horizons Forum and Aerospace Exposition. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2010. http://dx.doi.org/10.2514/6.2010-1107.

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Soulages, Johannes M., Gareth H. McKinley, Nancy R. Hall, Kevin S. Magee, Gregory E. Chamitoff, and E. Michael Fincke. "Extensional Properties of a Dilute Polymer Solution Following Preshear in Microgravity." In 12th Biennial International Conference on Engineering, Construction, and Operations in Challenging Environments; and Fourth NASA/ARO/ASCE Workshop on Granular Materials in Lunar and Martian Exploration. Reston, VA: American Society of Civil Engineers, 2010. http://dx.doi.org/10.1061/41096(366)202.

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Ryskin, G. "Pressure drop in the sink flow of a dilute polymer solution." In AIP Conference Proceedings Volume 137. AIP, 1986. http://dx.doi.org/10.1063/1.35518.

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Kabanemi, Kalonji K., Jean-Franc¸ois He´tu, and Samira H. Sammoun. "Experimental Study on Flow-Front Fingering Instabilities in Injection Molding of Polymer Solutions and Melts." In ASME 2004 International Mechanical Engineering Congress and Exposition. ASMEDC, 2004. http://dx.doi.org/10.1115/imece2004-59078.

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An experimental investigation of the flow behavior of dilute, semi-dilute and concentrated polymer solutions has been carried out to gain a better understanding of the underlying mechanisms leading to the occurrence of instabilities at the advancing flow front during the filling of a mold cavity. Experiments were performed using various mass concentrations of low and high molecular weight polyacrylamide polymers in corn syrup and water. This paper reports a new type of elastic fingering instabilities at the advancing flow front that has been observed only in semi-dilute polymer solutions of high molecular weight polymers. These flow front elastic instabilities seem to arise as a result of a mixture of widely separated high molecular weight polymer molecules and low molecular weight solvent molecules, which gives rise to a largely non-uniform polydisperse solution, with respect to all the kinds of molecules in the resulting mixture (solvent molecules and polymer molecules). The occurrence of these instabilities appears to be independent of the injection flow rate and the cavity thickness. Moreover, these instabilities do not manifest themselves in dilute or concentrated regimes, where respectively, polymer molecules and solvent molecules are minor perturbation of the resulting solution. In those regimes, smooth flow fronts are confirmed from our experiments. Based on these findings, the experimental investigations have been extended to polymer melts. Different mixtures of polycarbonate melts of widely separated molecular weights (low and high molecular weights) were first prepared. The effect of the large polydispersity of the resulting mixtures on the flow front behavior was subsequently studied. The same instabilities at the flow front were observed only in the experiments where a very small amount of high molecular weight polycarbonate polymer has been mixed to a low molecular weight polycarbonate melt (oligomers).

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Watanabe, Keizo, Satoshi Ogata, and Munehiko Hirao. "Flow Characteristics of Dilute Polymer Solutions in Micro Tubes." In ASME/JSME 2007 5th Joint Fluids Engineering Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/fedsm2007-37033.

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Pressure drops and velocity profiles for micro tubes were investigated for the laminar flow of distilled water and dilute polymer solutions. The test micro tubes were fused silica capillaries with diameters in the range of 50.2–251.8 μm, and a value of l/d (length/diameter) of about 340. By performing pressure drop measurements, it is shown that the experimental data agree well with the Hagen-Poiseuille equation in the case of Newtonian fluids. On the other hand, the flow rate of dilute polymer solutions increases relative to that of distilled water in the low Reynolds number range. The increased flow rate ratio is a maximum of about 15% in the case of d = 251.8 μm. For the result of the micro PIV measurement, however, there are few differences between the velocity profile of distilled water and the Peo 5 ppm solution.

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Ogata, Satoshi, Kohei Sakai, Kensuke Kanda, and Ming Yang. "Velocity Field Measurements in a Near-Wall Flow of Drag Reducing Solution in Microchannel." In ASME 2006 International Mechanical Engineering Congress and Exposition. ASMEDC, 2006. http://dx.doi.org/10.1115/imece2006-13448.

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The velocity profile of a dilute polymer solution and a surfactant solution near the wall surface in a microchannel was clarified using evanescent wave illumination and a particle tracking velocimetry system. Fluorescent particles with a diameter of 100 nm were used as tracer particles. The test fluids were polyethylene-oxide (Peo15) solution at 5 ppm, oleyl-bihydroxyethyl methyl ammonium chloride (Ethoquad O/12) solution at 200 ppm and distilled water. The results obtained for the velocity profiles for distilled water and surfactant solution were found to agree well with the two-dimensional Poiseuille velocity profile. On the other hand, the velocity profile of the dilute polymer solution decreases significantly compared with that of water within 200 nm of the wall surface. These data provide the first velocity profile measurements of a dilute polymer solution and a surfactant solution in the near-wall region.

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Bertola, V., E. Cafaro, C. Cima, and A. Testa. "Cooling properties of a dilute aqueous polymeric solution." In 40th AIAA Aerospace Sciences Meeting & Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2002. http://dx.doi.org/10.2514/6.2002-497.

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Zhang, Xin, Xili Duan, Yuri Muzychka, and Zongming Wang. "Predicting Drag Reduction in Turbulent Pipe Flow With Relaxation Time of Polymer Additives." In 2018 12th International Pipeline Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/ipc2018-78701.

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This paper presents an experimental study on drag reduction induced by PEO (Polyethylene oxide) in a fully turbulent pipe flow. The objective of this work is to develop a correlation to predict drag reduction using the relaxation time of the polymer additives under dilute solution conditions, i.e., the polymer concentration is less than the overlap concertation. This paper discusses the meaning of relaxation time of polymers, and why the Weissenberg number, a dimensionless number that is related to the relaxation time and shear rate, is independent on the concentration in the dilute solution. Experimental data of drag reduction in a pipe flow are obtained from measurements using a flow loop. A correlation to predict drag reduction with the Weissenberg number and polymer concentration is established and a good agreement is shown between the predicted values and experimental data. The new correlation using the Weissenberg number and polymer concentration is shown to cost less to develop than one using the Reynolds number, in which larger pipes or higher flow rates are required.

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Bertola, Volfango, and Chetan Lakhanpal. "Dilute polymer solution drops impacting on heated surfaces: New impact morphologies and impact regime maps." In ILASS2017 - 28th European Conference on Liquid Atomization and Spray Systems. Valencia: Universitat Politècnica València, 2017. http://dx.doi.org/10.4995/ilass2017.2017.6905.

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The impact morphology of dilute polymer solution drops on a heated surface is studied experimentally by meansof high-speed imaging, with respect to the following parameters: surface temperature; impact Weber number; polymer concentration; polymer molecular weight. In addition to impact morphologies observed in Newtonian drops (deposition, rebound, secondary atomisation and breakup/splashing), three new impact regimes have been identified: (i) a single satellite droplet ejected in the direction of bouncing but tethered to the main drop by a thin liquid filament; (ii) a splashing-like behaviour (semi-splashing), where the rim instability generates satellite droplets tethered to the lamella by thin liquid filaments; (iii) a spray-like behaviour (semi-spray), where a fine secondary atomisation generated upon impact is quickly absorbed back into the drop globule. Experiments were carried out using drops of aqueous polyethylene oxide (PEO) solutions, with mass concentrations of 100 ppm, 200 ppm and 400 ppm, and PEO molecular weights of 2 MDa, 4MDa, and 8MDa. The impact morphology on a polished aluminium surface with temperatures ranging between 160°C and 400°C was investigated for impact Weber numbers between 20 and 170, taking side view images of impacting drops at a rate of 1,000 frames persecond.DOI: http://dx.doi.org/10.4995/ILASS2017.2017.4905

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Reports on the topic "Polymer in dilute solution"

1

Braun, B., W. Blanch, and J. M. Prausnitz. Capillary electrophoretic separation of DNA restriction fragments using dilute polymer solutions. Office of Scientific and Technical Information (OSTI), February 1997. http://dx.doi.org/10.2172/453768.

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Curro, John G., and Amalie Lucile Frischknecht. Solution behavior of PEO : the ultimate biocompatible polymer. Office of Scientific and Technical Information (OSTI), November 2004. http://dx.doi.org/10.2172/958378.

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Cotts, P. M., R. D. Miller, and R. Sooriyakumaran. Configurational Properties of a Stiff-Chain Diaryl Substituted Polysilane in Dilute Solution. Fort Belvoir, VA: Defense Technical Information Center, August 1988. http://dx.doi.org/10.21236/ada198412.

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Gdowski, G. Formulation and make-up of simulate dilute water, low ionic content aqueous solution. Office of Scientific and Technical Information (OSTI), April 1997. http://dx.doi.org/10.2172/2807.

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Anderson, Joshua Allen. Phases of polymer systems in solution studied via molecular dynamics. Office of Scientific and Technical Information (OSTI), May 2009. http://dx.doi.org/10.2172/1342562.

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Madras, G., J. M. Smith, and B. J. McCoy. Effect of tetralin on the degradation of polymer in solution. Office of Scientific and Technical Information (OSTI), December 1995. http://dx.doi.org/10.2172/207369.

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Hong, Seok H., and Wendel J. Shuely. Influence of Trace Components on the Viscoelastic Properties of a Polymer Solution. Fort Belvoir, VA: Defense Technical Information Center, August 1993. http://dx.doi.org/10.21236/ada277171.

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Madras, G., J. M. Smith, and B. J. McCoy. Effect of tetralin on polymer degradation in solution. [Quarterly report, January--March 1995]. Office of Scientific and Technical Information (OSTI), April 1995. http://dx.doi.org/10.2172/100276.

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Leveillee, S. Y. The corrosion effect of ozonated seawater solution on titanium in polymer generated crevice environments. Office of Scientific and Technical Information (OSTI), January 1998. http://dx.doi.org/10.2172/329560.

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Yang, Yang. Integrated Instrumentation System for the Characterization of Polymer Solution and Gel-Light-Emitting Devices. Fort Belvoir, VA: Defense Technical Information Center, March 2001. http://dx.doi.org/10.21236/ada387981.

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