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Sample records for branched polymers polymer

  1. Melons are branched polymers

    CERN Document Server

    Gurau, Razvan

    2013-01-01

    Melonic graphs constitute the family of graphs arising at leading order in the 1/N expansion of tensor models. They were shown to lead to a continuum phase, reminiscent of branched polymers. We show here that they are in fact precisely branched polymers, that is, they possess Hausdorff dimension 2 and spectral dimension 4/3.

  2. Size-exclusion chromatography (SEC) of branched polymers and polysaccharides

    OpenAIRE

    Gaborieau, Marianne; Castignolles, Patrice

    2010-01-01

    Branched polymers are among the most important polymers, ranging from polyolefins to polysaccharides. Branching plays a key role in the chain dynamics. It is thus very important for application properties such as mechanical and adhesive properties and digestibility. It also plays a key role in viscous properties, and thus in the mechanism of the separation of these polymers in size-exclusion chromatography (SEC). Critically reviewing the literature, particularly on SEC of polyolefins, polyacr...

  3. Branched Polymers via ROMP of Termimers.

    Science.gov (United States)

    Hanik, Nils; Kilbinger, Andreas F M

    2016-03-01

    Today's olefin metathesis catalysts show high reactivity, selectivity, and functional group tolerance and allow the design of new syntheses of precisely functionalized polymers. Here the synthesis of a new end-capping reagent is investigated allowing the introduction of a highly reactive activated ester end-group at the polymer chain end as well as its prefunctionalization to directly introduce functional moieties. The versatility of this new end-capping reagent is demonstrated by utilizing it to synthesize a so-called termimer (a monomer with termination capabilities). Copolymerization of a norbornene derivative with the termimer leads to hyperbranched ring-opening metathesis polymerization polymers as proven by gel permeation chromatography and MALDI-ToF-(matrix-assisted laser desorption/ionization time of flight) mass spectrometry. PMID:26787265

  4. The Spectral Dimension of Non-generic Branched Polymer Ensembles

    CERN Document Server

    Correia, J D; Correia, Joao D.; Wheater, John F.

    1998-01-01

    We show that the spectral dimension on non-generic branched polymer models with susceptibility exponent $\\gamma$ is given by $2/(1+\\gamma)$. For those models with negative $\\gamma$ we find that the spectral dimension is 2.

  5. Size-exclusion chromatography (SEC) of branched polymers and polysaccharides.

    Science.gov (United States)

    Gaborieau, Marianne; Castignolles, Patrice

    2011-02-01

    Branched polymers are among the most important polymers, ranging from polyolefins to polysaccharides. Branching plays a key role in the chain dynamics. It is thus very important for application properties such as mechanical and adhesive properties and digestibility. It also plays a key role in viscous properties, and thus in the mechanism of the separation of these polymers in size-exclusion chromatography (SEC). Critically reviewing the literature, particularly on SEC of polyolefins, polyacrylates and starch, we discuss common pitfalls but also highlight some unexplored possibilities to characterize branched polymers. The presence of a few long-chain branches has been shown to lead to a poor separation in SEC, as evidenced by multiple-detection SEC or multidimensional liquid chromatography. The local dispersity can be large in that case, and the accuracy of molecular weight determination achieved by current methods is poor, although hydrodynamic volume distributions offer alternatives. In contrast, highly branched polymers do not suffer from this extensive incomplete separation in terms of molecular weight. PMID:20967430

  6. The effect of branching in a semiconducting polymer on the efficiency of organic photovoltaic cells.

    Science.gov (United States)

    Heintges, Gaël H L; van Franeker, Jacobus J; Wienk, Martijn M; Janssen, René A J

    2016-01-01

    The impact of branching in a diketopyrrolopyrrole polymer on the performance of polymer-fullerene photovoltaic cells is investigated. Compared to the linear polymer, the branched polymer affords a more finely dispersed fibrillar network in the photoactive layer and as a result a large enhancement of the photocurrent and power conversion efficiency.

  7. From chromosome crumpling to the interacting randomly branched polymers

    Science.gov (United States)

    Everaers, Ralf

    The conformational statistics of ring polymers in melts or dense solutions is strongly affected by their quenched microscopic topological state. The effect is particularly strong for non-concatenated unknotted rings, which are known to crumple and segregate and which have been implicated as models for the generic behavior of interphase chromosomes. In we have used a computationally efficient multi-scale approach to identify the subtle physics underlying their behavior, where we combine massive Molecular Dynamics simulations on the fiber level with Monte Carlo simulations of a wide range of lattice models for the large scale structure. This allowed us to show that ring melts can be quantitatively mapped to coarse-grained melts of interacting randomly branched primitive paths. To elucidate the behavior of interacting branched polymers, we use a combination of scaling arguments and computer simulations. The simulations are carried out for different statistical ensembles: ideal randomly branching polymers, melts of interacting randomly branching polymers, and self-avoiding trees with annealed and quenched connectivities. In all cases, we perform a detailed analysis of the tree connectivities and conformations. We find that the scaling behaviour of average properties is very well described by the Flory theory of Gutin et al. [Macromolecules 26, 1293 (1993)]. A detailed study of the corresponding distribution functions allows us to propose a coherent framework of the behavior of interacting trees, including generalised Fisher-Pincus relationships and the detailed analysis of contacts statistics.

  8. Branched polymers, complex spins and the freezing transition

    CERN Document Server

    Correia, J D; Wheater, John F; Correia, Joao D.; Mirza, Behrouz; Wheater, John F.

    1997-01-01

    We show that by coupling complex three-state systems to branched-polymer like ensembles we can obtain models with gamma-string different from one half. It is also possible to study the interpolation between dynamical and crystalline graphs for these models; we find that only when geometry fluctuations are completely forbidden is there a crystalline phase.

  9. Fractal Dimension of Randomly Branched Polymers in a Good Solvent

    Institute of Scientific and Technical Information of China (English)

    巴信武; 张书文; 王海军; 王素娟; 韩颖慧

    2002-01-01

    We propose a concept of subchains for randomly branched polymers. As a direct application of this concept,the asymptotic expression of the average mean square radius of gyration is determined to give the fractal dimensions, in which the excluded volume effect is taken into consideration. Furthermore, we investigate a scaling relation that is associated with the Flory exponent v, the fractal dimension df and the polydispersity exponent τ.

  10. Communication: When does a branched polymer become a particle?

    Science.gov (United States)

    Chremos, Alexandros; Douglas, Jack F

    2015-09-21

    Polymer melts with topologically distinct molecular structures, namely, linear chain, ring, and star polymers, are investigated by molecular dynamics simulation. In particular, we determine the mean polymer size and shape, and glass transition temperature for each molecular topology. Both in terms of structure and dynamics, unknotted ring polymers behave similarly to star polymers with f ≈ 5-6 star arms, close to a configurational transition point between anisotropic chains to spherically symmetric particle-like structures. These counter-intuitive findings raise fundamental questions regarding the importance of free chain-ends and chain topology in the packing and dynamics of polymeric materials. PMID:26395679

  11. The spectral dimension of the branched polymers phase of two-dimensional quantum gravity

    CERN Document Server

    Jónsson, T; Jonsson, Thordur; Wheater, John F.

    1998-01-01

    The metric of two-dimensional quantum gravity interacting with conformal matter is believed to collapse to a branched polymer metric when the central charge c>1. We show analytically that the spectral dimension of such a branched polymer phase is four thirds. This is in good agreement with numerical simulations for large c.

  12. Diketopyrrolopyrrole-based Conjugated Polymers Bearing Branched Oligo(Ethylene Glycol) Side Chains for Photovoltaic Devices.

    Science.gov (United States)

    Chen, Xingxing; Zhang, Zijian; Ding, Zicheng; Liu, Jun; Wang, Lixiang

    2016-08-22

    Conjugated polymers are essential for solution-processable organic opto-electronic devices. In contrast to the great efforts on developing new conjugated polymer backbones, research on developing side chains is rare. Herein, we report branched oligo(ethylene glycol) (OEG) as side chains of conjugated polymers. Compared with typical alkyl side chains, branched OEG side chains endowed the resulting conjugated polymers with a smaller π-π stacking distance, higher hole mobility, smaller optical band gap, higher dielectric constant, and larger surface energy. Moreover, the conjugated polymers with branched OEG side chains exhibited outstanding photovoltaic performance in polymer solar cells. A power conversion efficiency of 5.37 % with near-infrared photoresponse was demonstrated and the device performance could be insensitive to the active layer thickness.

  13. Synthesis and characterization of a hyper-branched water-soluble β-cyclodextrin polymer

    OpenAIRE

    Francesco Trotta; Fabrizio Caldera; Roberta Cavalli; Andrea Mele; Carlo Punta; Lucio Melone; Franca Castiglione; Barbara Rossi (Duke); Monica Ferro; Vincenza Crupi; Domenico Majolino; Valentina Venuti; Dominique Scalarone

    2014-01-01

    A new hyper-branched water-soluble polymer was synthesized by reacting β-cyclodextrin with pyromellitic dianhydride beyond the critical conditions that allow the phenomenon of gelation to occur. The molar ratio between the monomers is a crucial parameter that rules the gelation process. Nevertheless, the concentration of monomers in the solvent phase plays a key role as well. Hyper-branched β-cyclodextrin-based polymers were obtained performing the syntheses with excess of solvent and cross-l...

  14. Computer simulations of randomly branching polymers: annealed versus quenched branching structures

    Science.gov (United States)

    Rosa, Angelo; Everaers, Ralf

    2016-08-01

    We present computer simulations of three systems of randomly branching polymers in d = 3 dimensions: ideal trees and self-avoiding trees with annealed and quenched connectivities. In all cases, we performed a detailed analysis of trees connectivities, spatial conformations and statistical properties of linear paths on trees, and compare the results to the corresponding predictions of Flory theory. We confirm that, overall, the theory predicts correctly that trees with quenched ideal connectivity exhibit less overall swelling in good solvent than corresponding trees with annealed connectivity even though they are more strongly stretched on the path level. At the same time, we emphasize the inadequacy of the Flory theory in predicting the behaviour of other, and equally relevant, observables like contact probabilities between tree nodes. We show, then, that contact probabilities can be aptly characterized by introducing a novel critical exponent, {θ }{path}, which accounts for how they decay as a function of the node-to-node path distance on the tree.

  15. Disorder effects on the static scattering function of star branched polymers

    Directory of Open Access Journals (Sweden)

    V. Blavatska

    2012-10-01

    Full Text Available We present an analysis of the impact of structural disorder on the static scattering function of f-armed star branched polymers in d dimensions. To this end, we consider the model of a star polymer immersed in a good solvent in the presence of structural defects, correlated at large distances r according to a power law ~r-a. In particular, we are interested in the ratio g(f of the radii of gyration of star and linear polymers of the same molecular weight, which is a universal experimentally measurable quantity. We apply a direct polymer renormalization approach and evaluate the results within the double ϵ = 4 - d, δ = 4 - a-expansion. We find an increase of g(f with an increasing δ. Therefore, an increase of disorder correlations leads to an increase of the size measure of a star relative to linear polymers of the same molecular weight.

  16. Communication: Role of short chain branching in polymer structure and dynamics

    Science.gov (United States)

    Kim, Jun Mo; Baig, Chunggi

    2016-02-01

    A comprehensive understanding of chain-branching effects, essential for establishing general knowledge of the structure-property-phenomenon relationship in polymer science, has not yet been found, due to a critical lack of knowledge on the role of short-chain branches, the effects of which have mostly been neglected in favor of the standard entropic-based concepts of long polymers. Here, we show a significant effect of short-chain branching on the structural and dynamical properties of polymeric materials, and reveal the molecular origins behind the fundamental role of short branches, via atomistic nonequilibrium molecular dynamics and mesoscopic Brownian dynamics by systematically varying the strength of the mobility of short branches. We demonstrate that the fast random Brownian kinetics inherent to short branches plays a key role in governing the overall structure and dynamics of polymers, leading to a compact molecular structure and, under external fields, to a lesser degree of structural deformation of polymer, to a reduced shear-thinning behavior, and to a smaller elastic stress, compared with their linear analogues. Their fast dynamical nature being unaffected by practical flow fields owing to their very short characteristic time scale, short branches would substantially influence (i.e., facilitate) the overall relaxation behavior of polymeric materials under various flowing conditions.

  17. Beyond branching: multiknot structured polymer for gene delivery.

    Science.gov (United States)

    Aied, Ahmed; Zheng, Yu; Newland, Ben; Wang, Wenxin

    2014-12-01

    Polymer-based transfection vectors are increasingly becoming the preferred alternative to viral vectors thanks to their safety and ease of production, but low transfection potency has limited their application. Many polycationic vectors show high efficiency in vitro, but their excessive charge density makes them toxic for in vivo applications. Herein, we demonstrate the synthesis of new and unique disulfide-reducible polymeric gene nanocarriers that exhibit significantly enhanced transfection potency and low cytotoxicity, particularly in skin cells, surpassing the efficiency of the well-known transfection reagents polyethylenimine (PEI) and Lipofectamine2000. The unique three-dimensional (3D) "multiknot" vectors were synthesized from in situ deactivation enhanced atom transfer radical (co)polymerization (DE-ATRP) of multivinyl monomers (MVMs). The high transfection levels and low toxicity of this multiknot structured polymer in vitro, combined with its ability to mediate collagen VII expression in 3D skin equivalents made from cells of recessive dystrophic epidermolysis bullosa patients, demonstrates its use as a platform nanotechnology which should be investigated further for dermatological disease therapies. Our findings suggest that the marked improvements stem from the dense multiknot architecture and degradable property, which facilitate both the binding and releasing process of the plasmid DNA. PMID:25375252

  18. Synthesis and characterization of a hyper-branched water-soluble β-cyclodextrin polymer

    Directory of Open Access Journals (Sweden)

    Francesco Trotta

    2014-11-01

    Full Text Available A new hyper-branched water-soluble polymer was synthesized by reacting β-cyclodextrin with pyromellitic dianhydride beyond the critical conditions that allow the phenomenon of gelation to occur. The molar ratio between the monomers is a crucial parameter that rules the gelation process. Nevertheless, the concentration of monomers in the solvent phase plays a key role as well. Hyper-branched β-cyclodextrin-based polymers were obtained performing the syntheses with excess of solvent and cross-linking agent, and the conditions for critical dilution were determined experimentally. A hyper-branched polymer with very high water solubility was obtained and fully characterized both as for its chemical structure and for its capability to encapsulate substances. Fluorescein was used as probe molecule to test the complexation properties of the new material.

  19. Mean span dimensions of ideal polymer chains containing branches and rings

    DEFF Research Database (Denmark)

    Wang, Yanwei; Teraoka, Iwao; Hansen, Flemming Yssing;

    2011-01-01

    We present a general method for calculating the mean span dimension of various branched and ringed polymers under the assumption of Gaussian chain statistics. The method allows a routine construction of an integral expression of the mean span dimension based on three base functions, determined...... for a connector, an arm and a loop, respectively. Applications of our method are shown to a variety of polymer architectures including star, two-branch-point, comb and various cyclic chains (eight-shaped, θ-shaped and several semicyclic chains). Comparing the mean span dimension with other commonly used molecular...

  20. Using 2D NMR to determine the degree of branching of complicated hyperbranched polymers

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Degree of branching (DB) is a crucial structure parameter of hyperbranched polymers, which can be determined by 1H NMR, quantitative 13C NMR, degradative method, etc. However, for complicated hy-perbranched polymers, intricate structure and severe overlap of spectral signals hinder the determina-tion of DB using traditional methods. In this work, the architecture of complicated hyperbranched polymers has been elucidated with the help of 2D NMR techniques. Using such a method, overlapped NMR signals can be well separated into a two-dimensional space, and additional structural information is also available. Correspondingly, quantitative analysis for complicated systems can be realized. De-termination of DBs for three types of complicated hyperbranched polymers synthesized from step-polymerization, self-condensation vinyl polymerization and self-condensation ring-opening po-lymerization is shown as examples.

  1. Perspectives on the viscoelasticity and flow behavior of entangled linear and branched polymers

    International Nuclear Information System (INIS)

    We briefly review the recent advances in the rheology of entangled polymers and identify emerging research trends and outstanding challenges, especially with respect to branched polymers. Emphasis is placed on the role of well-characterized model systems, as well as the synergy of synthesis-characterization, rheometry and modeling/simulations. The theoretical framework for understanding the observed linear and nonlinear rheological phenomena is the tube model, which is critically assessed in view of its successes and shortcomings, and alternative approaches are briefly discussed. Finally, intriguing experimental findings and controversial issues that merit consistent explanation, such as shear banding instabilities, multiple stress overshoots in transient simple shear and enhanced steady-state elongational viscosity in polymer solutions, are discussed, and future directions such as branch point dynamics and anisotropic monomeric friction are outlined. (topical review)

  2. Creep measurements confirm steady flow after stress maximum in extension of branched polymer melts

    DEFF Research Database (Denmark)

    Javier Alvarez, Nicolas; Román Marín, José Manuel; Huang, Qian;

    2013-01-01

    We provide conclusive evidence of nonmonotonic mechanical behavior in the extension of long-chain branched polymer melts. While nonmonotonic behavior is known to occur for solids, for the case of polymeric melts, this phenomenon is in direct contrast with current theoretical models. We rule out t...

  3. The local free volume and its correlation with the structural, chemical and dynamic properties of branched polymers, polymer electrolytes, highly oriented polyethylene fibres and other polymers

    CERN Document Server

    Bamford, D

    2002-01-01

    The work described in this thesis is concerned with the study of the local free volume measured by Positron Annihilation Spectroscopy and its correlation with the physical, chemical and structural properties of polymers. The average size of the local free volume holes in branched poly(ethylene-co-olefin) and poly(propylene-co-olefin) copolymers is studied using Positron Annihilation Lifetime Spectroscopy PALS and correlated with the number and length of the branches and the physical properties determined from Differential Scanning Calorimetry DSC and density measurements. The presence of the n-alkyl branches were found to form sterical hindrances to an effective chain packing resulting in a linear increase in the average free volume hole sizes, an increase in the specific volume of the amorphous phase, a decrease in the sample crystallinity and a decrease in the glass transition and melting temperatures. A linear relation was found between the average size of the free volume holes and the glass transition tem...

  4. DEGREE OF BRANCHING OF THE HYPERBRANCHED POLYMERS RESULTED FROM AB2 POLYCONDENSATION WITH SUBSTITUTION EFFECT

    Institute of Scientific and Technical Information of China (English)

    Zhi-ping Zhou; De-yue Yan

    2011-01-01

    The analytical expressions of the various structural units and the average degree of branching for the hyperbranched polymers resulted from AB2 polycondensation with substitution effect were derived by the kinetic mechanism.The reactivity difference between the B group in linear unit and that in terminal group has great effect on the molecular parameters of the products obtained.The concentration of terminal units has a maximum with the increase of the conversion of A groups (x).The higher the reactivity ratio (r) of linear B group to branched one is,the later the maximum appears and the larger it is.The degree of branching of the hyperbranched polymers obtained is controllable by adjusting the parameters ofr andx,which increases with increasing both x and r.

  5. Ampicillin-Ester Bonded Branched Polymers: Characterization, Cyto-, Genotoxicity and Controlled Drug-Release Behaviour

    Directory of Open Access Journals (Sweden)

    Ewa Oledzka

    2014-06-01

    Full Text Available The development and characterization of novel macromolecular conjugates of ampicillin using branched biodegradable polymers has been described in this study. The conjugates have been prepared coupling the β-lactam antibiotic with branched polymer matrices based on the natural oligopeptide core. The cyto- and genotoxicity of the synthesized polymers were evaluated with a bacterial luminescence test, two protozoan assays and Salmonella typhimurium TA1535. The presence of a newly formed covalent bond between the drug and the polymer matrices was confirmed by 1H-NMR and FTIR studies. A drug content (15.6 and 10.2 mole % in the macromolecular conjugates has been determined. The obtained macromolecular products have been subjected to further in vitro release studies. The total percentage of ampicillin released after 21 days of incubation was nearly 60% and 14% and this resulted from the different physicochemical properties of the polymeric matrices. This is the first report on the application of branched biodegradable polymeric matrices for the covalent conjugation of ampicillin. The obtained results showed that the synthesized macromolecular drug-conjugates might slowly release the active drug molecule and improve the pharmacokinetics of ampicillin.

  6. Separation of complex branched polymers by size-exclusion chromatography probed with multiple detection.

    Science.gov (United States)

    Gaborieau, Marianne; Nicolas, Julien; Save, Maud; Charleux, Bernadette; Vairon, Jean-Pierre; Gilbert, Robert G; Castignolles, Patrice

    2008-05-01

    Size-exclusion chromatography (SEC) separates polymers by hydrodynamic volume (the universal calibration principle). Molecular weights can be determined using viscometry (relying on universal calibration) and light scattering (independent of universal calibration). In the case of complex branched polyacrylates with tetrahydrofuran as eluent, universal calibration is valid, although the separation in term of molecular weight is incomplete: a given elution slice contains a range of molecular weights, described in terms of a 'local polydispersity'. The local polydispersity index decreases when the number of branches per chain increases and complete separation is reached for highly branched chains. PMID:18378255

  7. Polymer films

    Science.gov (United States)

    Granick, Steve; Sukhishvili, Svetlana A.

    2008-12-30

    A film contains a first polymer having a plurality of hydrogen bond donating moieties, and a second polymer having a plurality of hydrogen bond accepting moieties. The second polymer is hydrogen bonded to the first polymer.

  8. Proposed sets of critical exponents for randomly branched polymers, using a known string theory model

    Science.gov (United States)

    March, N. H.; Moreno, A. J.

    2016-06-01

    The critical exponent ν for randomly branched polymers with dimensionality d equal to 3, is known exactly as 1/2. Here, we invoke an already available string theory model to predict the remaining static critical exponents. Utilizing results of Hsu et al. (Comput Phys Commun. 2005;169:114-116), results are added for d = 8. Experiment plus simulation would now be important to confirm, or if necessary to refine, the proposed values.

  9. Three-State Complex Valued Spins Coupled to Binary Branched Polymers in Two-Dimensional Quantum Gravity

    CERN Document Server

    Correia, J D; Correia, Joao D.; Wheater, John F.

    1998-01-01

    A model of complex spins (corresponding to a non-minimal model in the language of CFT) coupled to the binary branched polymer sector of quantum gravity is considered. We show that this leads to new behaviour.

  10. Polymer fractionation

    Energy Technology Data Exchange (ETDEWEB)

    Hadermann, A. F.

    1985-04-09

    Soluble polymers are fractionated according to molecular weight by cryogenically comminuting the polymer and introducing the polymer particles, while still in the active state induced by cryogenic grinding, into a liquid having a solvent power selected to produce a coacervate fraction containing high molecular weight polymer species and a dilute polymer solution containing lower molecular weight polymer species. The coacervate may be physically separated from the solution and finds use in the production of antimisting jet fuels and the like.

  11. Searching for low percolation thresholds within amphiphilic polymer membranes: The effect of side chain branching

    Science.gov (United States)

    Dorenbos, G.

    2015-06-01

    Percolation thresholds for solvent diffusion within hydrated model polymeric membranes are derived from dissipative particle dynamics in combination with Monte Carlo (MC) tracer diffusion calculations. The polymer backbones are composed of hydrophobic A beads to which at regular intervals Y-shaped side chains are attached. Each side chain is composed of eight A beads and contains two identical branches that are each terminated with a pendant hydrophilic C bead. Four types of side chains are considered for which the two branches (each represented as [C], [AC], [AAC], or [AAAC]) are splitting off from the 8th, 6th, 4th, or 2nd A bead, respectively. Water diffusion through the phase separated water containing pore networks is deduced from MC tracer diffusion calculations. The percolation threshold for the architectures containing the [C] and [AC] branches is at a water volume fraction of ˜0.07 and 0.08, respectively. These are much lower than those derived earlier for linear architectures of various side chain length and side chain distributions. Control of side chain architecture is thus a very interesting design parameter to decrease the percolation threshold for solvent and proton transports within flexible amphiphilic polymer membranes.

  12. Searching for low percolation thresholds within amphiphilic polymer membranes: The effect of side chain branching

    Energy Technology Data Exchange (ETDEWEB)

    Dorenbos, G., E-mail: dorenbos@ny.thn.ne.jp [Sano 1107-2, Belle Crea 502, Susono 410-1118 (Japan)

    2015-06-14

    Percolation thresholds for solvent diffusion within hydrated model polymeric membranes are derived from dissipative particle dynamics in combination with Monte Carlo (MC) tracer diffusion calculations. The polymer backbones are composed of hydrophobic A beads to which at regular intervals Y-shaped side chains are attached. Each side chain is composed of eight A beads and contains two identical branches that are each terminated with a pendant hydrophilic C bead. Four types of side chains are considered for which the two branches (each represented as [C], [AC], [AAC], or [AAAC]) are splitting off from the 8th, 6th, 4th, or 2nd A bead, respectively. Water diffusion through the phase separated water containing pore networks is deduced from MC tracer diffusion calculations. The percolation threshold for the architectures containing the [C] and [AC] branches is at a water volume fraction of ∼0.07 and 0.08, respectively. These are much lower than those derived earlier for linear architectures of various side chain length and side chain distributions. Control of side chain architecture is thus a very interesting design parameter to decrease the percolation threshold for solvent and proton transports within flexible amphiphilic polymer membranes.

  13. Creep measurements confirm steady flow after stress maximum in extension of branched polymer melts

    DEFF Research Database (Denmark)

    Javier Alvarez, Nicolas; Román Marín, José Manuel; Huang, Qian;

    2013-01-01

    We provide conclusive evidence of nonmonotonic mechanical behavior in the extension of long-chain branched polymer melts. While nonmonotonic behavior is known to occur for solids, for the case of polymeric melts, this phenomenon is in direct contrast with current theoretical models. We rule out...... the possibility of the overshoot being an experimental artifact by confirming the existence of steady flow after a maximum in the ratio of stress to strain rate versus strain under both constant stress and constant strain-rate kinematics. This observation indicates the omission of important physics from current...

  14. Biodegradable Polymers

    Directory of Open Access Journals (Sweden)

    Isabelle Vroman

    2009-04-01

    Full Text Available Biodegradable materials are used in packaging, agriculture, medicine and other areas. In recent years there has been an increase in interest in biodegradable polymers. Two classes of biodegradable polymers can be distinguished: synthetic or natural polymers. There are polymers produced from feedstocks derived either from petroleum resources (non renewable resources or from biological resources (renewable resources. In general natural polymers offer fewer advantages than synthetic polymers. The following review presents an overview of the different biodegradable polymers that are currently being used and their properties, as well as new developments in their synthesis and applications.

  15. Polymer electronics

    CERN Document Server

    Hsin-Fei, Meng

    2013-01-01

    Polymer semiconductor is the only semiconductor that can be processed in solution. Electronics made by these flexible materials have many advantages such as large-area solution process, low cost, and high performance. Researchers and companies are increasingly dedicating time and money in polymer electronics. This book focuses on the fundamental materials and device physics of polymer electronics. It describes polymer light-emitting diodes, polymer field-effect transistors, organic vertical transistors, polymer solar cells, and many applications based on polymer electronics. The book also disc

  16. Branched polymers characterized by comprehensive two-dimensional separations with fully orthogonal mechanisms: Molecular-topology fractionation x size-exclusion chromatography

    NARCIS (Netherlands)

    R. Edam; E.P.C. Mes; D.M. Meunier; F.A. van Damme; P.J. Schoenmakers

    2014-01-01

    Polymer separations under non-conventional conditions have been explored to obtain a separation of long-chain branched polymers from linear polymers with identical hydrodynamic size. In separation media with flow-through channels of the same order as the size of the analyte molecules in solution, th

  17. Solid Polymer Electrolytes Based on Cross-linkable Oligo (oxyethylene)-Branched Oligo (organophosphazenes)

    Institute of Scientific and Technical Information of China (English)

    Shuhua Zhou; Shibi Fang

    2005-01-01

    @@ 1Introduction Solid polymer electrolytes have attracted considerable interest because of their potential application in secondary high energy density lithium batteries. The poly(ethylene oxide)(PEO) has been widely studied as the classical polymer matrix for solid polymer electrolytes. However, the poor room temperature conductivity due to its crystalline is the principal problem to be overcomed. This has prompted many researchers to attempt to modify the properties of PEO.

  18. Photoaddressable Polymers

    Science.gov (United States)

    Bieringer, T.

    Polymers are the perfect materials for a variety of applications in almost every field of technical as well as human life. Because of their macromolecular architecture there are a lot of degrees of freedom in the synthesis of polymers. Owing to the change of their functional composition, they can be tailored even for quite difficult demands. Since a whole industry deals with the processing of polymers, cheap production lines have been developed for almost every polymer. This is the reason why not only the molecular composition but even the price of polymers has been optimized. Therefore these materials can be considered as encouraging components even in highly sophisticated areas of applications.

  19. Fluorocarbon Surfactant Polymers: Effect of Perfluorocarbon Branch Density on Surface Active Properties

    OpenAIRE

    WANG, SHUWU; Marchant, Roger E.

    2004-01-01

    We describe a series of fluorocarbon surfactant polymers designed for modifying fluorocarbon surfaces such as poly(tetrafluoroethylene). Novel fluorocarbon surfactant polymers poly(N-vinyldextranaldonamide-co-N-vinylperfluoroundecanamide), in which hydrophilic dextran oligosaccharides and hydrophobic perfluoroundecanoyl groups were incorporated sequentially onto a poly(vinylamine) backbone, were synthesized and characterized by FT-IR, NMR, and XPS spectroscopy. By adjusting the feed ratio of ...

  20. Branched Polymers and their Application in Corrosion Inhibition for mild steel in 1M H2SO4 medium

    Directory of Open Access Journals (Sweden)

    Sounthari. P

    2014-12-01

    Full Text Available The adsorption and corrosion inhibiting effect of branched polymers (BATP, BAAZ, BETP & BEAZ on mild steel in 1M H2SO4 at 30±1˚C was investigated using gravimetric, electrochemical impedance spectroscopy (EIS, and potentiodynamic polarization techniques. The experimental findings revealed that BATP inhibited the corrosion reaction in the acid environment to greater extend compared to BAAZ, BETP and BEAZ. Impedance results indicate that the polymers were adsorbed on the metal/solution interface, while polarization data showed that the polymers behaved mostly as mixed-type inhibitors. Kinetic parameters (activation energy, pre-exponential factor, enthalpy of activation and entropy of activation as well as thermodynamic parameters (enthalpy of adsorption, entropy of adsorption and Gibbs free energy were calculated and discussed. Scanning electron microscopy technique was used to confirm the effectiveness of inhibition of mild steel in sulphuric acid medium.

  1. Polymer Chemistry

    Science.gov (United States)

    Williams, Martha; Roberson, Luke; Caraccio, Anne

    2010-01-01

    This viewgraph presentation describes new technologies in polymer and material chemistry that benefits NASA programs and missions. The topics include: 1) What are Polymers?; 2) History of Polymer Chemistry; 3) Composites/Materials Development at KSC; 4) Why Wiring; 5) Next Generation Wiring Materials; 6) Wire System Materials and Integration; 7) Self-Healing Wire Repair; 8) Smart Wiring Summary; 9) Fire and Polymers; 10) Aerogel Technology; 11) Aerogel Composites; 12) Aerogels for Oil Remediation; 13) KSC's Solution; 14) Chemochromic Hydrogen Sensors; 15) STS-130 and 131 Operations; 16) HyperPigment; 17) Antimicrobial Materials; 18) Conductive Inks Formulations for Multiple Applications; and 19) Testing and Processing Equipment.

  2. Polymers & People

    Science.gov (United States)

    Lentz, Linda; Robinson, Thomas; Martin, Elizabeth; Miller, Mary; Ashburn, Norma

    2004-01-01

    Each Tuesday during the fall of 2002, teams of high school students from three South Carolina counties conducted a four-hour polymer institute for their peers. In less than two months, over 300 students visited the Charleston County Public Library in Charleston, South Carolina, to explore DNA, nylon, rubber, gluep, and other polymers. Teams of…

  3. Polymer Informatics

    Science.gov (United States)

    Adams, Nico

    Polymers are arguably the most important set of materials in common use. The increasing adoption of both combinatorial as well as high-throughput approaches, coupled with an increasing amount of interdisciplinarity, has wrought tremendous change in the field of polymer science. Yet the informatics tools required to support and further enhance these changes are almost completely absent. In the first part of the chapter, a critical analysis of the challenges facing modern polymer informatics is provided. It is argued, that most of the problems facing the field today are rooted in the current scholarly communication process and the way in which chemists and polymer scientists handle and publish data. Furthermore, the chapter reviews existing modes of representing and communicating polymer information and discusses the impact, which the emergence of semantic technologies will have on the way in which scientific and polymer data is published and transmitted. In the second part, a review of the use of informatics tools for the prediction of polymer properties and in silico design of polymers is offered.

  4. Engineering Polymer Informatics

    OpenAIRE

    Adams, Nico; Ryder, Jennifer; Jessop, David M; Corbett, Peter; Murray-Rust, Peter

    2007-01-01

    The poster describes a strategy of for the development of polymer informatics. In particular, the development of polymer markup language, a polymer ontology and natural language processing tools for polymer literature.

  5. Antimocrobial Polymer

    Energy Technology Data Exchange (ETDEWEB)

    McDonald, William F. (Utica, OH); Huang, Zhi-Heng (Walnut Creek, CA); Wright, Stacy C. (Columbus, GA)

    2005-09-06

    A polymeric composition having antimicrobial properties and a process for rendering the surface of a substrate antimicrobial are disclosed. The composition comprises a crosslinked chemical combination of (i) a polymer having amino group-containing side chains along a backbone forming the polymer, (ii) an antimicrobial agent selected from quaternary ammonium compounds, gentian violet compounds, substituted or unsubstituted phenols, biguanide compounds, iodine compounds, and mixtures thereof, and (iii) a crosslinking agent containing functional groups capable of reacting with the amino groups. In one embodiment, the polymer is a polyamide formed from a maleic anhydride or maleic acid ester monomer and alkylamines thereby producing a polyamide having amino substituted alkyl chains on one side of the polyamide backbone; the crosslinking agent is a phosphine having the general formula (A)3P wherein A is hydroxyalkyl; and the antimicrobial agent is chlorhexidine, dimethylchlorophenol, cetyl pyridinium chloride, gentian violet, triclosan, thymol, iodine, and mixtures thereof.

  6. Antimicrobial Polymer

    Energy Technology Data Exchange (ETDEWEB)

    McDonald, William F. (Utica, OH); Wright, Stacy C. (Flint, MI); Taylor, Andrew C. (Ann Arbor, MI)

    2004-09-28

    A polymeric composition having antimicrobial properties and a process for rendering the surface of a substrate antimicrobial are disclosed. The polymeric composition comprises a crosslinked chemical combination of (i) a polymer having amino group-containing side chains along a backbone forming the polymer, (ii) an antimicrobial agent selected from metals, metal alloys, metal salts, metal complexes and mixtures thereof, and (iii) a crosslinking agent containing functional groups capable of reacting with the amino groups. In one example embodiment, the polymer is a polyamide formed from a maleic anhydride or maleic acid ester monomer and alkylamines thereby producing a polyamide having amino substituted alkyl chains on one side of the polyamide backbone; the crosslinking agent is a phosphine having the general formula (A).sub.3 P wherein A is hydroxyalkyl; and the metallic antimicrobial agent is selected from chelated silver ions, silver metal, chelated copper ions, copper metal, chelated zinc ions, zinc metal and mixtures thereof.

  7. Polymer Materials

    Institute of Scientific and Technical Information of China (English)

    Charles C. Han; DONG Jinyong; NIU Hui; CHENG He; HUANG Ye; ZHENG Jianfen; XU Shanshan

    2011-01-01

    @@ Since the second half of the 20th century, polymer materials have already become an essential part of our daily life.The use of polymeric materials has already exceeded that of metals and ceramics in terms of volume and is intimately connected to our clothing, food, household use, transportation, and medical needs.Meanwhile it also brought some recycle and environmental problems.In the 21 st century, human beings are facing ever increasing challenges on environmental protection, energy shortage, and health-medical problems, which have made even higher demand on polymer materials due to its light weight, flexibility and high functionality.

  8. Polymer electronics

    CERN Document Server

    Geoghegan, Mark

    2013-01-01

    Polymer electronics is the science behind many important new developments in technology, such as the flexible electronic display (e-ink) and many new developments in transistor technology. Solar cells, light-emitting diodes, and transistors are all areas where plastic electronics is likely to, or is already having, a serious impact on our daily lives. With polymer transistors and light-emitting diodes now being commercialised, there is a clear need for a pedagogic text thatdiscusses the subject in a clear and concise fashion suitable for senior undergraduate and graduate students. The content

  9. Polymer Science.

    Science.gov (United States)

    Frank, Curtis W.

    1979-01-01

    Described is a series of four graduate level courses in polymer science, offered or currently in preparation, at Stanford University. Course descriptions and a list of required and recommended texts are included. Detailed course outlines for two of the courses are presented. (BT)

  10. Polymer physics

    CERN Document Server

    Gedde, Ulf W

    1999-01-01

    This book is the result of my teaching efforts during the last ten years at the Royal Institute of Technology. The purpose is to present the subject of polymer physics for undergraduate and graduate students, to focus the fundamental aspects of the subject and to show the link between experiments and theory. The intention is not to present a compilation of the currently available literature on the subject. Very few reference citations have thus been made. Each chapter has essentially the same structure: starling with an introduction, continuing with the actual subject, summarizing the chapter in 30D-500 words, and finally presenting problems and a list of relevant references for the reader. The solutions to the problems presented in Chapters 1-12 are given in Chapter 13. The theme of the book is essentially polymer science, with the exclusion of that part dealing directly with chemical reactions. The fundamentals in polymer science, including some basic polymer chemistry, are presented as an introduction in t...

  11. Hyperbranched Polymer-Based Electrolyte for Lithium Polymer Batteries

    Institute of Scientific and Technical Information of China (English)

    Takahito Itoh

    2005-01-01

    @@ 1Introduction Solid polymer electrolytes have attracted much attention as electrolyte materials for all solid-state recharge able lithium batteries, and poly ( ethylene oxide) ( PEO)-based polymer electrolytes are among the most intensively studied systems[1-3]. Hyperbranched polymers have unique properties such as completely amorphous, highly soluble in common organic solvent and processible because of the highly branched nature[4,5].

  12. Uni-axial Elongational Viscosity of Linear and Branched polymer melts

    DEFF Research Database (Denmark)

    Hassager, Ole; Nielsen, Jens Kromann; Rasmussen, Henrik Koblitz

    2005-01-01

    About 40 years ago interest in the measurement of elongational viscosity of polymer melts started to grow. Here we present measurements of transient (and steady) uni-axial elongational viscosity, using the FSR, of the following melts: Four narrow MMD polystyrene (PS) samples with weight......-average molar mass Mw in the range of 50k to 390k. Three different bi-disperse samples, mixed from the narrow MMD PS. Two low-density polyethylene (LDPE) melts (Lupolen 1840D and 3020D). A steady-state viscosity was kept for 1-2.5 Hencky strain units in all measurements.The measurements on the bi-disperse PS...... melts have demonstrated that both the transient and steady elongational viscosity is quite sensitive to polydispersity. Bi-disperse PS resembles the behaviour of mono-disperse melts only at elongational rates larger then the inverse of maximal time constant of the smallest molecule. As observed in Boger...

  13. Acrylic and metal based Y-branch plastic optical fiber splitter with optical NOA63 polymer waveguide taper region

    Science.gov (United States)

    Ehsan, Abang Annuar; Shaari, Sahbudin; Rahman, Mohd Kamil Abd.

    2011-01-01

    We proposed a simple low-cost acrylic and metal-based Y-branch plastic optical fiber (POF) splitter which utilizes a low cost optical polymer glue NOA63 as the main waveguiding medium at the waveguide taper region. The device is composed of three sections: an input POF waveguide, a middle waveguide taper region and output POF waveguides. A desktop high speed CNC engraver is utilized to produce the mold inserts used for the optical devices. Short POF fibers are inserted into the engraved slots at the input and output ports. UV curable optical polymer glue NOA63 is injected into the waveguide taper region and cured. The assembling is completed when the top plate is positioned to enclose the device structure and connecting screws are secured. Both POF splitters have an average insertion loss of 7.8 dB, coupling ratio of 55: 45 and 57: 43 for the acrylic and metal-based splitters respectively. The devices have excess loss of 4.82 and 4.73 dB for the acrylic and metal-based splitters respectively.

  14. Impedimetric Aptasensor for Ochratoxin A Determination Based on Au Nanoparticles Stabilized with Hyper-Branched Polymer

    Directory of Open Access Journals (Sweden)

    Gennady Evtugyn

    2013-11-01

    Full Text Available An impedimetric aptasensor for ochratoxin A (OTA detection has been developed on the base of a gold electrode covered with a new modifier consisting of electropolymerized Neutral Red and a mixture of Au nanoparticles suspended in the dendrimeric polymer Botlorn H30®. Thiolated aptamer specific to OTA was covalently attached to Au nanoparticles via Au-S bonding. The interaction of the aptamer with OTA induced the conformational switch of the aptamer from linear to guanine quadruplex form followed by consolidation of the surface layer and an increase of the charge transfer resistance. The aptasensor makes it possible to detect from 0.1 to 100 nM of OTA (limit of detection: 0.02 nM in the presence of at least 50 fold excess of ochratoxin B. The applicability of the aptasensor for real sample assay was confirmed by testing spiked beer samples. The recovery of 2 nM OTA was found to be 70% for light beer and 78% for dark beer.

  15. Modeling of Polymer Erosion

    OpenAIRE

    Göpferich, Achim; Langer, Robert S.

    1993-01-01

    The erosion of bioerodible polymers depends on many factors including the polymer chain length, bond cleavage velocity, swellability, crystallinity, and water diffusivity in the polymer matrix. This multitude of parameters makes modeling of erosion difficult. Only a few models exist that describe morphological changes of polymers during erosion qualitatively. In the present approach the polymer matrix was represented as the sum of small individual polymer matrix parts. The factors that determ...

  16. Biodegradable polymers derived from renewable resources: Highly branched copolymers of itaconic anhydride

    Science.gov (United States)

    Wallach, Joshua Andrew

    In an effort to design cyclic anhydride containing polymers that are derived from renewable resources and have biodegradable characteristics, three copolymer systems using itaconic anhydride have been studied. Two of the systems were copolymers with stearate based monomers; vinyl stearate and stearyl methacrylate, while the third was a copolymer with a methacrylate terminated poly (lactic acid) (PLA) macromonomer. For the stearate systems, stearyl methacrylate showed good copolymerization with equal conversions for both monomers. On the other hand vinyl stearate did not show as good results due to its decreased reactivity, which resulted in a copolymer highly enriched in itaconic anhydride with significant amounts of unreacted vinyl stearate under all copolymer compositions. These differing results were confirmed through analysis of reactivity ratios showing a results that are more favorable for copolymerization for the methacrylate system. Copolymers from both systems showed single melting transitions in a precarious range of 45--50°C arising from the stearyl side groups, though after quenching from the melt this shifted to below room temperature. Anhydride retention was confirmed through structural analysis. Similar to the stearyl methacrylate system, methacrylate terminated PLA macromonomers were copolymerized with itaconic anhydride. PLA's acceptance as a biodegradable material derived from renewable resources, make it a viable choice, with which to design anhydride containing copolymers. Good copolymerization was shown for all compositions studied with retention of the anhydride, though at high itaconic anhydride concentrations conversions were reduced significantly. Copolymers showed glass transition temperatures ranging from 32°C for 85 mole % PLA macromonomer to 73°C for 85 mole % itaconic anhydride. An effort to produce PLA macromonomers through a process of chemical recycling commercial PLA was also undertaken. Promising results were obtained showing

  17. The Considere condition and rapid stretching of linear and branched polymer melts

    DEFF Research Database (Denmark)

    McKinley, Gareth H; Hassager, Ole

    1999-01-01

    to larger Hencky strains as the number of branches is increased. Numerical computations at finite Deborah numbers also show that there is an optimal range of deformation rates over which homogeneous extensions can be maintained to large strain. We also consider other rapid homogeneous stretching...... deformations, such as biaxial and planar stretching, and show that the degree of stabilization afforded by inclusion of material with long-chain branching is a sensitive function of the imposed mode of deformation....

  18. INVERSION SYMMETRY, ARCHITECTURE AND DISPERSITY, AND THEIR EFFECTS ON THERMODYNAMICS IN BULK AND CONFINED REGIONS: FROM RANDOMLY BRANCHED POLYMERS TO LINEAR CHAINS, STARS AND DENDRIMERS

    Directory of Open Access Journals (Sweden)

    P.D.Gujrati

    2002-01-01

    Full Text Available Theoretical evidence is presented in this review that architectural aspects can play an important role, not only in the bulk but also in confined geometries by using our recursive lattice theory, which is equally applicable to fixed architectures (regularly branched polymers, stars, dendrimers, brushes, linear chains, etc. and variable architectures, i.e. randomly branched structures. Linear chains possess an inversion symmetry (IS of a magnetic system (see text, whose presence or absence determines the bulk phase diagram. Fixed architectures possess the IS and yield a standard bulk phase diagram in which there exists a theta point at which two critical lines C and C' meet and the second virial coefficient A2 vanishes. The critical line C appears only for infinitely large polymers, and an order parameter is identified for this criticality. The critical line C' exists for polymers of all sizes and represents phase separation criticality. Variable architectures, which do not possess the IS, give rise to a topologically different phase diagram with no theta point in general. In confined regions next to surfaces, it is not the IS but branching and monodispersity, which becomes important in the surface regions. We show that branching plays no important role for polydisperse systems, but become important for monodisperse systems. Stars and linear chains behave differently near a surface.

  19. Shape memory polymers

    Science.gov (United States)

    Wilson, Thomas S.; Bearinger, Jane P.

    2015-06-09

    New shape memory polymer compositions, methods for synthesizing new shape memory polymers, and apparatus comprising an actuator and a shape memory polymer wherein the shape memory polymer comprises at least a portion of the actuator. A shape memory polymer comprising a polymer composition which physically forms a network structure wherein the polymer composition has shape-memory behavior and can be formed into a permanent primary shape, re-formed into a stable secondary shape, and controllably actuated to recover the permanent primary shape. Polymers have optimal aliphatic network structures due to minimization of dangling chains by using monomers that are symmetrical and that have matching amine and hydroxyl groups providing polymers and polymer foams with clarity, tight (narrow temperature range) single transitions, and high shape recovery and recovery force that are especially useful for implanting in the human body.

  20. Polymer friction Molecular Dynamics

    OpenAIRE

    Sivebæk, Ion Marius; Samoilov, Vladimir N.; Persson, Bo N. J.

    2010-01-01

    We present molecular dynamics friction calculations for confined hydrocarbon solids with molecular lengths from 20 to 1400 carbon atoms. Two cases are considered: a) polymer sliding against a hard substrate, and b) polymer sliding on polymer. In the first setup the shear stresses are relatively independent of molecular length. For polymer sliding on polymer the friction is significantly larger, and dependent on the molecular chain length. In both cases, the shear stresses are proportional to ...

  1. Friction between Polymer Brushes

    OpenAIRE

    Sokoloff, J. B.

    2006-01-01

    By solving the equilibrium equations for a polymer in a neutral polymer brush, the degree of interpenetration of two polymer brushes in contact and near contact is calculated. These results are used to calculate values of the force of static friction in agreement with recent friction measurements for polymer brush lubricated surfaces. It is shown that at sufficiently light loads polymer brush coated surfaces can slide, with the load supported entirely by osmotic pressure, at a sufficiently la...

  2. Post polymerization cure shape memory polymers

    Science.gov (United States)

    Wilson, Thomas S; Hearon, Michael Keith; Bearinger, Jane P

    2014-11-11

    This invention relates to chemical polymer compositions, methods of synthesis, and fabrication methods for devices regarding polymers capable of displaying shape memory behavior (SMPs) and which can first be polymerized to a linear or branched polymeric structure, having thermoplastic properties, subsequently processed into a device through processes typical of polymer melts, solutions, and dispersions and then crossed linked to a shape memory thermoset polymer retaining the processed shape.

  3. Polymer nanocomposites: polymer and particle dynamics

    KAUST Repository

    Kim, Daniel

    2012-01-01

    Polymer nanocomposites containing nanoparticles smaller than the random coil size of their host polymer chains are known to exhibit unique properties, such as lower viscosity and glass transition temperature relative to the neat polymer melt. It has been hypothesized that these unusual properties result from fast diffusion of the nanostructures in the host polymer, which facilitates polymer chain relaxation by constraint release and other processes. In this study, the effects of addition of sterically stabilized inorganic nanoparticles to entangled cis-1,4-polyisoprene and polydimethylsiloxane on the overall rheology of nanocomposites are discussed. In addition, insights about the relaxation of the host polymer chains and transport properties of nanoparticles in entangled polymer nanocomposites are presented. The nanoparticles are found to act as effective plasticizers for their entangled linear hosts, and below a critical, chemistry and molecular-weight dependent particle volume fraction, lead to reduced viscosity, glass transition temperature, number of entanglements, and polymer relaxation time. We also find that the particle motions in the polymer host are hyperdiffusive and at the nanoparticle length scale, the polymer host acts like a simple, ideal fluid and the composites\\' viscosity rises with increasing particle concentration. © 2012 The Royal Society of Chemistry.

  4. Molecular rheology of branched polymers: Decoding and exploring the role of architectural dispersity through a synergy of anionic synthesis, interaction chromatography, rheometry and modeling

    KAUST Repository

    Van Ruymbeke, Evelyne

    2014-01-01

    An emerging challenge in polymer physics is the quantitative understanding of the influence of a macromolecular architecture (i.e., branching) on the rheological response of entangled complex polymers. Recent investigations of the rheology of well-defined architecturally complex polymers have determined the composition in the molecular structure and identified the role of side-products in the measured samples. The combination of different characterization techniques, experimental and/or theoretical, represents the current state-of-the-art. Here we review this interdisciplinary approach to molecular rheology of complex polymers, and show the importance of confronting these different tools for ensuring an accurate characterization of a given polymeric sample. We use statistical tools in order to relate the information available from the synthesis protocols of a sample and its experimental molar mass distribution (typically obtained from size exclusion chromatography), and hence obtain precise information about its structural composition, i.e. enhance the existing sensitivity limit. We critically discuss the use of linear rheology as a reliable quantitative characterization tool, along with the recently developed temperature gradient interaction chromatography. The latter, which has emerged as an indispensable characterization tool for branched architectures, offers unprecedented sensitivity in detecting the presence of different molecular structures in a sample. Combining these techniques is imperative in order to quantify the molecular composition of a polymer and its consequences on the macroscopic properties. We validate this approach by means of a new model asymmetric comb polymer which was synthesized anionically. It was thoroughly characterized and its rheology was carefully analyzed. The main result is that the rheological signal reveals fine molecular details, which must be taken into account to fully elucidate the viscoelastic response of entangled branched

  5. Control of the anchoring behavior of polymer-dispersed liquid crystals: effect of branching in the side chains of polyacrylates.

    Science.gov (United States)

    Zhou, Jian; Collard, David M; Park, Jung O; Srinivasarao, Mohan

    2002-08-28

    A temperature-driven anchoring transition in a polymer/nematic fluid composite that is far from the bulk nematic-isotropic transition temperature is reported. A series of poly(methylheptyl acrylates) were studied to probe the subtle effects of the side chain structure of the polymer on control of the anchoring. A polymer-dispersed liquid crystal film made from TL205 and 1-methylheptyl acrylate shows only planar anchoring over the temperature range studied, while the films made from TL205 and each of the other methylheptyl acrylates or n-heptyl acrylate show the homeotropic-to-planar anchoring transition at temperatures between 70 and 78 degrees C. An interfacial model is proposed in which the different conformation of the side chains is suggested as the cause for the dramatic difference in the observed anchoring behavior. PMID:12188649

  6. High cation transport polymer electrolyte

    Science.gov (United States)

    Gerald, II, Rex E.; Rathke, Jerome W.; Klingler, Robert J.

    2007-06-05

    A solid state ion conducting electrolyte and a battery incorporating same. The electrolyte includes a polymer matrix with an alkali metal salt dissolved therein, the salt having an anion with a long or branched chain having not less than 5 carbon or silicon atoms therein. The polymer is preferably a polyether and the salt anion is preferably an alkyl or silyl moiety of from 5 to about 150 carbon/silicon atoms.

  7. Loop polymer brushes from polymer single crystals

    Science.gov (United States)

    Zhou, Tian; Li, Christopher

    2014-03-01

    Loop polymer brushes represent a category of polymer brushes with both chain ends being tethered to a surface or interface with sufficiently high density. Due to this morphological difference, loop brushes exhibit distinct properties compared with traditional polymer brushes with single chain end being tethered. In our study, α, ω-functionalized polycaprolactone (PCL) single crystals were prepared as templates for polymer brush synthesis. By carefully controlling crystallization condition and immobilization, looped polymer brushes were successfully prepared. Comprehensive studies on the morphology and physical properties of these polymer brushes were carried out using Atomic Force Microscopy and FTIR. Advantages of using this method include exclusive loop morphology, high grafting density, controlled tethering sites and tunable loop size.

  8. Synthesis and characterization of branched polymers from lipase-catalyzed trimethylolpropane copolymerizations.

    Science.gov (United States)

    Kulshrestha, Ankur S; Gao, Wei; Fu, Hongyong; Gross, Richard A

    2007-06-01

    Lipase-catalyzed terpolymerizations were performed with the monomers trimethylolpropane (B3), 1,8-octanediol (B2), and adipic acid (A2). Polymerizations were performed in bulk, at 70 degrees C, for 42 h, using immobilized lipase B from Candida antartica (Novozyme-435) as a catalyst. To determine the substitution pattern of trimethylolpropane (TMP) in copolymers, model compounds with variable degrees of acetylation were synthesized. Inverse-gated 13C NMR spectra were recorded to first determine the chemical shift positions for mono-, di-, and trisubstituted TMP units and, subsequently, to determine substitution of TMP units along chains. Variation of TMP in the monomer feed gave copolymers with degrees of branching (DB) from 20% to 67%. In one example, a hyperbranched copolyester with 53 mol % TMP adipate units was formed in 80% yield, with Mw 14 100 (relative to polystyrene standards), Mw/Mn 5.3, and DB 36%. Thermal and crystalline properties of the copolyesters were studied by thermogravimetric analysis and differential scanning calorimetry.

  9. CLASSIFICATION OF BIODEGRADABLE POLYMERS

    Directory of Open Access Journals (Sweden)

    I. I. Karpunin

    2015-01-01

    Full Text Available The executed investigations have made it possible to ascertain that a morphological structure of starch granules mainly determine technological peculiarities of starch isolation from raw material, its modification and its later use. Morphological structure of starch granules primarily depends on type of plant starch-containing raw material which has been used for its isolation. Class of raw material exerts a strong impact on the shape and size of the granules. Linear “light” amylose chains and “heavy” amylopectin branch chains form a starch granule ultrastructure. X-ray research has proved that starch granules are characterized by presence of interlacing amorphous and crystalline regions. In this case polymer orientation using stretching of the obtained end product influences on its physical and mechanical  indices which are increasing due to polymer orientation. For the purpose of packaging orientation of polymer films can solve such important problems as significant improvement of operational properties, creation of  thermosetting film materials, improvement of qualitative indices of the recycled film.Results of the conducted research have proved the fact that it is necessary to make changes in technology in order to increase biological degradability of the recycled packaging made from polymers and improve physical and mechanical indices. In this regard film production technology presupposes usage of such substances as stark and others which are characterized by rather large presence of branch chains of molecules and interlacing amorphous and crystalline regions. Such approach makes it possible to obtain after-use package which is strong and quickly degradable by micro-organisms.

  10. Synthesis, Morphology, and Optical Properties of Au/CdS Hybrid Nanocomposites Stabilized by Branched Polymer Matrices

    Directory of Open Access Journals (Sweden)

    V. A. Chumachenko

    2016-01-01

    Full Text Available Metal/semiconductor (Au/CdS nanocomposites were synthesized in the solution of branched D-g-PAA polymer. TEM and DLS of Au/CdS/D-g-PAA nanocomposites revealed complicated nanocomposite structure consisting of the Au nanoparticles (NPs of 6 nm in size surrounded by small CdS NPs with size of 3 nm. These nanocomposites formed the aggregates-clusters with average size of 50–800 nm. Absorption spectra of Au/CdS nanocomposites consist of the bands of excitons in CdS NPs and surface plasmons in Au ones. The surface plasmon band of gold NPs is red shifted and broadened in Au/CdS/D-g-PAA nanocomposites comparing to the one of Au NPs in Au/D-g-PAA proving the fact of close location of CdS and Au NPs in the synthesized Au/CdS/D-g-PAA nanocomposites. The PL spectra of Au/CdS nanocomposites originate from the radiative transitions in excitons in CdS NPs. The 4-fold increase of intensity of free exciton PL is observed for CdS NPs in Au/CdS/D-g-PAA comparing to CdS ones in CdS/D-g-PAA that is due to PL enhancement by local field of surface plasmons of Au NPs. Also, the 12-fold decrease of intensity of localized exciton PL is observed for CdS NPs in Au/CdS/D-g-PAA comparing to CdS ones in CdS/D-g-PAA. Most probably, it is due to passivation of the surface of CdS NPs carried out by the Au ones.

  11. Cross-linked branching nanohybrid polymer electrolyte with monodispersed TiO2 nanoparticles for high performance lithium-ion batteries

    Science.gov (United States)

    Ma, Cheng; Zhang, Jinfang; Xu, Mingquan; Xia, Qingbing; Liu, Jiatu; Zhao, Shuai; Chen, Libao; Pan, Anqiang; Ivey, Douglas G.; Wei, Weifeng

    2016-06-01

    Nanohybrid polymer electrolytes (NHPE) with ceramic particles have attracted significant attention owing to their improvement in electrochemical performance. However, particle aggregation and weak nanoparticle/polymer matrix interaction restrict their further application in lithium-ion batteries (LIBs). We demonstrate a facile in-situ polymerization/crystallization method to synthesize a homogeneous TiO2-grafted NHPE with a cross-linked branching structure, comprised of ion-conducting poly(ethylene glycol) methyl ether methacrylate (PEGMEM) and non-polar stearyl methacrylate (SMA). This technique is different from existing methods of blending functionalized ceramic particles into the polymer matrix. Highly monodispersed TiO2 nanocrystals enhance the effective interfacial interactions between particles and polymer matrix, which suppress the crystallization of ethylene oxide (EO) groups and facilitate forming continuously interconnected ion-conducting channels. Moreover, an increased dissociation degree of Li salt can also be achieved. The TiO2-grafted NHPE exhibits superior electrochemical properties with an ionic conductivity of 1.1 × 10-4 S cm-1 at 30 °C, a high lithium ion transference number and excellent interfacial compatibility with the lithium electrode. In particular, a lithium-ion battery based on TiO2-grafted NHPE demonstrates good C-rate performance, as well as excellent cycling stability with an initial discharge capacity of 153.5 mAh g-1 and a capacity retention of 96% after 300 cycles at 1 C (80 °C).

  12. Polymer Fluid Dynamics.

    Science.gov (United States)

    Bird, R. Byron

    1980-01-01

    Problems in polymer fluid dynamics are described, including development of constitutive equations, rheometry, kinetic theory, flow visualization, heat transfer studies, flows with phase change, two-phase flow, polymer unit operations, and drag reduction. (JN)

  13. Polymer composites containing nanotubes

    Science.gov (United States)

    Bley, Richard A. (Inventor)

    2008-01-01

    The present invention relates to polymer composite materials containing carbon nanotubes, particularly to those containing singled-walled nanotubes. The invention provides a polymer composite comprising one or more base polymers, one or more functionalized m-phenylenevinylene-2,5-disubstituted-p-phenylenevinylene polymers and carbon nanotubes. The invention also relates to functionalized m-phenylenevinylene-2,5-disubstituted-p-phenylenevinylene polymers, particularly to m-phenylenevinylene-2,5-disubstituted-p-phenylenevinylene polymers having side chain functionalization, and more particularly to m-phenylenevinylene-2,5-disubstituted-p-phenylenevinylene polymers having olefin side chains and alkyl epoxy side chains. The invention further relates to methods of making polymer composites comprising carbon nanotubes.

  14. Low half-wave voltage Y-branch electro-optic polymer modulator based on side-chain polyurethane-imide

    Science.gov (United States)

    Tang, Jie; Wang, Long-De; Li, Ruo-Zhou; Zhang, Qiang; Zhang, Tong

    2016-06-01

    A Y-branch electro-optic (EO) polymer modulator has been designed and fabricated. High performance side-chain polyurethane-imide (PUI) with a high EO coefficient of larger than 50 pm/V and a moderate glass-transition temperature (Tg) of 206∘C is used as EO polymer core layer of the modulator. The fabricated phase modulator exhibits a low half-wave voltage of 1.94 V at 1550 nm in single arm modulation with 1 cm EO interaction length and 2 cm total length. The results show that the modulator fabricated by side-chain PUI EO materials possesses potential applications in low driving voltage and low cost optical systems.

  15. Topological Polymer Chemistry for Designing New Macromolecular Architectures

    Institute of Scientific and Technical Information of China (English)

    Y. Tezuka

    2005-01-01

    @@ 1Introduction The precise control in polymer architectures has been an ongoing challenge in synthetic polymer chemistry, since new polymer topologies will realize unprecedented properties and functions in polymeric materials.In particular, topologically unique macromolecules comprising single cyclic and multicyclic polymer units have gained growing interests due to their distinctive behaviors from linear and branched counterparts[1-4]. See Fig. 1.

  16. Fire-safe polymers and polymer composites

    Science.gov (United States)

    Zhang, Huiqing

    The intrinsic relationships between polymer structure, composition and fire behavior have been explored to develop new fire-safe polymeric materials. Different experimental techniques, especially three milligram-scale methods---pyrolysis-combustion flow calorimetry (PCFC), simultaneous thermal analysis (STA) and pyrolysis GC/MS---have been combined to fully characterize the thermal decomposition and flammability of polymers and polymer composites. Thermal stability, mass loss rate, char yield and properties of decomposition volatiles were found to be the most important parameters in determining polymer flammability. Most polymers decompose by either an unzipping or a random chain scission mechanism with an endothermic decomposition of 100--900 J/g. Aromatic or heteroaromatic rings, conjugated double or triple bonds and heteroatoms such as halogens, N, O, S, P and Si are the basic structural units for fire-resistant polymers. The flammability of polymers can also be successfully estimated by combining pyrolysis GC/MS results or chemical structures with TGA results. The thermal decomposition and flammability of two groups of inherently fire-resistant polymers---poly(hydroxyamide) (PHA) and its derivatives, and bisphenol C (BPC II) polyarylates---have been systematically studied. PHA and most of its derivatives have extremely low heat release rates and very high char yields upon combustion. PHA and its halogen derivatives can completely cyclize into quasi-polybenzoxazole (PBO) structures at low temperatures. However, the methoxy and phosphate derivatives show a very different behavior during decomposition and combustion. Molecular modeling shows that the formation of an enol intermediate is the rate-determining step in the thermal cyclization of PHA. BPC II-polyarylate is another extremely flame-resistant polymer. It can be used as an efficient flame-retardant agent in copolymers and blends. From PCFC results, the total heat of combustion of these copolymers or blends

  17. Comparison of the Photovoltaic Characteristics and Nanostructure of Fullerenes Blended with Conjugated Polymers with Siloxane-Terminated and Branched Aliphatic Side Chains

    KAUST Repository

    Kim, Do Hwan

    2013-02-12

    All-organic bulk heterojunction solar cells based on blends of conjugated polymers with fullerenes have recently surpassed the 8% efficiency mark and are well on their way to the industrially relevant ∼15% threshold. Using a low band-gap conjugated polymer, we have recently shown that polymer side chain engineering can lead to dramatic improvement in the in-plane charge carrier mobility. In this article, we investigate the effectiveness of siloxy side chain derivatization in controlling the photovoltaic performance of polymer:[6,6]-phenyl-C[71]-butyric acid methyl ester (PC71BM) blends and hence its influence on charge transport in the out-of-plane direction relevant for organic solar cells. We find that, in neat blends, the photocurrent of the polymer with siloxy side chains (PII2T-Si) is 4 times greater than that in blends using the polymer with branched aliphatic side chains (PII2T-ref). This difference is due to a larger out-of-plane hole mobility for PII2T-Si brought about by a largely face-on crystallite orientation as well as more optimal nanoscale polymer:PC71BM mixing. However, upon incorporating a common processing additive, 1,8-diiodooctane (DIO), into the spin-casting blend solution and following optimization, the PII2T-ref:PC71BM OPV device performance undergoes a large improvement and becomes the better-performing device, almost independent of DIO concentration (>1%). We find that the precise amount of DIO plays a larger role in determining the efficiency of PII2T-Si:PC71BM, and even at its maximum, the device performance lags behind optimized PII2T-ref:PC71BM blends. Using a combination of atomic force microscopy and small- and wide-angle X-ray scattering, we are able to elucidate the morphological modifications associated with the DIO-induced changes in both the nanoscale morphology and the molecular packing in blend films. © 2012 American Chemical Society.

  18. Nanoporous polymer electrolyte

    Science.gov (United States)

    Elliott, Brian; Nguyen, Vinh

    2012-04-24

    A nanoporous polymer electrolyte and methods for making the polymer electrolyte are disclosed. The polymer electrolyte comprises a crosslinked self-assembly of a polymerizable salt surfactant, wherein the crosslinked self-assembly includes nanopores and wherein the crosslinked self-assembly has a conductivity of at least 1.0.times.10.sup.-6 S/cm at 25.degree. C. The method of making a polymer electrolyte comprises providing a polymerizable salt surfactant. The method further comprises crosslinking the polymerizable salt surfactant to form a nanoporous polymer electrolyte.

  19. Polymer friction Molecular Dynamics

    DEFF Research Database (Denmark)

    Sivebæk, Ion Marius; Samoilov, Vladimir N.; Persson, Bo N. J.

    We present molecular dynamics friction calculations for confined hydrocarbon solids with molecular lengths from 20 to 1400 carbon atoms. Two cases are considered: a) polymer sliding against a hard substrate, and b) polymer sliding on polymer. In the first setup the shear stresses are relatively...... independent of molecular length. For polymer sliding on polymer the friction is significantly larger, and dependent on the molecular chain length. In both cases, the shear stresses are proportional to the squeezing pressure and finite at zero load, indicating an adhesional contribution to the friction force....

  20. Polymer dynamics from synthetic polymers to proteins

    Indian Academy of Sciences (India)

    D Richter; R Biehl; M Monkenbush; B Hoffmann; R Merkel

    2008-10-01

    Starting from the standard model of polymer motion - the Rouse model - we briefly present some key experimental results on the mesoscopic dynamics of polymer systems. We touch the role of topological confinement as expressed in the reptation model and discuss in some more detail processes limiting the confinement. In the second part we relate to some new developments concerning the measurement of large-scale internal dynamics of proteins by neutron spin echo.

  1. CO2 -Responsive polymers.

    Science.gov (United States)

    Lin, Shaojian; Theato, Patrick

    2013-07-25

    This Review focuses on the recent progress in the area of CO2 -responsive polymers and provides detailed descriptions of these existing examples. CO2 -responsive polymers can be categorized into three types based on their CO2 -responsive groups: amidine, amine, and carboxyl groups. Compared with traditional temperature, pH, or light stimuli-responsive polymers, CO2 -responsive polymers provide the advantage to use CO2 as a "green" trigger as well as to capture CO2 directly from air. In addition, the current challenges of CO2 -responsive polymers are discussed and the different solution methods are compared. Noteworthy, CO2 -responsive polymers are considered to have a prosperous future in various scientific areas.

  2. Polymer radiation chemistry

    International Nuclear Information System (INIS)

    This article reviews some of the work carried out in the Polymer and Radiation Group at the University of Queensland over the past ten years. The objective of the work has been to investigate the relationships between polymer structure and sensitivity towards high energy radiation, including 60Co gamma radiation, electron beams and UV radiation. A range of synthetic polymers containing carboxyl groups, acrylate groups, sulfone groups, amide linkages and aromatic residues have been investigated. (author). 18 refs, 2 figs, 4 tabs

  3. BSA Hybrid Synthesized Polymer

    Institute of Scientific and Technical Information of China (English)

    Zong Bin LIU; Xiao Pei DENG; Chang Sheng ZHAO

    2006-01-01

    Bovine serum albumin (BSA), a naturally occurring biopolymer, was regarded as a polymeric material to graft to an acrylic acid (AA)-N-vinyl pyrrolidone (NVP) copolymer to form a biomacromolecular hybrid polymer. The hybrid polymer can be blended with polyethersulfone (PES) to increase the hydrophilicity of the PES membrane, which suggested that the hybrid polymer might have a wide application in the modification of biomaterials.

  4. Multilayer polymer microspot targets

    International Nuclear Information System (INIS)

    Last year the authors reported on the development of a seeded microspot x-ray diagnostic target. This target consisted of a 300-μm-diam, 2-μm-thick disk of silicon or sulfur-seeded hydrocarbon polymer nested tightly in a hole in a 2-μm-thick film of pure hydrocarbon polymer. This year they extended our work on the microspot target, fully encapsulating the microspot in what they call the multilayer polymer microspot target

  5. Nanostructured polymers for photonics

    OpenAIRE

    Chantal Paquet; Eugenia Kumacheva

    2008-01-01

    We review recent progress in the development of polymer nanostructured materials with periodic structures and compositions having applications in photonics and optical data storage. This review provides a brief description of the microfabrication and self-assembly methods used for the production of polymer materials with periodic structures, and highlights the properties and applications of photonic materials derived from block copolymers, colloid crystals, and microfabricated polymers. We co...

  6. All Polymer Micropump

    OpenAIRE

    Hansen, Thomas Steen; Larsen, Niels Bent; Hassager, Ole

    2008-01-01

    In this thesis an all polymer micropump, and the fabrication method required to fabricate this, are examined. Polymer microfluidic. devices are of major scientific interest because they can combine complicated chemical and biological analys~s in cheap and disposable devices. The electrode system in the micropump is based on the conducting polymer poly(3,4 ethylenedioxythiophene) (PEDOT). The majority of the work conducted was therefore aimed at developing methods for patterning and processing...

  7. Thermally conductive polymers

    Science.gov (United States)

    Byrd, N. R.; Jenkins, R. K.; Lister, J. L. (Inventor)

    1971-01-01

    A thermally conductive polymer is provided having physical and chemical properties suited to use as a medium for potting electrical components. The polymer is prepared from hydroquinone, phenol, and formaldehyde, by conventional procedures employed for the preparation of phenol-formaldehyde resins. While the proportions of the monomers can be varied, a preferred polymer is formed from the monomers in a 1:1:2.4 molar or ratio of hydroquinone:phenol:formaldehyde.

  8. Antioxidant Stabilisation of Polymers

    Science.gov (United States)

    Shlyapnikov, Yurii A.

    1981-06-01

    Physicochemical aspects of the stabilisation of polymers are discussed. Attention is paid mainly to the aging and stabilisation of polymers under processing conditions. Topics considered are the kinetics and mechanism of the high-temperature oxidation of polymers, critical phenomena in the inhibited oxidation of polymers, the theory of synergism and antagonism among antioxidants, the reasons for differences in efficiency of antioxidants, and certain aspects of the relation between the efficiency of antioxidants and their molecular structure. A list of 132 references is included.

  9. Characterisation of polymers, 1

    CERN Document Server

    Crompton, Roy

    2008-01-01

    This essential guide to Polymer Characterisation is a complete compendium of methodologies that have evolved for the determination of the chemical composition of polymers. This 478-page book gives an up-to-date and thorough exposition of the state-of-the-art theories and availability of instrumentation needed to effect chemical and physical analysis of polymers. This is supported by approximately 1200 references. Volume 1 covers the methodology used for the determination of metals, non-metals and organic functional groups in polymers, and for the determination of the ratio in which different m

  10. Biopolymers Versus Synthetic Polymers

    Directory of Open Access Journals (Sweden)

    Florentina Adriana Cziple

    2008-10-01

    Full Text Available This paper present an overview of important synthetic and natural polymers with emphasis on polymer structure, the chemistry of polymer formation. an introduction to polymer characterization. The biodegradation process can take place aerobically and anaerobically with or without the presence of light. These factors allow for biodegradation even in landfill conditions which are normally inconducive to any degradation. The sheeting used to make these packages differs significantly from other “degradable plastics” in the market as it does not attempt to replace the current popular materials but instead enhances them by rendering them biodegradable.

  11. Nanostructured polymers for photonics

    Directory of Open Access Journals (Sweden)

    Chantal Paquet

    2008-04-01

    Full Text Available We review recent progress in the development of polymer nanostructured materials with periodic structures and compositions having applications in photonics and optical data storage. This review provides a brief description of the microfabrication and self-assembly methods used for the production of polymer materials with periodic structures, and highlights the properties and applications of photonic materials derived from block copolymers, colloid crystals, and microfabricated polymers. We conclude with a summary of current and future research efforts and opportunities in the development of polymer materials for photonic applications.

  12. Triclosan antimicrobial polymers

    Science.gov (United States)

    Petersen, Richard C.

    2016-01-01

    Triclosan antimicrobial molecular fluctuating energies of nonbonding electron pairs for the oxygen atom by ether bond rotations are reviewed with conformational computational chemistry analyses. Subsequent understanding of triclosan alternating ether bond rotations is able to help explain several material properties in Polymer Science. Unique bond rotation entanglements between triclosan and the polymer chains increase both the mechanical properties of polymer toughness and strength that are enhanced even better through secondary bonding relationships. Further, polymer blend compatibilization is considered due to similar molecular relationships and polarities. With compatibilization of triclosan in polymers a more uniform stability for nonpolar triclosan in the polymer solid state is retained by the antimicrobial for extremely low release with minimum solubility into aqueous solution. As a result, triclosan is projected for long extended lifetimes as an antimicrobial polymer additive. Further, triclosan rapid alternating ether bond rotations disrupt secondary bonding between chain monomers in the resin state to reduce viscosity and enhance polymer blending. Thus, triclosan is considered for a polymer additive with multiple properties to be an antimicrobial with additional benefits as a nonpolar toughening agent and a hydrophobic wetting agent. The triclosan material relationships with alternating ether bond rotations are described through a complete different form of medium by comparisons with known antimicrobial properties that upset bacterial cell membranes through rapid fluctuating mechanomolecular energies. Also, triclosan bond entanglements with secondary bonding can produce structural defects in weak bacterial lipid membranes requiring pliability that can then interfere with cell division. Regarding applications with polymers, triclosan can be incorporated by mixing into a resin system before cure, melt mixed with thermoplastic polymers that set on cooling

  13. Approaches for Making High Performance Polymer Materials from Commodity Polymers

    Institute of Scientific and Technical Information of China (English)

    Xu Xi

    2004-01-01

    A brief surrey of ongoing research work done for improving and enhancing the properties of commodity polymers by the author and author's colleagues is given in this paper. A series of high performance polymers and polymer nanomaterials were successfully prepared through irradiation and stress-induced reactions of polymers and hydrogen bonding. The methods proposed are viable, easy in operation, clean and efficient.1. The effect of irradiation source (UV light, electron beam, γ -ray and microwave), irradiation dose, irradiation time and atmosphere etc. on molecular structure of polyolefine during irradiation was studied. The basic rules of dominating oxidation, degradation and cross-linking reactions were mastered. Under the controlled conditions, cross-linking reactions are prevented, some oxygen containing groups are introduced on the molecular chain of polyolefine to facilitate the interface compatibility of their blends. A series of high performance polymer materials: u-HDPE/PA6,u-HDPE/CaCO3, u-iPP/STC, γ-HDPE/STC, γ-LLDPE/ATH, e-HDPE, e-LLDPE and m-HDPEfilled system were prepared (u- ultraviolet light irradiated, γ- γ-ray irradiated, e- electron beam irradiated, m- microwave irradiated)2. The effect of ultrasonic irradiation, jet and pan-milling on structure and changes in properties of polymers were studied. Imposition of critical stress on polymer chain can cause the scission of bonds to form macroradicals. The macroradicals formed in this way may recombine or react with monomer or other radicals to form linear, branched or cross-linked polymers or copolymers. About 20 kinds of block/graft copolymers have been synthesized from polymer-polymer or polymer-monomer through ultrasonic irradiation.Through jet-milling, the molecular weight of PVC is decreased somewhat, the intensity of its crystalline absorption bonds becomes indistinct. The processability, the yield strength, strength at break and elongation at break of PVC get increased quite a lot after

  14. Polymers in Waveguide Packaging

    Institute of Scientific and Technical Information of China (English)

    G; Z.; Xiao; C.; P.; Grover

    2003-01-01

    Polymers were successfully used in the packaging of waveguide-based photonic components in the area of fiber-to-waveguide coupling, waveguide die attachment, strain relief, and waveguide encapsulation. The application results of these polymers were described in this paper.

  15. Stiff Quantum Polymers

    OpenAIRE

    Kleinert, H

    2007-01-01

    At ultralow temperatures, polymers exhibit quantum behavior, which is calculated here for the second and fourth moments of the end-to-end distribution in the large-stiffness regime. The result should be measurable for polymers in wide optical traps.

  16. Doped Chiral Polymer Metamaterials Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Doped Chiral Polymer Metamaterials (DCPM) with tunable resonance frequencies have been developed by adding plasmonic inclusions into chiral polymers with variable...

  17. Theory of polymer blends

    International Nuclear Information System (INIS)

    We have recently developed a new theoretical approach to the study of polymer liquids. The theory is based on the ''reference interaction site model'' (RISM theory) of Chandler and Andersen, which has been successful in describing the structure of small molecule liquids. We have recently extended our polymer RISM theory to the case of polymer blends. In the present investigation we have applied this theory to two special binary blends: (1) the athermal mixture where we isolate structural effects, and (2) the isotopic mixture in which structurally identical polymer chains interact with dissimilar attractive interactions. By studying these two special cases we are able to obtain insights into the molecular factors which control the miscibility in polymer mixtures. 18 refs., 2 figs

  18. Electroactive polymers for sensing.

    Science.gov (United States)

    Wang, Tiesheng; Farajollahi, Meisam; Choi, Yeon Sik; Lin, I-Ting; Marshall, Jean E; Thompson, Noel M; Kar-Narayan, Sohini; Madden, John D W; Smoukov, Stoyan K

    2016-08-01

    Electromechanical coupling in electroactive polymers (EAPs) has been widely applied for actuation and is also being increasingly investigated for sensing chemical and mechanical stimuli. EAPs are a unique class of materials, with low-moduli high-strain capabilities and the ability to conform to surfaces of different shapes. These features make them attractive for applications such as wearable sensors and interfacing with soft tissues. Here, we review the major types of EAPs and their sensing mechanisms. These are divided into two classes depending on the main type of charge carrier: ionic EAPs (such as conducting polymers and ionic polymer-metal composites) and electronic EAPs (such as dielectric elastomers, liquid-crystal polymers and piezoelectric polymers). This review is intended to serve as an introduction to the mechanisms of these materials and as a first step in material selection for both researchers and designers of flexible/bendable devices, biocompatible sensors or even robotic tactile sensing units. PMID:27499846

  19. Semiconducting polymer LEDs

    Directory of Open Access Journals (Sweden)

    David Braun

    2002-06-01

    The field of semiconducting polymers has its root in the 1977 discovery of the semiconducting properties of polyacetylene1. This breakthrough earned Alan Heeger, Alan MacDiarmid, and Hideki Shirakawa the 2000 Nobel Prize in Chemistry for ‘the discovery and development of conductive polymers’2–5. Other review articles capture how more than two decades of developments in the physical and chemical understanding of these novel materials has led to new device applications as active and passive electronic and optoelectronic devices ranging from diodes and transistors to polymer LEDs, photodiodes, lasers, and solar cells6–11. Much interest in plastic devices derives from the opportunities to use clever control of polymer structure combined with relatively economical polymer synthesis and processing techniques to obtain simultaneous control over electronic, optical, chemical, and mechanical features5. This article focuses on the advances leading to polymer LEDs12–14.

  20. Ion Implantation of Polymers

    DEFF Research Database (Denmark)

    Popok, Vladimir

    2012-01-01

    The current paper presents a state-of-the-art review in the field of ion implantation of polymers. Numerous published studies of polymers modified by ion beams are analysed. General aspects of ion stopping, latent track formation and changes of structure and composition of organic materials...... are discussed. Related to that, the effects of radiothermolysis, degassing and carbonisation are considered. Specificity of depth distributions of implanted into polymers impurities is analysed and the case of high-fluence implantation is emphasised. Within rather broad topic of ion bombardment, the focus...... is put on the low-energy implantation of metal ions causing the nucleation and growth of nanoparticles in the shallow polymer layers. Electrical, optical and magnetic properties of metal/polymer composites are under the discussion and the approaches towards practical applications are overviewed....

  1. Antiviral Polymer Therapeutics

    DEFF Research Database (Denmark)

    Smith, Anton Allen Abbotsford

    2014-01-01

    and the drug which increased the potency of the conjugates significantly. A different approach to drug delivery is that of surface mediated drug delivery. Hydrogels of poly(vinyl alcohol) has shown great promise in this regard. The chemical opportunities of this polymer are explored through the virtues...... of reversible-addition-fragmentation chain transfer polymerization, which not only controls the size of polymer, but also allows the introduction of a terminal amine on the polymer which can be used for further conjugation. This has allowed for not only fluorescent labeling of the polymer, but also protein......The field of drug delivery is in essence an exercise in engineered pharmacokinetics. Methods of doing so have been developed through the introduction of a vehicle carrying the drug, either by encapsulation or covalent attachment. The emergence of polymer therapeutics in anticancer therapy has...

  2. Polymer wear evaluation

    DEFF Research Database (Denmark)

    Lagerbon, Mikkel; Sivebæk, Ion Marius

    2012-01-01

    Polymer wear plays an increasing role in manufacturing of machine parts for e.g. medical devices. Some of these have an expected lifetime of five to eight years during which very little wear of the components is acceptable. Too much wear compromises the dosage accuracy of the device and thereby...... the safety of the patients. Prediction of the wear of polymers is complicated by the low thermal conductivity of this kind of material. It implies that any acceleration of testing conditions by increased contact pressure and/or sliding velocity will make the polymer fail due to exaggerated heat buildup....... This is not the kind of wear observed in medical devices. In the present work a method was developed capable of evaluating the wear progression in polymer-polymer contacts. The configuration of the setup is injection moulded specimens consisting of an upper part having a toroid shape and a lower flat part. The sliding...

  3. Polymer-Polymer Miscibility and Enthalpy Relaxations

    NARCIS (Netherlands)

    Bosma, Martin; Brinke, Gerrit ten; Ellis, Thomas S.

    1988-01-01

    Annealing of polymers below the glass transition temperature results in a decrease in enthalpy that is recovered during heating. The enthalpy recovery is visible as an endothermic peak in a differential scanning calorimetry (DSC) scan. The position of this peak depends on the thermal treatment given

  4. Self reinforced polymer-polymer composites

    Directory of Open Access Journals (Sweden)

    M. Bilewicz

    2007-10-01

    Full Text Available Purpose: Purpose of this paper is the applying of new technology in injection moulding technique and investigation of reinforcement of PC as dispersed phase inside PP matrix (Table 1. Second aim of work is enrichment of those composites by nanoclay and analyzing mechanical behaviour of nanocomposites.Design/methodology/approach: According to design of experiments (DOE specimens were injection moulded in the shape of rectangular bars. Additionally advanced technology of melt manipulation inside mold cavity after injection was used. To achieve this purpose Ferromatik Milacron injection moulding machine, equipped with externally controlled mold was used.Findings: Addition of nanoclay clearly presents highly reinforced system, especially for neat matrix. Evenly dispersed PC particles within PP majority show reinforcement as well. Inducement of shear rate in injection moulding radically improved absorption of energy in nanocomposite.Research limitations/implications: Different variation of material composition, such combination with other polymers and use of different reinforcements (flexible or either rigid is required to be checked in the further work.Practical implications: Reinforcement obtained thanks to dispersed phase and nanofillers creates composites with improved mechanical properties.Originality/value: Morphology development reflects on mechanical behaviour. Its manipulation may affect and improve mechanical properties. Use of advanced technologies opens wide range of possibilities in processing of polymer based systems. At present there is limited number of research of processing-structure-properties relationships of polymer-polymer composites and nanocomposites.

  5. Mechanisms of the self-organization of star-shaped polymers with a varied structure of branching center based on fullerene C60 in solutions

    International Nuclear Information System (INIS)

    The self-organization of star-shaped polymers in toluene has been studied by small-angle neutron scattering. Polystyrene stars with a mono-C60 branching center are ordered into globular clusters (∼1700 nm in diameter), whereas stars with a double (C60-C60) center are ordered into anisotropic structures (superchains), which are linked (depending on the concentration) into triads (chain clusters ∼2500 nm in diameter). On the contrary, heteroarm polystyrene and poly-2-vinylpyridine stars with a C60 center are weakly associated into dimers. Moderately polar stars with arms composed of polystyrene and diblock copolymer (poly-2-vinylpyridine-poly-tret-butyl methacrylate) form short chains composed of four macromolecules, while stars of higher polarity based on polystyrene and poly-tret-butyl methacrylate form clusters containing ∼12 macromolecules ∼50 nm in diameter. Thus, by varying the structure of the center and the arm polarity, one can control the modes of star structuring.

  6. Neutron studies of polymers

    International Nuclear Information System (INIS)

    The possibility to contrast given fractions of a polymer system at a cost of a low enthalpy difference is responsible for the success of the neutron method. This approach is especially useful for polymers as compared to colloids or simple liquids, because of the significative intra- and inter-molecular correlations. In this respect, the pseudo diblock copolymer constitutes one of the best test molecule of homogeneous polymer system. A review is given of main results: polymer size in melts, true backbone conformation and universal constants related to polymer structures. Effects of mechanical stress, of mesogenic order have been revealed. Neutron spin-echo experiments have given characteristic dispersion relations of intra- and inter-polymer diffusive motions. The labelling method is however more powerful than first realized. The amplitude associated with a polymer structure at an interface has been obtained directly (as in ellipsometry) with the use of contrast variation. Such structures are currently investigated by neutron reflectivity. Latest developments are found in the use of spin polarized targets, from which important cross correlations are derived

  7. Polymer Science Pilot Program

    Science.gov (United States)

    Maier, Mary L.

    1996-07-01

    Natural polymers such as cellulose, proteins, and DNA have been part of earth's store of chemicals long before chemists existed. However, polymers synthesized by chemists first appeared on this planet only sixty years ago. A veritable explosion of materials first known as plastics, later polymers, followed. Today polymers, natural and synthetic, are everywhere, and it is appropriate to include an introduction to polymers in the education of future scientists. The Polymer Science Pilot Program consists of a sequence of experiences with polymers, designed to focus upon the ways in which these materials resemble and/or compare with nonpolymers in physical properties, versatility, and function. The modular format makes it possible for educators to select specific sections of the program for integration into other college chemistry courses. The team learning aspect of he program can also be recommended to educators who select a specific module. When this program was presented at a Middle Atlantic Regional Meeting of the American Chemical Society, some attendees were concerned about the limited number of participants as compared with the seemingly large number of college instructors. It was explained that the concentrated format of the four day program necessitates this instructor-to-student ratio; one class consisting of eighteen participants was tried and it was found that some aspects of the program, especially the research paper preparation, were not as thoroughly moderated.

  8. Ion implantation in polymers

    Science.gov (United States)

    Wintersgill, M. C.

    1984-02-01

    An introductory overview will be given of the effects of ion implantation on polymers, and certain areas will be examined in more detail. Radiation effects in general and ion implantation in particular, in the field of polymers, present a number of contrasts with those in ionic crystals, the most obvious difference being that the chemical effects of both the implanted species and the energy transfer to the host may profoundly change the nature of the target material. Common effects include crosslinking and scission of polymer chains, gas evolution, double bond formation and the formation of additional free radicals. Research has spanned the chemical processes involved, including polymerization reactions achievable only with the use of radiation, to applied research dealing both with the effects of radiation on polymers already in commercial use and the tailoring of new materials to specific applications. Polymers are commonly divided into two groups, in describing their behavior under irradiation. Group I includes materials which form crosslinks between molecules, whereas Group II materials tend to degrade. In basic research, interest has centered on Group I materials and of these polyethylene has been studied most intensively. Applied materials research has investigated a variety of polymers, particularly those used in cable insulation, and those utilized in ion beam lithography of etch masks. Currently there is also great interest in enhancing the conducting properties of polymers, and these uses would tend to involve the doping capabilities of ion implantation, rather than the energy deposition.

  9. Influence of Polymer Molecular Weight on Drug-Polymer Solubility

    DEFF Research Database (Denmark)

    Knopp, Matthias Manne; Olesen, Niels Erik; Holm, Per;

    2015-01-01

    In this study, the influence of polymer molecular weight on drug-polymer solubility was investigated using binary systems containing indomethacin (IMC) and polyvinylpyrrolidone (PVP) of different molecular weights. The experimental solubility in PVP, measured using a differential scanning...... the solubility in the polymer. Hence, if a drug is soluble in an analogue of the polymer, it is most likely also soluble in the polymer. In conclusion, the solubility of a given drug-polymer system is determined by the strength of the drug-polymer interactions rather than the molecular weight of the...... polymer. Therefore, during the first screenings for drug solubility in polymers, only one representative molecular weight per polymer is needed....

  10. Soluble porphyrin polymers

    Science.gov (United States)

    Gust, Jr., John Devens; Liddell, Paul Anthony

    2015-07-07

    Porphyrin polymers of Structure 1, where n is an integer (e.g., 1, 2, 3, 4, 5, or greater) ##STR00001## are synthesized by the method shown in FIGS. 2A and 2B. The porphyrin polymers of Structure 1 are soluble in organic solvents such as 2-MeTHF and the like, and can be synthesized in bulk (i.e., in processes other than electropolymerization). These porphyrin polymers have long excited state lifetimes, making the material suitable as an organic semiconductor for organic electronic devices including transistors and memories, as well as solar cells, sensors, light-emitting devices, and other opto-electronic devices.

  11. Polymer artificial muscles

    Directory of Open Access Journals (Sweden)

    Tissaphern Mirfakhrai

    2007-04-01

    Full Text Available The various types of natural muscle are incredible material systems that enable the production of large deformations by repetitive molecular motions. Polymer artificial muscle technologies are being developed that produce similar strains and higher stresses using electrostatic forces, electrostriction, ion insertion, and molecular conformational changes. Materials used include elastomers, conducting polymers, ionically conducting polymers, and carbon nanotubes. The mechanisms, performance, and remaining challenges associated with these technologies are described. Initial applications are being developed, but further work by the materials community should help make these technologies applicable in a wide range of devices where muscle-like motion is desirable.

  12. Development of Silicate Polymers

    DEFF Research Database (Denmark)

    Søgaard, Erik Gydesen; Simonsen, Morten Enggrob

      The development of inorganic polymers is a new promising technology that may be used in many applications. The syntheses of inorganic polymers are normally carried out either by mixing an amorphous material for example silicium dioxide with a mineral base or dissolving metal oxids or metal...... hydroxide in acid and increase pH to saturation of the metal hydroxide. It is assumed that the syntheses of the inorganic polymer are carried out through polymerisation of oligomers (dimer, trimer) which provide the actual unit structures of the three dimensional macromolecular structure. In this work...

  13. Lectures on random polymers

    CERN Document Server

    Caravenna, Francesco; Pétrélis, Nicolas

    2011-01-01

    These lecture notes are a guided tour through the fascinating world of polymer chains interacting with themselves and/or with their environment. The focus is on the mathematical description of a number of physical and chemical phenomena, with particular emphasis on phase transitions and space-time scaling. The topics covered, though only a selection, are typical for the area. Sections 1-3 describe models of polymers without disorder, Sections 4-6 models of polymers with disorder. Appendices A-E contain tutorials in which a number of key techniques are explained in more detail.

  14. Biomedical applications of polymers

    CERN Document Server

    Gebelein, C G

    1991-01-01

    The biomedical applications of polymers span an extremely wide spectrum of uses, including artificial organs, skin and soft tissue replacements, orthopaedic applications, dental applications, and controlled release of medications. No single, short review can possibly cover all these items in detail, and dozens of books andhundreds of reviews exist on biomedical polymers. Only a few relatively recent examples will be cited here;additional reviews are listed under most of the major topics in this book. We will consider each of the majorclassifications of biomedical polymers to some extent, inclu

  15. Polymers for Protein Conjugation

    Directory of Open Access Journals (Sweden)

    Gianfranco Pasut

    2014-01-01

    Full Text Available Polyethylene glycol (PEG at the moment is considered the leading polymer for protein conjugation in view of its unique properties, as well as to its low toxicity in humans, qualities which have been confirmed by its extensive use in clinical practice. Other polymers that are safe, biodegradable and custom-designed have, nevertheless, also been investigated as potential candidates for protein conjugation. This review will focus on natural polymers and synthetic linear polymers that have been used for protein delivery and the results associated with their use. Genetic fusion approaches for the preparation of protein-polypeptide conjugates will be also reviewed and compared with the best known chemical conjugation ones.

  16. Electroactive polymers for sensing

    Science.gov (United States)

    2016-01-01

    Electromechanical coupling in electroactive polymers (EAPs) has been widely applied for actuation and is also being increasingly investigated for sensing chemical and mechanical stimuli. EAPs are a unique class of materials, with low-moduli high-strain capabilities and the ability to conform to surfaces of different shapes. These features make them attractive for applications such as wearable sensors and interfacing with soft tissues. Here, we review the major types of EAPs and their sensing mechanisms. These are divided into two classes depending on the main type of charge carrier: ionic EAPs (such as conducting polymers and ionic polymer–metal composites) and electronic EAPs (such as dielectric elastomers, liquid-crystal polymers and piezoelectric polymers). This review is intended to serve as an introduction to the mechanisms of these materials and as a first step in material selection for both researchers and designers of flexible/bendable devices, biocompatible sensors or even robotic tactile sensing units. PMID:27499846

  17. Shape-memory polymers

    Directory of Open Access Journals (Sweden)

    Marc Behl

    2007-04-01

    Full Text Available Shape-memory polymers are an emerging class of active polymers that have dual-shape capability. They can change their shape in a predefined way from shape A to shape B when exposed to an appropriate stimulus. While shape B is given by the initial processing step, shape A is determined by applying a process called programming. We review fundamental aspects of the molecular design of suitable polymer architectures, tailored programming and recovery processes, and the quantification of the shape-memory effect. Shape-memory research was initially founded on the thermally induced dual-shape effect. This concept has been extended to other stimuli by either indirect thermal actuation or direct actuation by addressing stimuli-sensitive groups on the molecular level. Finally, polymers are introduced that can be multifunctional. Besides their dual-shape capability, these active materials are biofunctional or biodegradable. Potential applications for such materials as active medical devices are highlighted.

  18. THERMOCHROMIC POLYMER MATERIALS

    Institute of Scientific and Technical Information of China (English)

    A.Seeboth; A.Klukowska; R.Ruhmann; D.L(o)tzsch

    2007-01-01

    Thermochromic polymers will play an extremely important role in the next future.The physical background of thermochromism and the state of development of thermochromic polymers based on light absorption effects are reported.In detail.the interactions between the polymer matrix and the thermochromic composite-composed of leuco or indicator dyes-are discussed on a molecular level.Thermochromic hydrogels with extremely high transparency,an outstanding switching behavior from colorless to colored or between different colors is presented.Preparation of thermosetting and thermoplastic polymers,including the resulting optical,and,for the first time,the mechanical properties are discussed in relation to matrix tuned high-resistant microcapsules.

  19. Polymers Best Paper Award 2015

    Directory of Open Access Journals (Sweden)

    Alexander Böker

    2015-01-01

    Full Text Available Polymers is instituting an annual award to recognize the outstanding papers in the area of polymer science published in Polymers. We are pleased to announce the second “Polymers Best Paper Award” for 2015 [1]. Nominations were selected by the Editor-in-Chief and Editorial Board members of Polymers from all papers published in 2011. The awards are issued to reviews and articles respectively. We are pleased to announce that the following five papers were chosen:[...

  20. Polymers Best Paper Award 2014

    Directory of Open Access Journals (Sweden)

    Alexander Böker

    2014-01-01

    Full Text Available Polymers is instituting an annual award to recognize outstanding papers in the area of polymer science published in Polymers. We are pleased to announce the first “Polymers Best Paper Award” for 2014. Nominations were selected by the Editor-in-Chief and Editorial Board members of Polymers from all papers published in 2010. The awards are issued to reviews and articles respectively.

  1. Supramolecular polymers in inhomogeneous systems

    OpenAIRE

    Zweistra, H.J.A.

    2007-01-01

    This thesis describes theoretical results of supramolecular polymers in inhomogeneous systems. Supramolecular polymers are linear assemblies of which the monomers are joined by reversible bonds. Many types of supramolecular polymers have been synthesized in recent years. Moreover, there are numerous compounds in nature which exhibit similar behavior. Simulations of coarse-grained models of supramolecular polymers yielded new insights into the properties of supramolecular polymers in inhomogen...

  2. Edible Polymers: Challenges and Opportunities

    OpenAIRE

    Subhas C. Shit; Shah, Pathik M.

    2014-01-01

    Edible polymers have established substantial deliberation in modern eons because of their benefits comprising use as edible materials over synthetic polymers. This could contribute to the reduction of environmental contamination. Edible polymers can practically diminish the complexity and thus improve the recyclability of materials, compared to the more traditional non-environmentally friendly materials and may be able to substitute such synthetic polymers. A synthetic hydrogel polymer unlock...

  3. Polymer optical motherboard technology

    Science.gov (United States)

    Keil, N.; Yao, H.; Zawadzki, C.; Grote, N.; Schell, M.

    2008-02-01

    In this paper, different hybridly integrated optical devices including optical multiplexer/ demultiplexer and optical transceivers are described. The devices were made using polymer planar light wave circuit (P2LC) technology. Laser diodes, photodiodes, and thin-film filters have been integrated. Key issues involved in this technology, in particular the coupling between laser diodes and polymer waveguides, and between waveguides and photodiodes and also fibers are discussed.

  4. Active Polymer Gel Actuators

    OpenAIRE

    Shuji Hashimoto; Ryo Yoshida; Yusuke Hara; Shingo Maeda

    2010-01-01

    Many kinds of stimuli-responsive polymer and gels have been developed and applied to biomimetic actuators or artificial muscles. Electroactive polymers that change shape when stimulated electrically seem to be particularly promising. In all cases, however, the mechanical motion is driven by external stimuli, for example, reversing the direction of electric field. On the other hand, many living organisms can generate an autonomous motion without external driving stimuli like self-beating of he...

  5. Polymer Protected Gold Nanoparticles

    OpenAIRE

    Shan, Jun

    2006-01-01

    Polymer protected gold nanoparticles have successfully been synthesized by both "grafting-from" and "grafting-to" techniques. The synthesis methods of the gold particles were systematically studied. Two chemically different homopolymers were used to protect gold particles: thermo-responsive poly(N-isopropylacrylamide), PNIPAM, and polystyrene, PS. Both polymers were synthesized by using a controlled/living radical polymerization process, reversible addition-fragmentation chain transfer (RAFT)...

  6. Dielectric Actuation of Polymers

    OpenAIRE

    Niu, Xiaofan

    2013-01-01

    Dielectric polymers are widely used in a plurality of applications, such as electrical insulation, dielectric capacitors, and electromechanical actuators. Dielectric polymers with large strain deformations under an electric field are named dielectric elastomers (DE), because of their relative low modulus, high elongation at break, and outstanding resilience. Dielectric elastomer actuators (DEA) are superior to traditional transducers as a muscle-like technology: large strains, high energy den...

  7. Toxicology of Biomedical Polymers

    OpenAIRE

    P. V. Vedanarayanan; A. C. Fernandez

    1987-01-01

    This paper deals with the various types of polymers, used in the fabrication of medical devices, their diversity of applications and toxic hazards which may arise out of their application. The potential toxicity of monomers and the various additives used in the manufacture of biomedical polymers have been discussed along with hazards which may arise out of processing of devices such as sterilization. The importance of quality control and stringent toxicity evaluation methods have been emphasi...

  8. Rapid Polymer Sequencer

    Science.gov (United States)

    Stolc, Viktor (Inventor); Brock, Matthew W (Inventor)

    2013-01-01

    Method and system for rapid and accurate determination of each of a sequence of unknown polymer components, such as nucleic acid components. A self-assembling monolayer of a selected substance is optionally provided on an interior surface of a pipette tip, and the interior surface is immersed in a selected liquid. A selected electrical field is impressed in a longitudinal direction, or in a transverse direction, in the tip region, a polymer sequence is passed through the tip region, and a change in an electrical current signal is measured as each polymer component passes through the tip region. Each of the measured changes in electrical current signals is compared with a database of reference electrical change signals, with each reference signal corresponding to an identified polymer component, to identify the unknown polymer component with a reference polymer component. The nanopore preferably has a pore inner diameter of no more than about 40 nm and is prepared by heating and pulling a very small section of a glass tubing.

  9. Conductivity behaviour of polymer gel electrolytes: Role of polymer

    Indian Academy of Sciences (India)

    S S Sekhon

    2003-04-01

    Polymer is an important constituent of polymer gel electrolytes along with salt and solvent. The salt provides ions for conduction and the solvent helps in the dissolution of the salt and also provides the medium for ion conduction. Although the polymer added provides mechanical stability to the electrolytes yet its effect on the conductivity behaviour of gel electrolytes as well as the interaction of polymer with salt and solvent has not been conclusively established. The conductivity of lithium ion conducting polymer gel electrolytes decreases with the addition of polymer whereas in the case of proton conducting polymer gel electrolytes an increase in conductivity has been observed with polymer addition. This has been explained to be due to the role of polymer in increasing viscosity and carrier concentration in these gel electrolytes.

  10. East Coalinga polymer project: polymer comparisons. [California

    Energy Technology Data Exchange (ETDEWEB)

    Snell, G.

    1976-01-01

    Shell Oil Co. conducted a series of injection and filtration tests in the E. Colainga field, California, to determine the injection characteristics of biopolymer and polyacrylamides. The choice of Xanflood biopolymer was made in order to evaluate the relative merits of polymer flooding and waterflooding in the Temblor Zone II reservoir. Conclusions to the field injection tests were (1) Xanflood biopolymers maintain their mobility properties during these tests; (2) it is possible to remove unhydrated Xanflood biopolymer or unhydrated biopolymer and bacterial debris with DE Filtration without significant loss in biopolymer viscosity; (3) the introduction of an optimum level of shear in the biopolymer mixing process increases the mobility control available for a given concentration of polymer; (4) currently available commercial biopolymers cause well-bore impairment so that effective filtration of the polymer solution is required to maintain injectivity; (5) at test injection rates (33 bpd/ft), polyacrylamide loses most of its mobility control by shear degradation at the injection well perforations; (6) polyacrylamide can be delivered to the sand face without severe loss of viscosity; and (7) polyacrylamide will not impair the formation. (12 refs.)

  11. Precursor polymer compositions comprising polybenzimidazole

    Energy Technology Data Exchange (ETDEWEB)

    Klaehn, John R.; Peterson, Eric S.; Orme, Christopher J.

    2015-07-14

    Stable, high performance polymer compositions including polybenzimidazole (PBI) and a melamine-formaldehyde polymer, such as methylated, poly(melamine-co-formaldehyde), for forming structures such as films, fibers and bulky structures. The polymer compositions may be formed by combining polybenzimidazole with the melamine-formaldehyde polymer to form a precursor. The polybenzimidazole may be reacted and/or intertwined with the melamine-formaldehyde polymer to form the polymer composition. For example, a stable, free-standing film having a thickness of, for example, between about 5 .mu.m and about 30 .mu.m may be formed from the polymer composition. Such films may be used as gas separation membranes and may be submerged into water for extended periods without crazing and cracking. The polymer composition may also be used as a coating on substrates, such as metal and ceramics, or may be used for spinning fibers. Precursors for forming such polymer compositions are also disclosed.

  12. PREDICTION OF THE RHEOLOGICAL PROPERTIES OF STAR-TYPE BRANCHED POLYMER SOLUTIONS BY MEANS OF THE FIXED SPECTRUM MODEL

    Institute of Scientific and Technical Information of China (English)

    WU Qiye

    1995-01-01

    The Rouse-Zimm model with slippage was improved and the basic parameters of modelwere modified to explain the rheological properties of star-type branched polymersolutions. The theoretical results show good agreement with experimental data.

  13. Modelling polymer draft gears

    Science.gov (United States)

    Wu, Qing; Yang, Xiangjian; Cole, Colin; Luo, Shihui

    2016-09-01

    This paper developed a new and simple approach to model polymer draft gears. Two types of polymer draft gears were modelled and compared with experimental data. Impact characteristics, in-train characteristics and frequency responses of these polymer draft gears were studied and compared with those of a friction draft gear. The impact simulations show that polymer draft gears can withstand higher impact speeds than the friction draft gear. Longitudinal train dynamics simulations show that polymer draft gears have significantly longer deflections than friction draft gears in normal train operations. The maximum draft gear working velocities are lower than 0.2 m/s, which are significantly lower than the impact velocities during shunting operations. Draft gears' in-train characteristics are similar to their static characteristics but are very different from their impact characteristics; this conclusion has also been reached from frequency response simulations. An analysis of gangway bridge plate failures was also conducted and it was found that they were caused by coupler angling behaviour and long draft gear deflections.

  14. Enzyme- and pH-Sensitive Branched Polymer-Doxorubicin Conjugate-Based Nanoscale Drug Delivery System for Cancer Therapy.

    Science.gov (United States)

    Wei, Xiaoli; Luo, Qiang; Sun, Ling; Li, Xue; Zhu, Hongyan; Guan, Pujun; Wu, Min; Luo, Kui; Gong, Qiyong

    2016-05-11

    Owing to their dendritic architectural features, branched copolymers have been investigated as drug delivery systems. In this paper, an enzyme- and pH-sensitive branched poly[N-(2-hydroxypropyl)methacrylamide] (polyHPMA) copolymer-doxorubicin (DOX) conjugate possessing a molecular weight (MW) of 165 kDa was designed and prepared via a one-pot reaction and drug conjugation. This conjugate's potential as a smart, nanoscale drug delivery system (NDDS) is also investigated. The branched conjugate was capable of forming nanoparticles with a negative surface charge. The self-assembled nanoparticles were 102 nm in diameter as measured by dynamic light scattering (DLS) and 95 nm in diameter via scanning electron microscopy, respectively. The nanoparticles were degraded to low-MW products (23∼25 kDa) in the presence of papain or cathepsin B, and the degradation was monitored via DLS and size-exclusion chromatography. The nanoparticles demonstrated pH-sensitive drug release, as the DOX was attached to the branched copolymer via a hydrazone bond. In comparison to free DOX, the conjugate-based nanoparticles exhibited greater accumulation in breast tumors, resulting in enhanced antitumor therapeutic indexes. Furthermore, widespread dissemination of the conjugate among breast tumor cells was confirmed by immunohistochemical assay. Finally, no obvious systemic toxicities were observed in vivo in normal mice. Thus, the branched HPMA copolymer-DOX conjugate may be employed as a safe and efficient pH- and enzyme-responsive NDDS for cancer therapy. PMID:27102364

  15. Enhancement of Polymer Cytocompatibility by Nanostructuring of Polymer Surface

    OpenAIRE

    Petr Slepička; Nikola Slepičková Kasálková; Lucie Bačáková; Zdeňka Kolská; Václav Švorčík

    2012-01-01

    Polymers with their advantageous physical, chemical, mechanical, and electrical properties and easy manufacturing are widely used in biology, tissue engineering, and medicine, for example, as prosthetic materials. In some cases the polymer usage may be impeded by low biocompatibility of common synthetic polymers. The biocompatibility can be improved by modification of polymer surface, for example, by plasma discharge, irradiation with ionizing radiation, and sometime subsequent grafting with ...

  16. Optimization of Polymer Separation by Gradient Polymer Elution Chromatography

    OpenAIRE

    Liem, Gideon R; Wang, Linda Nien-Hwa

    2013-01-01

    High Performance Liquid Chromatography (HPLC) has been a versatile separation method for polymers for many years. Analysis of different polymers by HPLC is typically done by utilizing the differential solubility of the polymers by mixing a good solvent and an anti-solvent in various compositions. This method is called Gradient Polymer Elution Chromatography (GPEC). While GPEC has been used extensively, it commonly uses a linear gradient to separate components. Linear solvent gradients consume...

  17. Polymer Photovoltaic Cells

    Institute of Scientific and Technical Information of China (English)

    Jianhui Hou; Chunhe Yang; Erjun Zhou; Chang He; Zhan'ao Tan; Youjun He; Yongfang Li

    2005-01-01

    @@ 1Introduction Polymer photovoltaic cells (PPVCs) have attracted much attention recently because of its easy fabrication, low cost and possibility to make flexible devices[1]. PPVC is composed of a conjugated polymer/C60blend layer (photosensitive layer) sandwiched between a transparent ITO electrode and a metal electrode.When a light through ITO electrode irradiates on the photosensitive layer, the photons with appropriate energy will be absorbed by the conjugated polymer (CP) and excitons (electron-hole pair) are produced. The excitons move to the interface of CP/C60 where the electrons transfer to the LUMO of C60 and holes leave on the HOMO of the CP. The separated electrons migrate through the C60 network to and are collected by the metal electrode, and the holes migrate through the CP network to and are collected by the ITO electrode, so that the photocurrent and photovoltage are attained.

  18. Antithrombogenic Polymer Coating.

    Science.gov (United States)

    Huang, Zhi Heng; McDonald, William F.; Wright, Stacy C.; Taylor, Andrew C.

    2003-01-21

    An article having a non-thrombogenic surface and a process for making the article are disclosed. The article is formed by (i) coating a polymeric substrate with a crosslinked chemical combination of a polymer having at least two amino substituted side chains, a crosslinking agent containing at least two crosslinking functional groups which react with amino groups on the polymer, and a linking agent containing a first functional group which reacts with a third functional group of the crosslinking agent, and (ii) contacting the coating on the substrate with an antithrombogenic agent which covalently bonds to a second functional group of the linking agent. In one example embodiment, the polymer is a polyamide having amino substituted alkyl chains on one side of the polyamide backbone, the crosslinking agent is a phosphine having the general formula (A).sub.3 P wherein A is hydroxyalkyl, the linking agent is a polyhydrazide and the antithrombogenic agent is heparin.

  19. 'Stuffed' conducting polymers

    DEFF Research Database (Denmark)

    Winther-Jensen, Bjørn; Chen, Jun; West, Keld;

    2005-01-01

    Conducting polymers (CP) obtained by oxidative polymerization using iron(III) salts shrink when Fe(II) and the excess counter ions are washed out after polymerization. This phenomenon can be used to incorporate active molecules into the CP matrix via their addition to the wash liquid. In the pres......Conducting polymers (CP) obtained by oxidative polymerization using iron(III) salts shrink when Fe(II) and the excess counter ions are washed out after polymerization. This phenomenon can be used to incorporate active molecules into the CP matrix via their addition to the wash liquid....... In the present work we demonstrate this principle on three different CP's: polypyrrole (PPy), poly-terthiophene (PTTh) and poly(3,4-ethylenedioxy thiophene) (PEDT), using ferrocene as a model molecule to be trapped in the polymer films. (c) 2005 Elsevier Ltd. All rights reserved....

  20. Semi-metallic polymers

    DEFF Research Database (Denmark)

    Bubnova, Olga; Khan, Zia Ullah; Wang, Hui;

    2014-01-01

    Polymers are lightweight, flexible, solution-processable materials that are promising for low-cost printed electronics as well as for mass-produced and large-area applications. Previous studies demonstrated that they can possess insulating, semiconducting or metallic properties; here we report...... that polymers can also be semi-metallic. Semi-metals, exemplified by bismuth, graphite and telluride alloys, have no energy bandgap and a very low density of states at the Fermi level. Furthermore, they typically have a higher Seebeck coefficient and lower thermal conductivities compared with metals, thus being...... a Fermi glass to a semi-metal. The high Seebeck value, the metallic conductivity at room temperature and the absence of unpaired electron spins makes polymer semi-metals attractive for thermoelectrics and spintronics....

  1. Protein Polymers and Amyloids

    DEFF Research Database (Denmark)

    Risør, Michael Wulff

    2014-01-01

    that inhibits its target protease through a large conformational change but mutations compromise this function and cause premature structural collapse into hyperstable polymers. Understanding the conformational disorders at a molecular level is not only important for our general knowledge on protein folding...... of this mechanism were investigated through a series of interaction experiments. Despite a very buried location in the native structure, evidence here suggest that the C-terminal tail is labile under slightly destabilizing conditions, providing new detail to this matter. A small infectious polymer unit was also...... constructed and used to show how polymerogenic seeding and polymer propagation might happen inside the body. The locking of central structural elements during α1AT folding or in the native state represents a therapeutic strategy to prevent polymerization. Using Molecular Dynamics simulations, we identified...

  2. Active Polymer Gel Actuators

    Directory of Open Access Journals (Sweden)

    Shuji Hashimoto

    2010-01-01

    Full Text Available Many kinds of stimuli-responsive polymer and gels have been developed and applied to biomimetic actuators or artificial muscles. Electroactive polymers that change shape when stimulated electrically seem to be particularly promising. In all cases, however, the mechanical motion is driven by external stimuli, for example, reversing the direction of electric field. On the other hand, many living organisms can generate an autonomous motion without external driving stimuli like self-beating of heart muscles. Here we show a novel biomimetic gel actuator that can walk spontaneously with a wormlike motion without switching of external stimuli. The self-oscillating motion is produced by dissipating chemical energy of oscillating reaction. Although the gel is completely composed of synthetic polymer, it shows autonomous motion as if it were alive.

  3. Acoustomechanics of semicrystalline polymers

    Directory of Open Access Journals (Sweden)

    Fengxian Xin

    2016-01-01

    Full Text Available We develop an acoustomechanical theory for semicrystalline polymers and demonstrate that acoustic radiation force is capable of causing giant deformation in these materials. When a polymer layer is subjected to combined tensile mechanical force in plane and acoustic force (sound pressure through thickness, it becomes initially homogeneously thin but soon inhomogeneous when the two forces reach critical conditions. Critical conditions for such acoustomechanical instability are theoretically determined based on the J2-deformation theory. We demonstrate that pull-in instability can be acoustically triggered even if the in-plane mechanical force is fixed. Bifurcation in the critical condition for acoustomechanical instability occurs when the polymer exhibits sufficiently large hardening. The findings of this study enable reliability design of novel acoustic actuated devices.

  4. Toxicology of Biomedical Polymers

    Directory of Open Access Journals (Sweden)

    P. V. Vedanarayanan

    1987-04-01

    Full Text Available This paper deals with the various types of polymers, used in the fabrication of medical devices, their diversity of applications and toxic hazards which may arise out of their application. The potential toxicity of monomers and the various additives used in the manufacture of biomedical polymers have been discussed along with hazards which may arise out of processing of devices such as sterilization. The importance of quality control and stringent toxicity evaluation methods have been emphasised since in our country, at present, there are no regulations covering the manufacturing and marketing of medical devices. Finally the question of the general and subtle long term systemic toxicity of biomedical polymers have been brought to attention with the suggestion that this question needs to be resolved permanently by appropriate studies.

  5. Polymers and colloids

    Energy Technology Data Exchange (ETDEWEB)

    Schurtenberger, P. [ETH Zurich, Inst. fuer Polymere, Zurich (Switzerland)

    1996-11-01

    A wealth of structural information from colloid and polymer solutions on a large range of length scales can be obtained using small angle neutron scattering (SANS) experiments. After a general introduction to the field of soft condensed matter, I shall give a few selected examples on how SANS combined with suitable contrast variation schemes can be used to extract information on the size and conformation of polymer coils in solution and in the melt, and on the local structure and flexibility of polymerlike micelles and microemulsions. (author) 8 figs., tabs., 44 refs.

  6. Delocalization in polymer models

    CERN Document Server

    Jitomirskaya, S Yu; Stolz, G

    2003-01-01

    A polymer model is a one-dimensional Schroedinger operator composed of two finite building blocks. If the two associated transfer matrices commute, the corresponding energy is called critical. Such critical energies appear in physical models, an example being the widely studied random dimer model. Although the random models are known to have pure-point spectrum with exponentially localized eigenstates for almost every configuration of the polymers, the spreading of an initially localized wave packet is here proven to be at least diffusive for every configuration.

  7. Polymers at cryogenic temperatures

    CERN Document Server

    Fu, Shao-Yun

    2013-01-01

    Kalia and Fu's novel monograph covers cryogenic treatment, properties and applications of cryo-treated polymer materials. Written by numerous international experts, the twelve chapters in this book offer the reader a comprehensive picture of the latest findings and developments, as well as an outlook on the field. Cryogenic technology has seen remarkable progress in the past few years and especially cryogenic properties of polymers are attracting attention through new breakthroughs in space, superconducting, magnetic and electronic techniques. This book is a valuable resource for researchers, educators, engineers and graduate students in the field and at technical institutions.

  8. Shape memory polymer foams

    Science.gov (United States)

    Santo, Loredana

    2016-02-01

    Recent advances in shape memory polymer (SMP) foam research are reviewed. The SMPs belong to a new class of smart polymers which can have interesting applications in microelectromechanical systems, actuators and biomedical devices. They can respond to specific external stimulus changing their configuration and then remember the original shape. In the form of foams, the shape memory behaviour can be enhanced because they generally have higher compressibility. Considering also the low weight, and recovery force, the SMP foams are expected to have great potential applications primarily in aerospace. This review highlights the recent progress in characterization, evaluation, and proposed applications of SMP foams mainly for aerospace applications.

  9. Nanoparticles from Renewable Polymers

    Directory of Open Access Journals (Sweden)

    Frederik Roman Wurm

    2014-07-01

    Full Text Available The use of polymers from natural resources can bring many benefits for novel polymeric nanoparticle systems. Such polymers have a variety of beneficial properties such as biodegradability and biocompatibility, they are readily available on large scale and at low cost. As the amount of fossil fuels decrease, their application becomes more interesting even if characterization is in many cases more challenging due to structural complexity, either by broad distribution of their molecular weights polysaccharides, polyesters, lignin or by complex structure (proteins, lignin. This review summarizes different sources and methods for the preparation of biopolymer-based nanoparticle systems for various applications.

  10. Antibacterial polymer coatings.

    Energy Technology Data Exchange (ETDEWEB)

    Wilson, Mollye C.; Allen, Ashley N.; Barnhart, Meghan; Tucker, Mark David; Hibbs, Michael R.

    2009-09-01

    A series of poly(sulfone)s with quaternary ammonium groups and another series with aldehyde groups are synthesized and tested for biocidal activity against vegetative bacteria and spores, respectively. The polymers are sprayed onto substrates as coatings which are then exposed to aqueous suspensions of organisms. The coatings are inherently biocidal and do not release any agents into the environment. The coatings adhere well to both glass and CARC-coated coupons and they exhibit significant biotoxicity. The most effective quaternary ammonium polymers kills 99.9% of both gram negative and gram positive bacteria and the best aldehyde coating kills 81% of the spores on its surface.

  11. Edible Polymers: Challenges and Opportunities

    Directory of Open Access Journals (Sweden)

    Subhas C. Shit

    2014-01-01

    Full Text Available Edible polymers have established substantial deliberation in modern eons because of their benefits comprising use as edible materials over synthetic polymers. This could contribute to the reduction of environmental contamination. Edible polymers can practically diminish the complexity and thus improve the recyclability of materials, compared to the more traditional non-environmentally friendly materials and may be able to substitute such synthetic polymers. A synthetic hydrogel polymer unlocked a new possibility for development of films, coatings, extrudable pellets, and synthetic nanopolymers, particularly designed for medical, agricultural, and industrial fields. Edible polymers offer many advantages for delivering drugs and tissue engineering. Edible polymer technology helps food industries to make their products more attractive and safe to use. Novel edible materials have been derived from many natural sources that have conventionally been regarded as discarded materials. The objective of this review is to provide a comprehensive introduction to edible polymers by providing descriptions in terms of their origin, properties, and potential uses.

  12. Synthetic Metal-Containing Polymers

    Science.gov (United States)

    Manners, Ian

    2004-04-01

    The development of the field of synthetic metal-containing polymers - where metal atoms form an integral part of the main chain or side group structure of a polymer - aims to create new materials which combine the processability of organic polymers with the physical or chemical characteristics associated with the metallic element or complex. This book covers the major developments in the synthesis, properties, and applications of synthetic metal-containing macromolecules, and includes chapters on the preparation and characterization of metal-containing polymers, metallocene-based polymers, rigid-rod organometallic polymers, coordination polymers, polymers containing main group metals, and also covers dendritic and supramolecular systems. The book describes both polymeric materials with metals in the main chain or side group structure and covers the literature up to the end of 2002.

  13. Composite solid polymer electrolyte membranes

    Energy Technology Data Exchange (ETDEWEB)

    Formato, Richard M. (Shrewsbury, MA); Kovar, Robert F. (Wrentham, MA); Osenar, Paul (Watertown, MA); Landrau, Nelson (Marlborough, MA); Rubin, Leslie S. (Newton, MA)

    2001-06-19

    The present invention relates to composite solid polymer electrolyte membranes (SPEMs) which include a porous polymer substrate interpenetrated with an ion-conducting material. SPEMs of the present invention are useful in electrochemical applications, including fuel cells and electrodialysis.

  14. Hydrothermal synthesis of nanostructured hybrids based on iron oxide and branched PEI polymers. Influence of high pressure on structure and morphology

    Energy Technology Data Exchange (ETDEWEB)

    Popescu, L.M., E-mail: mpopescu@imnr.ro [National R& D Institute for Non-ferrous and Rare Metals, 102 Biruintei Blvd, Pantelimon, Judetul Ilfov (Romania); Piticescu, R.M., E-mail: roxana@imnr.ro [National R& D Institute for Non-ferrous and Rare Metals, 102 Biruintei Blvd, Pantelimon, Judetul Ilfov (Romania); Petriceanu, M., E-mail: mirelap@imnr.ro [National R& D Institute for Non-ferrous and Rare Metals, 102 Biruintei Blvd, Pantelimon, Judetul Ilfov (Romania); Ottaviani, M.F., E-mail: maria.ottaviani@uniurb.it [University of Urbino “Carlo Bo”, Department of Earth, Life and Environmental Sciences, Urbino (Italy); Cangiotti, M., E-mail: michela.cangiotti@uniurb.it [University of Urbino “Carlo Bo”, Department of Earth, Life and Environmental Sciences, Urbino (Italy); Vasile, E., E-mail: eugeniuvasile@yahoo.com [University Politehnica of Bucharest, Bucharest (Romania); National R& D Institute for Non-ferrous and Rare Metals, 102 Biruintei Blvd, Pantelimon, Judetul Ilfov (Romania); Dîrtu, M.M., E-mail: marinela.dirtu@uclouvain.be [Institute of Condensed Mater and Nanosciences, Molecules, Solids and Reactivity (IMCN/MOST), Université Catholique de Louvain, Place L. Pasteur 1, 1348 Louvain-la-Neuve (Belgium); Wolff, M., E-mail: mariusz.wolff@uclouvain.be [Institute of Condensed Mater and Nanosciences, Molecules, Solids and Reactivity (IMCN/MOST), Université Catholique de Louvain, Place L. Pasteur 1, 1348 Louvain-la-Neuve (Belgium); Garcia, Y., E-mail: yann.garcia@uclouvain.be [Institute of Condensed Mater and Nanosciences, Molecules, Solids and Reactivity (IMCN/MOST), Université Catholique de Louvain, Place L. Pasteur 1, 1348 Louvain-la-Neuve (Belgium); and others

    2015-07-01

    Homogeneous hybrids in which iron oxide nanoparticles are entrapped within polymer structure are of interest for their potential applications in biomedical field, such as diagnostic, therapeutic and theranostic purposes. For this reason, hybrid nanomaterials based on branched polyethyleneimine (PEI) and iron oxide with different ratios were synthesized in a single step by hydrothermal procedure at high pressure and low temperature. Iron oxide is formed in the presence of branched PEI and the interaction between them takes place in the reaction medium. The influence of synthesis parameters on the hybrid formation, as well as chemical and structural properties was studied by means of FTIR, DSC-TG, HRTEM, electron paramagnetic resonance (EPR), magnetic measurements (SQUID) and {sup 57}Fe Mössbauer analyses. It has been shown that synthesis parameters influence thermal stability and morphology of the hybrids. FeO(OH) crystallites of 2–5 nm are formed. Iron oxyhydroxide nanoparticles strongly entrapped in PEI structure are obtained. The low and distributed values of the specific spontaneous magnetisation in samples prepared under the same pressure conditions support the presence of very fine FeO(OH) nanoparticles, which formation and magnetic properties are depending on the mass ratio between iron oxide and PEI. - Highlights: • Polyethyleneimine (PEI) – iron oxide hybrids were synthesized by hydrothermal method. • Synthesis parameters influence thermal stability and morphology of the hybrids. • Small crystallites of FeO(OH) with size between 2 and 5 nm are formed. • Formation of stable hybrid nanostructures in the pressure range 1000–3000 atm. • FeO(OH) nanoparticles are entrapped in PEI structure at low inorganic–organic ratio.

  15. Polymer-solvent molecular compounds

    CERN Document Server

    Guenet, Jean-Michel

    2010-01-01

    Crystallisable polymers represent a large share of the polymers used for manufacturing a wide variety of objects, and consequently have received continuous attention from scientists these past 60 years. Molecular compounds from crystallisable polymers, particularly from synthetic polymers, are receiving growing interest due to their potential application in the making of new materials such as multiporous membranes capable of capturing large particles as well as small pollutant molecules. The present book gives a detailed description of these promising systems. The first chapter

  16. Shape memory polymer medical device

    Science.gov (United States)

    Maitland, Duncan; Benett, William J.; Bearinger, Jane P.; Wilson, Thomas S.; Small, IV, Ward; Schumann, Daniel L.; Jensen, Wayne A.; Ortega, Jason M.; Marion, III, John E.; Loge, Jeffrey M.

    2010-06-29

    A system for removing matter from a conduit. The system includes the steps of passing a transport vehicle and a shape memory polymer material through the conduit, transmitting energy to the shape memory polymer material for moving the shape memory polymer material from a first shape to a second and different shape, and withdrawing the transport vehicle and the shape memory polymer material through the conduit carrying the matter.

  17. Polymer Thermoelectric Generators: Device Considerations

    Science.gov (United States)

    Yee, Shannon

    2014-03-01

    Recent control of the transport properties in polymers has encouraged the development of polymer thermoelectric (TE) devices. Polymer TEs are thought to be less expensive and more scalable than their inorganic counterparts. The cost of the raw material is less and polymer TEs can leverage the large areal manufacturing technique established by the plastics industry. Additionally, while the overall ZT of polymer TEs appears attractive, individual polymer properties have a very different scale than their inorganic counterparts (i.e., the thermal conductivity and electrical conductivity are approximately one and two orders of magnitude smaller, respectively). Furthermore, the majority of TE measurements on polymers have been limited to thin-films where traditional TE materials are measured in bulk. So why should it be expected that polymer TE devices resemble traditional TE devices? Given the uniqueness of polymers, different device architectures are proposed that can leverage the unique strengths of polymer films. It will be shown that by logically considering device requirements, new polymer TE devices have non-linear features that are more attractive than linear inorganic TE devices. This leads to very different device optimizations that favor polymer TEs.

  18. Adsorption theory for polydisperse polymers.

    NARCIS (Netherlands)

    Roefs, S.P.F.M.; Scheutjens, J.M.H.M.; Leermakers, F.A.M.

    1994-01-01

    Most polymers are polydisperse. We extend the self-consistent field polymer adsorption theory due to Scheutjens and Fleer to account for an arbitrary polymer molecular weight distribution with a cutoff chain length Nmax. In this paper, the treatment is restricted to homopolymers. For this case a ver

  19. Polymer modification via. cluster formation

    International Nuclear Information System (INIS)

    Ion beam treatment studies have been carried out to investigate the potential for improvements in conductivity properties of the polymers. Change in polymer stoichiometry were characterised by investigating into the carbon clusters formed along the latent tracks of energetic ions in polymers. Here we present some new results which have been derived from UV-Vis spectroscopic examinations. (author)

  20. Aerogel/polymer composite materials

    Science.gov (United States)

    Williams, Martha K. (Inventor); Smith, Trent M. (Inventor); Fesmire, James E. (Inventor); Roberson, Luke B. (Inventor); Clayton, LaNetra M. (Inventor)

    2010-01-01

    The invention provides new composite materials containing aerogels blended with thermoplastic polymer materials at a weight ratio of aerogel to thermoplastic polymer of less than 20:100. The composite materials have improved thermal insulation ability. The composite materials also have better flexibility and less brittleness at low temperatures than the parent thermoplastic polymer materials.

  1. Viscoelastic Properties of Polymer Blends

    Science.gov (United States)

    Hong, S. D.; Moacanin, J.; Soong, D.

    1982-01-01

    Viscosity, shear modulus and other viscoelastic properties of multicomponent polymer blends are predicted from behavior of individual components, using a mathematical model. Model is extension of two-component-blend model based on Rouse-Bueche-Zimm theory of polymer viscoelasticity. Extension assumes that probabilities of forming various possible intracomponent and intercomponent entanglements among polymer molecules are proportional to relative abundances of components.

  2. Nonlinear microstructured polymer optical fibres

    DEFF Research Database (Denmark)

    Frosz, Michael Henoch

    is potentially the case for microstructured polymer optical fibres (mPOFs). Another advantage is that polymer materials have a higher biocompatibility than silica, meaning that it is easier to bond certain types of biosensor materials to a polymer surface than to silica. As with silica PCFs, it is difficult...

  3. Influence of Molecular Solvation on the Conformation of Star Polymers

    CERN Document Server

    Li, Xin; Sánchez-Diáz, Luis E; Do, Changwoo; Liu, Yun; Kim, Tae-Hwan; Smith, Gregory S; Hamilton, William A; Hong, Kunlun; Chen, Wei-Ren

    2014-01-01

    We have used neutron scattering to investigate the influence of concentration on the conformation of a star polymer. By varying the contrast between the solvent and isotopically labeled stars, we obtain the distributions of polymer and solvent within a star polymer from analysis of scattering data. A correlation between the local desolvation and the inward folding of star branches is discovered. From the perspective of thermodynamics, we find an analogy between the mechanism of polymer localization driven by solvent depletion and that of the hydrophobic collapse of polymers in solutions.

  4. Partial structure factors in star polymer/colloid mixtures

    CERN Document Server

    Stellbrink, J; Richter, D; Moussaid, A; Schofield, A B; Poon, W C K; Pusey, P N; Lindner, P; Dzubiella, J; Likos, C N; Löwen, H

    2002-01-01

    Addition of polymer to colloidal suspensions induces an attractive part to the colloid pair potential, which is of purely entropic origin (''depletion interaction''). We investigated the influence of polymer branching on depletion forces by studying mixtures of hard sphere colloids and star polymers with increasing arm number f=2-32, but constant R sub g approx 500 A. We found a pronounced effect of branching on the position of the gas/liquid demixing transition. Using small angle neutron scattering (SANS) we were able to measure partial structure factors in star polymer/colloid mixtures. The relative distance to the demixing transition is reflected in our scattering data. (orig.)

  5. Segmented conjugated polymers

    Indian Academy of Sciences (India)

    G Padmanaban; S Ramakrishnan

    2003-08-01

    Segmented conjugated polymers, wherein the conjugation is randomly truncated by varying lengths of non-conjugated segments, form an interesting class of polymers as they not only represent systems of varying stiffness, but also ones where the backbone can be construed as being made up of chromophores of varying excitation energies. The latter feature, especially when the chromophores are fluorescent, like in MEHPPV, makes these systems particularly interesting from the photophysics point of view. Segmented MEHPPV- samples, where x represents the mole fraction of conjugated segments, were prepared by a novel approach that utilizes a suitable precursor wherein selective elimination of one of the two eliminatable groups is affected; the uneliminated units serve as conjugation truncations. Control of the composition x of the precursor therefore permits one to prepare segmented MEHPPV- samples with varying levels of conjugation (elimination). Using fluorescence spectroscopy, we have seen that even in single isolated polymer chains, energy migration from the shorter (higher energy) chromophores to longer (lower energy) ones occurs – the extent of which depends on the level of conjugation. Further, by varying the solvent composition, it is seen that the extent of energy transfer and the formation of poorly emissive inter-chromophore excitons are greatly enhanced with increasing amounts of non-solvent. A typical S-shaped curve represents the variation of emission yields as a function of composition suggestive of a cooperative collapse of the polymer coil, reminiscent of conformational transitions seen in biological macromolecules.

  6. Phosphazene Polymers Containing Carborane

    Science.gov (United States)

    Fewell, L. L.; Parker, J. A.; Basi, R. J.

    1986-01-01

    Addition of carborane increases thermal stability. Carborane-substituted polyphosphazenes prepared by thermal polymerization of phenylcarbonyl-pentachlorocyclotriphosphazene followed by reaction with sodium trifluoroethoxide to replace remaining chlorine atoms with trifluoroethoxy groups. Improved polymers offer high char yields and resistance to hydrolysis.

  7. Cyclic polymers from alkynes

    Science.gov (United States)

    Roland, Christopher D.; Li, Hong; Abboud, Khalil A.; Wagener, Kenneth B.; Veige, Adam S.

    2016-08-01

    Cyclic polymers have dramatically different physical properties compared with those of their equivalent linear counterparts. However, the exploration of cyclic polymers is limited because of the inherent challenges associated with their synthesis. Conjugated linear polyacetylenes are important materials for electrical conductivity, paramagnetic susceptibility, optical nonlinearity, photoconductivity, gas permeability, liquid crystallinity and chain helicity. However, their cyclic analogues are unknown, and therefore the ability to examine how a cyclic topology influences their properties is currently not possible. We have solved this challenge and now report a tungsten catalyst supported by a tetraanionic pincer ligand that can rapidly polymerize alkynes to form conjugated macrocycles in high yield. The catalyst works by tethering the ends of the polymer to the metal centre to overcome the inherent entropic penalty of cyclization. Gel-permeation chromatography, dynamic and static light scattering, viscometry and chemical tests are all consistent with theoretical predictions and provide unambiguous confirmation of a cyclic topology. Access to a wide variety of new cyclic polymers is now possible by simply choosing the appropriate alkyne monomer.

  8. Metal-Polymer Nanocomposites

    Science.gov (United States)

    Nicolais, Luigi; Carotenuto, Gianfranco

    2004-09-01

    A unique guide to an essential area of nanoscience Interest in nano-sized metals has increased greatly due to their special characteristics and suitability for a number of advanced applications. As technology becomes more refined-including the ability to effectively manipulate and stabilize metals at the nanoscale-these materials present ever-more workable solutions to a growing range of problems. Metal-Polymer Nanocomposites provides the first guide solely devoted to the unique properties and applications of this essential area of nanoscience. It offers a truly multidisciplinary approach, making the text accessible to readers in physical, chemical, and materials science as well as areas such as engineering and topology. The thorough coverage includes: * The chemical and physical properties of nano-sized metals * Different approaches to the synthesis of metal-polymer nanocomposites (MPN) * Advanced characterization techniques and methods for study of MPN * Real-world applications, including color filters, polarizers, optical sensors, nonlinear optical devices, and more * An extensive list of references on the topics covered A unique, cutting-edge resource for a vital area of nanoscience development, Metal-Polymer Nanocomposites is an invaluable text for students and practitioners of materials science, engineering, polymer science, chemical engineering, electrical engineering, and optics.

  9. Mechanically Invisible Polymer Coatings

    DEFF Research Database (Denmark)

    2014-01-01

    The present invention relates to a composition comprising encapsulated particles in a polymeric material. The composition comprises a continuous phase and a discontinuous phase incorporated therein, wherein the continuous phase comprises a first polymeric material and wherein the discontinuous ph...... invisible polymer coatings....

  10. Conformational properties of polymers

    Indian Academy of Sciences (India)

    A R Singh; D Giri; S Kumar

    2008-08-01

    We discuss exact enumeration technique and its application to polymers and biopolymers. Using this method one can obtain phase diagram in thermodynamic limit. The method works quite well in describing the outcomes of single molecule force spectroscopy results where finite size effects play a crucial role.

  11. Self-sterilizing polymers

    Science.gov (United States)

    Tulis, J. J.; Daley, D. J.; Phillips, G. B.

    1973-01-01

    Addition of approximately 1% paraformaldehyde to room-temperature-vulcanizing potting polymer results in effective, controllable germicide. When heated above ambient temperatures, paraformaldehyde releases dry formaldehyde, which can penetrate enclosed areas and packages, will not damage material, and leaves no permanent residue.

  12. Transferases in Polymer Chemistry

    NARCIS (Netherlands)

    van der Vlist, Jeroen; Loos, Katja; Palmans, ARA; Heise, A

    2010-01-01

    Transferases are enzymes that catalyze reactions in which a group is transferred from one compound to another. This makes these enzymes ideal catalysts for polymerization reactions. In nature, transferases are responsible for the synthesis of many important natural macromolecules. In synthetic polym

  13. The use of azide-alkyne click chemistry in recent syntheses and applications of polytriazole-based nanostructured polymers

    Science.gov (United States)

    Shi, Yi; Cao, Xiaosong; Gao, Haifeng

    2016-02-01

    The rapid development of efficient organic click coupling reactions has significantly facilitated the construction of synthetic polymers with sophisticated branched nanostructures. This Feature Article summarizes the recent progress in the application of efficient copper-catalyzed and copper-free azide-alkyne cycloaddition (CuAAC and CuFAAC) reactions in the syntheses of dendrimers, hyperbranched polymers, star polymers, graft polymers, molecular brushes, and cyclic graft polymers. Literature reports on the interesting properties and functions of these polytriazole-based nanostructured polymers are also discussed to illustrate their potential applications as self-healing polymers, adhesives, polymer catalysts, opto-electronic polymer materials and polymer carriers for drug and imaging molecules.

  14. Dynamics of Polaron at Polymer/Polymer Interface

    Institute of Scientific and Technical Information of China (English)

    DI Bing; MENG Yan; AN Zhong; LI You-Cheng

    2008-01-01

    The migration of a polaron at polymer/polymer interface is believed to be of fundamental importance for the transport and light-emitting properties of conjugated polymer-based light emitting diodes.Based on the onedimensional tight-binding Su-Schrieffer-Heeger(SSH)model,we have investigated polaron dynamics in a onedimensional polymer/polymer system by using a nonadiabatic evolution method.In particular,we focus on how a polaron migrates through the conjugated polymer/polymer interface in the presence of external electric field.The results show that the migration of polaron at the interface depends sensitively on the hopping integrals,the potential barrier induced by the energy mismatch,and the strength of applied electric field which increases the polaron kinetic energy.

  15. POLYMER ELECTROLYTE MEMBRANE FUEL CELLS

    DEFF Research Database (Denmark)

    2001-01-01

    thermoplastic polymers for high temperature polymer electrolyte fuel cells have also been developed. Miscible blends are used for solution casting of polymer membranes (solid electrolytes). High conductivity and enhanced mechanical strength were obtained for the blend polymer solid electrolytes....... With the thermally resistant polymer, e.g., polybenzimidazole or a mixture of polybenzimidazole and other thermoplastics as binder, the carbon-supported noble metal catalyst is tape-cast onto a hydrophobic supporting substrate. When doped with an acid mixture, electrodes are assembled with an acid doped solid...

  16. Frictional properties of confined polymers

    DEFF Research Database (Denmark)

    Sivebæk, Ion Marius; Samoilov, Vladimir N; Persson, Bo N J

    2008-01-01

    We present molecular dynamics friction calculations for confined hydrocarbon solids with molecular lengths from 20 to 1400 carbon atoms. Two cases are considered: a) polymer sliding against a hard substrate, and b) polymer sliding on polymer. In the first setup the shear stresses are relatively...... independent of molecular length. For polymer sliding on polymer the friction is significantly larger, and dependent on the molecular chain length. In both cases, the shear stresses are proportional to the squeezing pressure and finite at zero load, indicating an adhesional contribution to the friction force...

  17. A Modified Polymer from Polyacrylonitrile

    Directory of Open Access Journals (Sweden)

    Indra Bajaj

    1969-07-01

    Full Text Available Polyacrylonitrile has been modified by introducing thioamide groups (-CSNH/sub 2/ in place of nitride groups (-CN in the chain by passing dry H/sub 2/ S gas through a 5% solution of the polymer in N-N dimethylformamide. The modified polymer is soluble in acetone. X-ray study revealed the complete loss of crystallinity in the modified polymer. Infra-red spectrum of the polymer film shows strong absorption bands at 3390 cm/sup 1/, 2273 cm/sup 1/ and 1667 cm/sup 1/ indicating the presence of both thioamide and nitride groups in the polymer chain.

  18. Conducting Polymers for Neutron Detection

    Energy Technology Data Exchange (ETDEWEB)

    Kimblin, Clare; Miller, Kirk; Vogel, Bob; Quam, Bill; McHugh, Harry; Anthony, Glen; Mike, Grover

    2007-12-01

    Conjugated polymers have emerged as an attractive technology for large-area electronic applications. As organic semiconductors, they can be used to make large-area arrays of diodes or transistors using fabrication techniques developed for polymer coatings, such as spraying and screen-printing. We have demonstrated both neutron and alpha detection using diodes made from conjugated polymers and have done preliminary work to integrate a boron carbide layer into the conventional polymer device structure to capture thermal neutrons. The polymer devices appear to be insensitive to gamma rays, due to their small physical thickness and low atomic number.

  19. Photogenerating work from polymers

    Directory of Open Access Journals (Sweden)

    Hilmar Koerner

    2008-07-01

    Full Text Available The ability to control the creation of mechanical work remotely, with high speed and spatial precision, over long distances, offers many intriguing possibilities. Recent developments in photoresponsive polymers and nanocomposite concepts are at the heart of these future devices. Whether driving direct conformational changes, initiating reversible chemical reactions to release stored strain, or converting a photon to a local temperature increase, combinations of photoactive units, nanoparticles, ordered mesophases, and polymeric networks are providing an expansive array of photoresponsive polymer options for mechanical devices. Framing the typically geometry-specific observations into an applied engineering vocabulary will ultimately define the role of these materials in future actuator applications, ranging from microfluidic valves in medical devices to optically controlled mirrors in displays.

  20. How do polymers degrade?

    Science.gov (United States)

    Lyu, Suping

    2011-03-01

    Materials derived from agricultural products such as cellulose, starch, polylactide, etc. are more sustainable and environmentally benign than those derived from petroleum. However, applications of these polymers are limited by their processing properties, chemical and thermal stabilities. For example, polyethylene terephthalate fabrics last for many years under normal use conditions, but polylactide fabrics cannot due to chemical degradation. There are two primary mechanisms through which these polymers degrade: via hydrolysis and via oxidation. Both of these two mechanisms are related to combined factors such as monomer chemistry, chain configuration, chain mobility, crystallinity, and permeation to water and oxygen, and product geometry. In this talk, we will discuss how these materials degrade and how the degradation depends on these factors under application conditions. Both experimental studies and mathematical modeling will be presented.

  1. Dielectric Actuation of Polymers

    Science.gov (United States)

    Niu, Xiaofan

    Dielectric polymers are widely used in a plurality of applications, such as electrical insulation, dielectric capacitors, and electromechanical actuators. Dielectric polymers with large strain deformations under an electric field are named dielectric elastomers (DE), because of their relative low modulus, high elongation at break, and outstanding resilience. Dielectric elastomer actuators (DEA) are superior to traditional transducers as a muscle-like technology: large strains, high energy densities, high coupling efficiency, quiet operation, and light weight. One focus of this dissertation is on the design of DE materials with high performance and easy processing. UV radiation curing of reactive species is studied as a generic synthesis methodology to provide a platform for material scientists to customize their own DE materials. Oligomers/monomers, crosslinkers, and other additives are mixed and cured at appropriate ratios to control the stress-strain response, suppress electromechanical instability of the resulting polymers, and provide stable actuation strains larger than 100% and energy densities higher than 1 J/g. The processing is largely simplified in the new material system by removal of the prestretching step. Multilayer stack actuators with 11% linear strain are demonstrated in a procedure fully compatible with industrial production. A multifunctional DE derivative material, bistable electroactive polymer (BSEP), is invented enabling repeatable rigid-to-rigid deformation without bulky external structures. Bistable actuation allows the polymer actuator to have two distinct states that can support external load without device failure. Plasticizers are used to lower the glass transition temperature to 45 °C. Interpenetrating polymer network structure is established inside the BSEP to suppress electromechanical instability, providing a breakdown field of 194 MV/m and a stable bistable strain as large as 228% with a 97% strain fixity. The application of BSEP

  2. Dynamics of polymers

    Energy Technology Data Exchange (ETDEWEB)

    Buchenau, U. [Forschungszentrum Juelich GmbH (Germany). Inst. fuer Energieverfahrenstechnik

    1996-11-01

    Neutron scattering from amorphous polymers allows to switch from incoherent to coherent scattering in the same substance. The power of the tool for the study of the picosecond dynamics of disordered matter is illustrated for polybutadiene, polycarbonate and polystyrene. The results suggest a mixture of sound waves and localized modes, strongly interacting with each other, in the picosecond range. (author) 8 figs., tabs., 39 refs.

  3. Dynamics of polymers

    International Nuclear Information System (INIS)

    Neutron scattering from amorphous polymers allows to switch from incoherent to coherent scattering in the same substance. The power of the tool for the study of the picosecond dynamics of disordered matter is illustrated for polybutadiene, polycarbonate and polystyrene. The results suggest a mixture of sound waves and localized modes, strongly interacting with each other, in the picosecond range. (author) 8 figs., tabs., 39 refs

  4. High performance polymer concrete

    OpenAIRE

    Frías, M.; San-José, J. T.

    2007-01-01

    This paper studies the performance of concrete whose chief components are natural aggregate and an organic binder —a thermosetting polyester resin— denominated polymer concrete or PC. The material was examined macro- and microscopically and its basic physical and mechanical properties were determined using mercury porosimetry, scanning electron microscopy (SEM-EDAX), X-ray diffraction (XRD) and strength tests (modulus of elasticity, stress-strain curves and ultimate strengths). A...

  5. Knots in polymers

    Indian Academy of Sciences (India)

    Yacov Kantov

    2005-06-01

    Knots and topological entanglements play an important role in the statistical mechanics of polymers. While topological entanglement is a global property, it is possible to study the size of a knotted region both numerically and analytically. It can be shown that long-range repulsive interactions, as well as entropy favor small knots in dilute systems. However, in dense systems and at the -point in two dimensions the uncontracted knot configuration is the most likely.

  6. Conjugated polymer nanoparticles

    Science.gov (United States)

    Tuncel, Dönüs; Demir, Hilmi Volkan

    2010-04-01

    Conjugated polymer nanoparticles are highly versatile nano-structured materials that can potentially find applications in various areas such as optoelectronics, photonics, bio-imaging, bio-sensing and nanomedicine. Their straightforward synthesis in desired sizes and properties, biocompatibility and non-toxicity make these materials highly attractive for the aforementioned applications. This feature article reviews the recent developments in the synthesis, characterization, properties and application of these exciting nanostructured materials.

  7. Electrochemical polymer electrolyte membranes

    CERN Document Server

    Fang, Jianhua; Wilkinson, David P

    2015-01-01

    Electrochemical Polymer Electrolyte Membranes covers PEMs from fundamentals to applications, describing their structure, properties, characterization, synthesis, and use in electrochemical energy storage and solar energy conversion technologies. Featuring chapters authored by leading experts from academia and industry, this authoritative text: Discusses cutting-edge methodologies in PEM material selection and fabricationPoints out important challenges in developing PEMs and recommends mitigation strategies to improve PEM performanceAnalyzes the cur

  8. Polymers in Fractal Disorder

    OpenAIRE

    Fricke, Niklas

    2016-01-01

    This work presents a numerical investigation of self-avoiding walks (SAWs) on percolation clusters, a canonical model for polymers in disordered media. A new algorithm has been developed allowing exact enumeration of over ten thousand steps. This is an increase of several orders of magnitude compared to previously existing enumeration methods, which allow for barely more than forty steps. Such an increase is achieved by exploiting the fractal structure of critical percolation clusters: they a...

  9. Mass transport in polymers

    OpenAIRE

    Ferrari, Maria Chiara

    2009-01-01

    The study of mass transport in polymeric membranes has grown in importance due to its potential application in many processes such as separation of gases and vapors, packaging, controlled drug release. The diffusion of a low molecular weight species in a polymer is often accompanied by other phenomena like swelling, reactions, stresses, that have not been investigated in all their aspects yet. Furthermore, novel materials have been developed that include inorganic fillers, reactive functional...

  10. Conductive Polymer Composites

    OpenAIRE

    Pierini, Filippo

    2013-01-01

    In recent years, nanotechnologies have led to the production of materials with new and sometimes unexpected qualities through the manipulation of nanoscale components. This research aimed primarily to the study of the correlation between hierarchical structures of hybrid organic-inorganic materials such as conductive polymer composites (CPCs). Using a bottom-up methodology, we could synthesize a wide range of inorganic nanometric materials with a high degree of homogeneity and purity, ...

  11. Absorbable and biodegradable polymers

    CERN Document Server

    Shalaby, Shalaby W

    2003-01-01

    INTRODUCTION NOTES: Absorbable/Biodegradable Polymers: Technology Evolution. DEVELOPMENT AND APPLICATIONOF NEW SYSTEMS: Segmented Copolyesters with Prolonged Strength Retention Profiles. Polyaxial Crystalline Fiber-Forming Copolyester. Polyethylene Glycol-Based Copolyesters. Cyanoacrylate-Based Systems as Tissue Adhesives. Chitosan-Based Systems. Hyaluronic Acid-Based Systems. DEVELOPMENTS IN PREPARATIVE, PROCESSING, AND EVALUATION METHODS: New Approaches to the Synthesis of Crystalline. Fiber-Forming Aliphatic Copolyesters. Advances in Morphological Development to Tailor the Performance of Me

  12. Lattice polymer automata

    Energy Technology Data Exchange (ETDEWEB)

    Rasmussen, S. [Los Alamos National Lab., NM (United States)]|[Santa Fe Institute, NM (United States); Smith, J.R. [Santa Fe Institute, NM (United States)]|[Massachusetts Media Lab., Cambridge, MA (United States). Physics and Media Group

    1995-05-01

    We present a new style of molecular dynamics and self-assembly simulation, the Lattice Polymer Automaton (LPA). In the LPA all interactions, including electromagnetic forces, are decomposed and communicated via propagating particles, {open_quotes}photons.{close_quotes} The monomer-monomer bondforces, the molecular excluded volume forces, the longer range intermolecular forces, and the polymer-solvent interactions may all be modeled with propagating particles. The LPA approach differs significantly from both of the standard approaches, Monte Carlo lattice methods and Molecular Dynamics simulations. On the one hand, the LPA provides more realism than Monte Carlo methods, because it produces a time series of configurations of a single molecule, rather than a set of causally unrelated samples from a distribution of configurations. The LPA can therefore be used directly to study dynamical properties; one can in fact watch polymers move in real time. On the other hand, the LPA is fully discrete, and therefore much simpler than traditional Molecular Dynamics models, which are continuous and operate on much shorter time scales. Due to this simplicity it is possible to simulate longer real time periods, which should enable the study of molecular self-organization on workstations supercomputers are not needed.

  13. Polymer crowding and shape distributions in polymer-nanoparticle mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Lim, Wei Kang; Denton, Alan R., E-mail: alan.denton@ndsu.edu [Department of Physics, North Dakota State University, Fargo, North Dakota 58108-6050 (United States)

    2014-09-21

    Macromolecular crowding can influence polymer shapes, which is important for understanding the thermodynamic stability of polymer solutions and the structure and function of biopolymers (proteins, RNA, DNA) under confinement. We explore the influence of nanoparticle crowding on polymer shapes via Monte Carlo simulations and free-volume theory of a coarse-grained model of polymer-nanoparticle mixtures. Exploiting the geometry of random walks, we model polymer coils as effective penetrable ellipsoids, whose shapes fluctuate according to the probability distributions of the eigenvalues of the gyration tensor. Accounting for the entropic cost of a nanoparticle penetrating a larger polymer coil, we compute the crowding-induced shift in the shape distributions, radius of gyration, and asphericity of ideal polymers in a theta solvent. With increased nanoparticle crowding, we find that polymers become more compact (smaller, more spherical), in agreement with predictions of free-volume theory. Our approach can be easily extended to nonideal polymers in good solvents and used to model conformations of biopolymers in crowded environments.

  14. Use of Triple Detection Size Exclusion Chromatography to Characterize Polymer Branching Structures%三检测体积排除色谱表征聚合物支化结构

    Institute of Scientific and Technical Information of China (English)

    刘云; 黄文艳; 田维新; 薛小强; 杨宏军; 蒋必彪

    2013-01-01

    以α-溴代异丁酸叔丁酯(t-BBiB)为引发剂,CuBr/联二吡啶为催化体系,二乙烯苯(DVB)为支化单体,采用原子转移自由基聚合反应(ATRP)经过一步加料方法和先臂后核方法分别合成不同支化结构类型的支化聚合物,同时以四官能度引发剂经ATRP合成臂数确定的星形聚合物为参照.采用三检测体积排除色谱(TD-SEC)得到Zimm相对支化因子g'与g和表征聚合物支化结构类型的指数因子ε(g'=gε).结果表明:随支化结构类型的不同,支化结构指数因子ε表现出不同的分子量依赖特性.星状支化聚合物的ε平均值<1,而且随分子量的变化保持相对恒定;无规支化聚合物的ε平均值>1,而且其值随分子量的增加不断减小.因此,可以由三检测体积排除色谱进行分析确证聚合物的支化结构类型.%The branched polymers with different branching structures were synthesized through atom transfer radical polymerization (ATRP) via controlling the adding method of divinylbenzene (DVB).The four-arm star polymers with different arm length were also prepared by ATRP as the reference for branching structure characterization.Triple detection size exclusion chromatography (TD-SEC) analysis showed that the exponential factor ε had a strong molecular weight dependence,here,ε (g'=gε) is the branching structure parameter expressed by Zimm branching factors g'= [Intrinsic Viscosity]branched/[Intrinsic Viscosity]linear and g = [Mean Square Radii of gyration]branched/[Mean Square Radii of gyration]linear at the same molecular weight.The average ε value of star-like branched polymers was less than unity,and remained relatively constant with the change of molecular weight; while the average ε value of randomly branched polymers was larger than unity,and decreased gradually with increased molecular weight.Therefore,the polymer branching structure can be characterized using TD-SEC.

  15. Processing polymers with cyclodextrins

    Science.gov (United States)

    Williamson, Brandon Robert

    Cyclodextrins (CDs) are cyclic starch molecules that have the unique ability to include a variety of small molecules and polymers inside their cavities, forming "Inclusion Complexes" (ICs). While much work has been done to understand the formation and behavior of these ICs, far less is known about the fundamental property changes that can occur when CD is used to alter polymer chain morphology. The goal of my graduate research has been to discover different ways to improve upon existing polymer properties through CD processing, as well as explore the possibility of creating a novel type of IC using non-traditional forms of cyclodextrin. Poly(ε-caprolactone) (PCL) was processed with alpha-CD to form an IC. The cyclodextrin was then stripped away to yield a PCL with elongated, unentangled, and constrained polymer chains, a process referred to as coalescence. The physical and rheological property changes resulting from this coalescence were then examined. It was found that reorganizing PCL in this manner resulted in an increase in the melt crystallization temperature of up to 25°C. Coalescence also decreased the tan delta of the material and increased the average hardness and Young's modulus by 33 and 53%, respectively. Non-stoichiometric ICs (NS-ICs), or ICs with at least parts of some polymer chains uncovered, were formed between poly (methyl methacrylate) (PMMA) and gamma-CD as well as a synthesized poly(ε-caprolactone)-poly(propylene glycol)-poly(ε-caprolactone) (PCL-PPG-PCL) triblock copolymer and beta-CD. The property changes of the non-complexed polymer chains were then studied. The PMMA/gamma-CD NS-IC samples were determined to be extremely heterogeneous, however glass transition temperature increases of up to 27°C above that of as-received PMMA were observed. Diffraction data for the PMMA NS-ICs suggests slight crystallinity at partial coverage, with a similar crystal structure to that of the fully covered IC. XRD, DSC and FTIR data revealed an almost

  16. Claisen thermally rearranged (CTR) polymers

    Science.gov (United States)

    Tena, Alberto; Rangou, Sofia; Shishatskiy, Sergey; Filiz, Volkan; Abetz, Volker

    2016-01-01

    Thermally rearranged (TR) polymers, which are considered the next-generation of membrane materials because of their excellent transport properties and high thermal and chemical stability, are proven to have significant drawbacks because of the high temperature required for the rearrangement and low degree of conversion during this process. We demonstrate that using a [3,3]-sigmatropic rearrangement, the temperature required for the rearrangement of a solid glassy polymer was reduced by 200°C. Conversions of functionalized polyimide to polybenzoxazole of more than 97% were achieved. These highly mechanically stable polymers were almost five times more permeable and had more than two times higher degrees of conversion than the reference polymer treated under the same conditions. Properties of these second-generation TR polymers provide the possibility of preparing efficient polymer membranes in a form of, for example, thin-film composite membranes for various gas and liquid membrane separation applications.

  17. Terminology of Polymers Containing Ionizable or Ionic Groups and of Polymers Containing Ions, VII.3

    Directory of Open Access Journals (Sweden)

    Jarm, V.

    2009-10-01

    Full Text Available The class of ionic polymers has widespread application in many areas of everyday life, in industrial production, and in the processes of living matter. The properties of ionic polymers depend on the polymer structure, and the nature, content, and location of the ionic groups. To clear differences among various ionic polymers, the IUPAC recommendations present 34 definitionsfor the ionomer, polyacid, polybase, polyampholytic polymer, ion-exchange polymer, polybetaine, polyelectrolyte, intrinsically conducting polymer, solid polymer electrolyte, etc

  18. Method for bonding a thermoplastic polymer to a thermosetting polymer component

    OpenAIRE

    Van Tooren, M.J.L.

    2012-01-01

    The invention relates to a method for bonding a thermoplastic polymer to a thermosetting polymer component, the thermoplastic polymer having a melting temperature that exceeds the curing temperature of the thermosetting polymer. The method comprises the steps of providing a cured thermosetting polymer component comprising an implant of a thermoplastic polymer at least at the part of the thermosetting polymer component to be bonded, locating a thermoplastic polymer in contact with at least the...

  19. Investigations of functional electroactive polymers

    OpenAIRE

    Tiitu, Mari

    2006-01-01

    Conjugated polymers containing pi-conjugated backbones form a scientifically and technologically important class of polymers. In their undoped form they are semiconductors, but they can be doped for electrical conductivity, and allow redox-activity, which all can lead to functional materials. One of the most important conjugated polymers in large scale applications is polyaniline due to its economics and good stability. Polyaniline is used for applications requiring conductivity as well as co...

  20. Functional polymer blends and nanocomposites

    OpenAIRE

    Weder, Christoph

    2010-01-01

    The broad class of (multi)functional polymers with unusual combinations of optical, electronic, mechanical and other properties is attracting significant interest, because it conceptually combines the advantages of polymers - low cost, ease of processing and a range of attractive mechanical characteristics - with the specific, tailorable properties of functional organic molecules. The caveat is that the synthesis of functional polymers is frequently complex and involves many steps, which make...

  1. Friction between Ring Polymer Brushes

    OpenAIRE

    2015-01-01

    Friction between ring-polymer brushes at melt densities sliding past each other are studied using extensive course-grained molecular dynamics simulations and scaling arguments, and the results are compared to the friction between linear-polymer brushes. We show that for a velocity range spanning over three decades, the frictional forces measured for ring-polymer brushes are half the corresponding friction in case of linear brushes. In the linear-force regime, the weak inter-digitation of two ...

  2. Wear of polymers and composites

    CERN Document Server

    Abdelbary, Ahmed

    2015-01-01

    In the field of tribology, the wear behaviour of polymers and composite materials is considered a highly non-linear phenomenon. Wear of Polymers and Composites introduces fundamentals of polymers and composites tribology. The book suggests a new approach to explore the effect of applied load and surface defects on the fatigue wear behaviour of polymers, using a new tribometer and thorough experiments. It discusses effects of surface cracks, under different static and cyclic loading parameters on wear, and presents an intelligent algorithm, in the form of a neural network, to map the relations

  3. Progress in polymer solar cell

    Institute of Scientific and Technical Information of China (English)

    LI LiGui; LU GuangHao; YANG XiaoNiu; ZHOU EnLe

    2007-01-01

    This review outlines current progresses in polymer solar cell. Compared to traditional silicon-based photovoltaic (PV) technology, the completely different principle of optoelectric response in the polymer cell results in a novel configuration of the device and more complicated photovoltaic generation process. The conception of bulk-heterojunction (BHJ) is introduced and its advantage in terms of morphology is addressed. The main aspects including the morphology of photoactive layer, which limit the efficiency and stability of polymer solar cell, are discussed in detail. The solutions to boosting up both the efficiency and stability (lifetime) of the polymer solar cell are highlighted at the end of this review.

  4. Polymer-based solar cells

    Directory of Open Access Journals (Sweden)

    Alex C. Mayer

    2007-11-01

    Full Text Available A significant fraction of the cost of solar panels comes from the photoactive materials and sophisticated, energy-intensive processing technologies. Recently, it has been shown that the inorganic components can be replaced by semiconducting polymers capable of achieving reasonably high power conversion efficiencies. These polymers are inexpensive to synthesize and can be solution-processed in a roll-to-roll fashion with high throughput. Inherently poor polymer properties, such as low exciton diffusion lengths and low mobilities, can be overcome by nanoscale morphology. We discuss polymer-based solar cells, paying particular attention to device design and potential improvements.

  5. Small angle scattering and polymers

    Energy Technology Data Exchange (ETDEWEB)

    Cotton, J.P. [Laboratoire Leon Brillouin (LLB) - Centre d`Etudes de Saclay, 91 - Gif-sur-Yvette (France)

    1996-12-31

    The determination of polymer structure is a problem of interest for both statistical physics and industrial applications. The average polymer structure is defined. Then, it is shown why small angle scattering, associated with isotopic substitution, is very well suited to the measurement of the chain conformation. The corresponding example is the old, but pedagogic, measurement of the chain form factor in the polymer melt. The powerful contrast variation method is illustrated by a recent determination of the concentration profile of a polymer interface. (author) 12 figs., 48 refs.

  6. ORGANOSILANE POLYMERS:OXIDATION-CROSSLINKABLE CYCLOTETRAMETHYLENESILYLENE POLYMER AND COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xinghua; Robert West

    1987-01-01

    Polysilane polymers containing cyclotetramethylenesilylene units were synthesized by sodium coupling of diorganodichlorosilanes in toluene. These polymers are soluble in common solvents, can be formed into a variety of shapes by molding, casting, coating or potting. They can be crosslinked by irradiation and oxidation at moderate or room temperature.

  7. Thermoresponsive Polymers for Nuclear Medicine: Which Polymer Is the Best?

    Science.gov (United States)

    Sedláček, Ondřej; Černoch, Peter; Kučka, Jan; Konefal, Rafał; Štěpánek, Petr; Vetrík, Miroslav; Lodge, Timothy P; Hrubý, Martin

    2016-06-21

    Thermoresponsive polymers showing cloud point temperatures (CPT) in aqueous solutions are very promising for the construction of various systems in biomedical field. In many of these applications these polymers get in contact with ionizing radiation, e.g., if they are used as carriers for radiopharmaceuticals or during radiation sterilization. Despite this fact, radiosensitivity of these polymers is largely overlooked to date. In this work, we describe the effect of electron beam ionizing radiation on the physicochemical and phase separation properties of selected thermoresponsive polymers with CPT between room and body temperature. Stability of the polymers to radiation (doses 0-20 kGy) in aqueous solutions increased in the order poly(N-vinylcaprolactam) (PVCL, the least stable) ≪ poly[N-(2,2-difluoroethyl)acrylamide] (DFP) polymer radiotherapeutics and sterilization of biomedical systems, cause significant increase in molecular weight due to cross-linking (except for POX, where this effect is weak). In the case of PVCL irradiated with low doses, the increase in molecular weight induced an increase in the CPT of the polymer. For PNIPAM and DFP, there is strong chain hydrophilization leading to an increase in CPT. From this perspective, POX is the most suitable polymer for the construction of delivery systems that experience exposure to radiation, while PVCL is the least suitable and PNIPAM and DFP are suitable only for low radiation demands.

  8. Thermoresponsive Polymers for Nuclear Medicine: Which Polymer Is the Best?

    Science.gov (United States)

    Sedláček, Ondřej; Černoch, Peter; Kučka, Jan; Konefal, Rafał; Štěpánek, Petr; Vetrík, Miroslav; Lodge, Timothy P; Hrubý, Martin

    2016-06-21

    Thermoresponsive polymers showing cloud point temperatures (CPT) in aqueous solutions are very promising for the construction of various systems in biomedical field. In many of these applications these polymers get in contact with ionizing radiation, e.g., if they are used as carriers for radiopharmaceuticals or during radiation sterilization. Despite this fact, radiosensitivity of these polymers is largely overlooked to date. In this work, we describe the effect of electron beam ionizing radiation on the physicochemical and phase separation properties of selected thermoresponsive polymers with CPT between room and body temperature. Stability of the polymers to radiation (doses 0-20 kGy) in aqueous solutions increased in the order poly(N-vinylcaprolactam) (PVCL, the least stable) ≪ poly[N-(2,2-difluoroethyl)acrylamide] (DFP) polymer radiotherapeutics and sterilization of biomedical systems, cause significant increase in molecular weight due to cross-linking (except for POX, where this effect is weak). In the case of PVCL irradiated with low doses, the increase in molecular weight induced an increase in the CPT of the polymer. For PNIPAM and DFP, there is strong chain hydrophilization leading to an increase in CPT. From this perspective, POX is the most suitable polymer for the construction of delivery systems that experience exposure to radiation, while PVCL is the least suitable and PNIPAM and DFP are suitable only for low radiation demands. PMID:27238593

  9. Radiation Synthesis of Superabsorbent Polymers Based on Natural Polymers

    International Nuclear Information System (INIS)

    The objectives of proposed research contract were first synthesize superabsorbent polymers based on natural polymers to be used as disposable diapers and soil conditioning materials in agriculture, horticulture and other super adsorbent using industries. We have planned to use the natural polymers; locust beam gum, tara gum, guar gum and sodium alginate on the preparation of natural superabsorbent polymers(SAP). The aqueous solution of natural polymers and their blends with trace amount of monomer and cross-linking agents will be irradiated in paste like conditions by gamma rays for the preparation of cross-linked superabsorbent systems. The water absorption and deswellling capacity of prepared super adsorbents and retention capacity, absorbency under load, suction power, swelling pressure and pet-rewet properties will be determined. Use of these materials instead of synthetic super absorbents will be examined by comparing the performance of finished products. The experimental studies achieved in the second year of project mainly on the effect of radiation on the chemistry of sodium alginate polymers in different irradiation conditions and structure-property relationship particularly with respect to radiation induced changes on the molecular weight of natural polymers and preliminary studies on the synthesis of natural-synthetic hydride super adsorbent polymers were given in details

  10. All Polymer Micropump

    DEFF Research Database (Denmark)

    Hansen, Thomas Steen

    2008-01-01

    of the substrate, the PEDOT is integrated into the non-conductive polymer. The result is a material that retains the good conductivity of PEDOT, but gains the mechanical stability of the substrate. The best results were obtained for PEDOTjPMMA. The new mechanically stable PEDOTjPMMA was micro-patterned using clean...... (ACEO) micropump. The ACEO pump consists of an array of interdigitated small and large PEDOTjPMMA encapsulated in a polyurethane (PUR) channel system. The pumping velocity was detected using fluorescent microspheres and a confocal microscope. The pump characteristics resembled those of pumps based...

  11. Controlled Synthesis of Polymer Brushes via Polymer Single Crystal Templates

    Science.gov (United States)

    Zhou, Tian

    A novel synthetic method of polymer brushes using polymer single crystals (PSCs) as solid-state templates is introduced in this study. PSC has a quasi-2D lamellae structure with polymer chains fold back-and-forth perpendicular to the lamellae surfaces. During crystallization, the chain ends are excluded from the unit cell onto the lamellae surfaces, which makes the material extremely versatile in its functionality. Such structure holds the unique capability to harvest nanoparticles, or being immobilized onto macroscopic flat surfaces. After dissolving PSCs in good solvent, polymer brushes are chemically tethered on either nanoparticles or flat macroscopic surfaces. Because the chain-folding structure can be conveniently tailored by changing the molecular weight of polymer and the crystallization temperature, the thickness, grafting density and morphology of resulted polymer brushes can be precisely controlled. As a model system, poly(?-caprolactone) with thiol or alkoxysilane terminal groups was used, and polymer brushes were successfully prepared on both nanoparticles and glass/Au flat surfaces. The structure-property relationships of the as-prepared polymer brushes were studied in detail using multiple characterization techniques. First of all, when functionalizing nanoparticles, by engineering the chain-folding structure of the PSCs, interesting complex nanostructures can be formed by nanoparticles including Janus nanoparticles and nanoparticle dimers. These unique structures render hybrid nanoparticles very interesting responsive behavior which have been studied in detail in this dissertation. When grafted onto a flat surface on the other hand, not only the molecular weight and grafting density can be precisely controlled, the tethering points of a single polymer chain can also be conveniently tailored, resulting polymer brushes with either tail or loop structures. Such difference in brush structure can significantly alter the properties of functional surface

  12. Development of Bionic Polymers

    Institute of Scientific and Technical Information of China (English)

    Xu Jian; Xie Qiongdan; Guo Xinlin; Feng Lin; Jiang Lei; Tang Wenghong; Luo Xiandong; Zhang Xiaoli; Han Charles C.

    2004-01-01

    Bionics, an artificial imitation of natural products, has always been a forever dream in the fairy tale or scientific fiction when we were childhood and children live now. However, the development of science in molecular scale makes this dream of childhood and manhood realize today.Bionics, a branch of science concerned with application the data about the functioning of biological system to the solution of engineering problems, become top-priority of science in the 21st century.However, few examples are given in molecular-level or nano-scale controlling lotus-like surface (a bionic surface for vast potential application). In the same time, such a typical bionic surface (as well known, so called "Lotus-effect") is a symbol or a totem that scientists can develop a novel approach to prepare desired surface and to control its microstructure or morphology at one's pleasure.In general, a film with a water contact angle (CA) higher than 150° can be defined as a superhydrophobic surface. The Langmuir-Blodgett film prepared by using CF3(CF2)10COOH possesses the lowest surface tension, which is 6 mJ/m2 (1). However, the water CA on a smooth surface with regularly aligned C20F42 with close-hexagonal packed -CF3 groups is only 119° (2).Obviously, only adjusting chemical composition is not enough to produce a superhydrophobic surface. Wenzel et al (3) suggested that the contact angle θ' of a liquid droplet on a rough solid surface should be written as:cosθ, =γcosθ = γ(γs-γsl)/γl, here γ is a roughness factor and γsl, γs and γl denote the interfacial tensions of the solid-liquid, the solid-gas, and the liquid-gas interfaces,respectively. This γ is always larger than 1 and a rough surface will be more water-repellent or more wettable to a liquid when intrinsic contact angle θ is bigger or smaller than 90°, respectively.Therefore, a general approach to obtain superhydrophobic surfaces is using a combination of depressing surface energy and enhancing surface

  13. Thermal conductivity and multiferroics of electroactive polymers and polymer composites

    Science.gov (United States)

    Jin, Jiezhu

    Electronically conducting polymers and electromechanical polymers are the two important branches of the cutting-edge electroactive polymers. They have shown significant impact on many modern technologies such as flat panel display, energy transport, energy conversion, sensors and actuators. To utilize conducting polymers in microelectronics, optoelectronics and thermoelectrics, it is necessary to have a comprehensive study of their thermal conductivity since thermal conductivity is a fundamental materials property that is particularly important and sometimes a determining factor of the device performance. For electromechanical polymers, larger piezoelectric effect will contribute to the improvement of magnetoelectric (ME) coupling efficiency in their multiferroic composites. This dissertation is devoted to characterizing electronically conducting polymers for their electrical and thermal conductivity, and developing new classes of electromechanical polymers and strain-mediated electromechanical polymer-based multiferroic ME composites. Conducting polymers opened up new possibilities for devices combining novel electrical and thermal properties, but there has been limited understanding of the length-scale effect of the electrical and thermal conductivity, and the mechanism underlying the electricity and heat transport behavior. In this dissertation, the analytical model and experimental technique are presented to measure the in-plane thermal conductivity of polyaniline thin films. For camphorsulfonic acid doped polyaniline patterned on silicon oxide/silicon substrate using photolithography and reactive ion etching, the thermal conductivity of the film with thickness of 20 nm is measured to be 0.0406 W/m˙K, which significantly deviates from their bulk (> 0.26 W/m˙K). The size effect on thermal conductivity at this scale is attributed to the significant phonon boundary scattering. When the film goes up to 130 nm thick, the thermal conductivity increases to 0.166 W

  14. Graphene/Polymer Nanocomposites

    Science.gov (United States)

    Macosko, Chris

    2010-03-01

    Graphite has attracted large attention as a reinforcement for polymers due to its ability to modify electrical conductivity, mechanical and gas barrier properties of host polymers and its potentially lower cost than carbon nanotubes. If graphite can be exfoliated into atomically thin graphene sheets, it is possible to achieve the highest property enhancements at the lowest loading. However, small spacing and strong van der Waals forces between graphene layers make exfoliation of graphite via conventional composite manufacturing strategies challenging. Recently, two different approaches to obtain exfoliated graphite prior to blending were reported: thermal treatment (Schniepp et al., JACS 2006) and chemical modification (Stankovich et al., J Mat Chem 2006). Both start from graphite oxide. We will describe and evaluate these exfoliation approaches and the methods used to produce graphene reinforced thermoplastics, particularly polyester, polycarbonate and polyurethane nanocomposites. Three different dispersion methods - melt blending, solution mixing and in-situ polymerization -- are compared. Characterization of dispersion quality is illustrated with TEM, rheology and in electrical conductivity, tensile modulus and gas barrier property improvement.

  15. Polymer dye lasers

    DEFF Research Database (Denmark)

    Balslev, Søren

    2006-01-01

    , elektronstrålelithografi og Röntgenstrålelithografi. Andre polymerer er også blevet formgivet via ”nanoimprint” lithografi for at skabe laserresonatorer. En række lasere, både baseret på et flydende forstærkningsmedium og et faststof forstærkningsrmedium er blevet udviklet. Laserne giver både lys i flere ”modes” og i een......Formålet med dette Ph.D. arbejde har været at udvikle miniaturiserede polymer farvestoflasere, egnet til at blive integreret i mikrochips som også indeholder andre polymerstrukturer – som for eksempel kan findes i ”Laboratorie-på-en-chip” kredsløb. Lasernes funktion skal være at levere lys til...... meget følsomme sensorformål, og at undgå at skulle opliniere eksterne lyskilder til sensorer på polymerchips. En enkelt type gennemsigtig ”resist” (SU-8) er blevet brugt til at udvikle en række laserresonatorer i polymer. ”Resisten” er blevet formgivet via en række lithografiske teknikker: UV lithografi...

  16. Polymer-based photonic crystals

    Energy Technology Data Exchange (ETDEWEB)

    Edrington, A.C.; Urbas, A.M.; Fink, Y.; Thomas, E.L. [Massachusetts Inst. of Tech., Cambridge (United States). Dept. of Materials Science and Engineering; DeRege, P. [Firmenich, Inc., Port Newark, NJ (United States); Chen, C.X.; Swager, T.M. [Massachusetts Inst. of Tech., Cambridge, MA (United States). Dept. of Chemistry; Hadjichristidis, N. [Athens Univ. (Greece). Dept. of Chemistry; Xenidou, M.; Fetters, L.J. [ExxonMobil Research Corp., Annandale, NJ (United States); Joannopoulos, J.D. [Massachusetts Inst. of Tech., Cambridge, MA (United States). Dept. of Physics

    2001-03-16

    The development of polymers as photonic crystals is highlighted, placing special emphasis on self-assembled block copolymers. 1D self-assembled multilayers as well as 2D and 3D self-assembled structures are examined, then intricate block polymer structures such as that shown in the Figure are discussed as are birefringent multilayer and elastomeric films. (orig.)

  17. Wood and concrete polymer composites

    International Nuclear Information System (INIS)

    There are several ways to prepare and use wood and concrete polymer composites. The most important improvements in the case of concrete polymer composites are obtained for compressive and tensile strengths. The progress in this field in United States and other countries is discussed in this rview. (M.S.)

  18. Polymer highlights for September 1975

    Energy Technology Data Exchange (ETDEWEB)

    Hammon, H.G.; Althouse, L.P.; Buckner, A.T.; McKinley, B.; Walkup, C.M.; Rinde, J.; Lorensen, L.L.; Cady, W.E.; Caley, L.E.

    1988-12-15

    Research programs in polymer chemistry are briefly described. The following polymers are under investigation for use as adhesives, nozzles, insulators, or fluid cushions: urethanes, teflon, TFE, Tefzel, Ryton, H Resin, Imidite 2803, PPQ, KELF 800, and KELF 5500. Areas of research application include geothermal and solar energy fields. (CBS)

  19. POLYMERS BEYOND THE YEAR 2000

    Institute of Scientific and Technical Information of China (English)

    Ingolf Buethe

    2000-01-01

    At the turn of the century, the global polymer industry is undergoing the most rapid and dramatic changes in its history. Emerging markets, particularly in Asia, and their polymer consumption are catching up with other parts of the world,creating new business opportunities. Economy of scale, combined with optimized logistic concepts, is becoming a key economic success factor, thus forcing smaller suppliers out of business and creating a major hurdle for newcomers and the introduction of new products. Globalization of polymer customers and cost pressure lead to a consolidation of suppliers and products. Today standard thermoplastics have a dominant position in the market and they will retain this position in future.Engineering thermoplastics are facing growing competition due to the increased efficiency of standard polymers. This leads to a displacement process where standard polymers substitute engineering thermoplastics. Simultaneously engineering polymers are pushing into new markets or applications or displacing materials like glass, wood or metal. The recent history and future trends have a strong impact on R&D activity in the polymer industry. Competition on a global scale and increasing cost pressure are turning innovation into an essential precondition of commercial success, thus determining the objectives of industrial polymer research and development.

  20. All-Polymer Electrochemical Sensors

    DEFF Research Database (Denmark)

    Kafka, Jan Robert

    This thesis presents fabrication strategies to produce different types of all-polymer electrochemical sensors based on electrodes made of the highly conductive polymer poly(3,4-ethylenedioxythiophene) (PEDOT). Three different systems are presented, fabricated either by using microdrilling or by hot...

  1. Fifty years of polymer science

    NARCIS (Netherlands)

    Prez, Du Filip; Hoogenboom, Richard; Klumperman, Bert; Meier, Michael; Monteiro, Michael; Müller, Alejandro; Vancso, Julius

    2015-01-01

    The European Polymer Journal (EPJ) has been serving the scientific community for 50 years, which makes it one of the older macromolecular journals with a broad focus. Since its launch 50 years ago, EPJ has provided a distinguished forum for publications in polymer research, including chemistry, phys

  2. Review of polymer MEMS micromachining

    Science.gov (United States)

    Kim, Brian J.; Meng, Ellis

    2016-01-01

    The development of polymer micromachining technologies that complement traditional silicon approaches has enabled the broadening of microelectromechanical systems (MEMS) applications. Polymeric materials feature a diverse set of properties not present in traditional microfabrication materials. The investigation and development of these materials have opened the door to alternative and potentially more cost effective manufacturing options to produce highly flexible structures and substrates with tailorable bulk and surface properties. As a broad review of the progress of polymers within MEMS, major and recent developments in polymer micromachining are presented here, including deposition, removal, and release techniques for three widely used MEMS polymer materials, namely SU-8, polyimide, and Parylene C. The application of these techniques to create devices having flexible substrates and novel polymer structural elements for biomedical MEMS (bioMEMS) is also reviewed.

  3. Neutron scattering in polymer physics

    Science.gov (United States)

    Richter, D.

    2000-03-01

    By example this short review presents recent scientific advances which were achieved by the application of neutron scattering to polymer systems, thereby, keeping in mind also practical applications. We first focus on experiments on the structure and morphology of polymer systems covering conformational studies, investigations on polymer-microemulsions systems and the observation of aggregation states in living polymerization. Thereafter, we present recent results in the field of polymer dynamics. We begin with local motions which are behind the classical relaxation processes in polymer melts. Then we relate to universal dynamics, we address the Rouse model and its limits, present new results on the dynamic miscibility in blends and display the latest investigations on entanglement dynamics. Finally, we report first observations of ripplon excitations of phase boundaries in diblock copolymer melts.

  4. Controlled release from recombinant polymers.

    Science.gov (United States)

    Price, Robert; Poursaid, Azadeh; Ghandehari, Hamidreza

    2014-09-28

    Recombinant polymers provide a high degree of molecular definition for correlating structure with function in controlled release. The wide array of amino acids available as building blocks for these materials lend many advantages including biorecognition, biodegradability, potential biocompatibility, and control over mechanical properties among other attributes. Genetic engineering and DNA manipulation techniques enable the optimization of structure for precise control over spatial and temporal release. Unlike the majority of chemical synthetic strategies used, recombinant DNA technology has allowed for the production of monodisperse polymers with specifically defined sequences. Several classes of recombinant polymers have been used for controlled drug delivery. These include, but are not limited to, elastin-like, silk-like, and silk-elastinlike proteins, as well as emerging cationic polymers for gene delivery. In this article, progress and prospects of recombinant polymers used in controlled release will be reviewed.

  5. Polymer research by neutron scattering

    International Nuclear Information System (INIS)

    Polymer physics aims on an understanding of the macroscopic behavior of polymer systems on the basis of their molecular structure and dynamics. For this purpose neutrons serve as a unique probe, allowing a simultaneous investigation of polymer structure and dynamics on a molecular scale. Furthermore, hydrogen deuterium exchange facilitates molecular labeling and offers the possibility to observe selected chains or chain parts in dense systems. Neutron small angle scattering reveals information on the conformation and possible aggregation of polymer chains. Data on linear and star like molecules are shown as examples. High resolution neutron spin-echospectroscopy observes the molecular dynamics of long chain molecules. Results on the large scale motion of chins in polymer melts are presented. finally, experiments on chain relaxation close to the glass transition are displayed. Three distinctly different relaxation processes are revealed. (author)

  6. Polymers for Cardiovascular Stent Coatings

    Directory of Open Access Journals (Sweden)

    Anne Strohbach

    2015-01-01

    Full Text Available Polymers have found widespread applications in cardiology, in particular in coronary vascular intervention as stent platforms (scaffolds and coating matrices for drug-eluting stents. Apart from permanent polymers, current research is focussing on biodegradable polymers. Since they degrade once their function is fulfilled, their use might contribute to the reduction of adverse events like in-stent restenosis, late stent-thrombosis, and hypersensitivity reactions. After reviewing current literature concerning polymers used for cardiovascular applications, this review deals with parameters of tissue and blood cell functions which should be considered to evaluate biocompatibility of stent polymers in order to enhance physiological appropriate properties. The properties of the substrate on which vascular cells are placed can have a large impact on cell morphology, differentiation, motility, and fate. Finally, methods to assess these parameters under physiological conditions will be summarized.

  7. Color formation in irradiated polymers

    Science.gov (United States)

    Clough, R. L.; Gillen, K. T.; Malone, G. M.; Wallace, J. S.

    1996-11-01

    Discoloration is a problem in the radiation processing of polymers (such as radiation sterilization), and also in emerging applications in which optical-property materials are used in radiation environments (such as scintillation detectors). We have completed a survey of 17 different types of optical polymers, in which it is found that these materials form both permanent and annealable color centers, but in very different magnitudes and ratios. Optical absorption spectra of irradiated polymers both immediately after irradiation and following different time periods of annealing are provided. Also provided are tables showing rank ordering of the relative resistance of different polymer types to induced discoloration. It is found that the extent of radiation-induced discoloration of polymers has little or no dependence on whether the macromolecule is aromatic or aliphatic, and shows no correlation with the relative extent of radiation-induced mechanical property change. Examples of the influence of stabilizer additives on the extent of discoloration are discussed.

  8. Direct Photopatterning of Electrochromic Polymers

    DEFF Research Database (Denmark)

    Jensen, Jacob; Dyer, Aubrey L.; Shen, D. Eric;

    2013-01-01

    Propylenedioxythiophene (ProDOT) polymers are synthesized using an oxidative polymerization route that results in methacrylate substituted poly(ProDOTs) having a Mn of 10–20 kDa wherein the methacrylate functionality constitutes from 6 to 60% of the total monomer units. Solutions of these polymers...... show excellent film forming abilities, with thin films prepared using both spray‐casting and spin‐coating. These polymers are demonstrated to crosslink upon UV irradiation at 350 nm, in the presence of an appropriate photoinitiator, to render the films insoluble to common organic solvents....... Electrochemical, spectroelectrochemical, and colorimetric analyses of the crosslinked polymer films are performed to establish that they retain the same electrochromic qualities as the parent polymers with no detriment to the observed properties. To demonstrate applicability for multi‐film processing...

  9. Fundamental studies of polymer filtration

    Energy Technology Data Exchange (ETDEWEB)

    Smith, B.F.; Lu, M.T.; Robison, T.W.; Rogers, Y.C.; Wilson, K.V.

    1998-12-31

    This is the final report of a one-year, Laboratory Directed Research and Development (LDRD) project at Los Alamos National Laboratory (LANL). The objectives of this project were (1) to develop an enhanced fundamental understanding of the coordination chemistry of hazardous-metal-ion complexation with water-soluble metal-binding polymers, and (2) to exploit this knowledge to develop improved separations for analytical methods, metals processing, and waste treatment. We investigated features of water-soluble metal-binding polymers that affect their binding constants and selectivity for selected transition metal ions. We evaluated backbone polymers using light scattering and ultrafiltration techniques to determine the effect of pH and ionic strength on the molecular volume of the polymers. The backbone polymers were incrementally functionalized with a metal-binding ligand. A procedure and analytical method to determine the absolute level of functionalization was developed and the results correlated with the elemental analysis, viscosity, and molecular size.

  10. Grafted polymer under shear flow

    Science.gov (United States)

    Kumar, Sanjiv; Foster, Damien P.; Giri, Debaprasad; Kumar, Sanjay

    2016-04-01

    A self-attracting-self-avoiding walk model of polymer chain on a square lattice has been used to gain an insight into the behaviour of a polymer chain under shear flow in a slit of width L. Using exact enumeration technique, we show that at high temperature, the polymer acquires the extended state continuously increasing with shear stress. However, at low temperature the polymer exhibits two transitions: a transition from the coiled to the globule state and a transition to a stem-flower like state. For a chain of finite length, we obtained the exact monomer density distributions across the layers at different temperatures. The change in density profile with shear stress suggests that the polymer under shear flow can be used as a molecular gate with potential application as a sensor.

  11. Review of polymer MEMS micromachining

    International Nuclear Information System (INIS)

    The development of polymer micromachining technologies that complement traditional silicon approaches has enabled the broadening of microelectromechanical systems (MEMS) applications. Polymeric materials feature a diverse set of properties not present in traditional microfabrication materials. The investigation and development of these materials have opened the door to alternative and potentially more cost effective manufacturing options to produce highly flexible structures and substrates with tailorable bulk and surface properties. As a broad review of the progress of polymers within MEMS, major and recent developments in polymer micromachining are presented here, including deposition, removal, and release techniques for three widely used MEMS polymer materials, namely SU-8, polyimide, and Parylene C. The application of these techniques to create devices having flexible substrates and novel polymer structural elements for biomedical MEMS (bioMEMS) is also reviewed. (topical review)

  12. Accelerated Characterization of Polymer Properties

    Energy Technology Data Exchange (ETDEWEB)

    R. Wroczynski; l. Brewer; D. Buckley; M. Burrell; R. Potyrailo

    2003-07-30

    This report describes the efforts to develop a suite of microanalysis techniques that can rapidly measure a variety of polymer properties of industrial importance, including thermal, photo-oxidative, and color stability; as well as ductility, viscosity, and mechanical and antistatic properties. Additional goals of the project were to direct the development of these techniques toward simultaneous measurements of multiple polymer samples of small size in real time using non-destructive and/or parallel or rapid sequential measurements, to develop microcompounding techniques for preparing polymers with additives, and to demonstrate that samples prepared in the microcompounder could be analyzed directly or used in rapid off-line measurements. These enabling technologies are the crucial precursors to the development of high-throughput screening (HTS) methodologies for the polymer additives industry whereby the rate of development of new additives and polymer formulations can be greatly accelerated.

  13. Polymer in Agriculture: a Review

    Directory of Open Access Journals (Sweden)

    Francesco Puoci

    2008-01-01

    Full Text Available In agricultural field, polymers are widely used for many applications. Although they were used, in the first time, just as structural materials (inhert polymers, in the last decades functionalized polymers revolutionized the agricultural and food industry with new tools for several applications. Smart polymeric materials and smart delivery systems helped the agricultural industryto combat viruses and other crop pathogens, functionalized polymers were used to increase the efficiency of pesticides and herbicides, allowing lower doses to be used and to indirectly protect the environment through filters or catalysts to reduce pollution and clean-up existing pollutants. This report will review the key aspects of used polymers in agricultural area, highlighting current research in this field and the future impacts they may have.

  14. Application to the radiation processing of polymer

    Energy Technology Data Exchange (ETDEWEB)

    Yoshii, Fumio [Japan Atomic Energy Research Inst., Takasaki, Gunma (Japan). Takasaki Radiation Chemistry Research Establishment

    2003-02-01

    Polypropylene (PP) and biodegradable polymer (blend of poly ({epsilon}-caploracton) 30/polybutylenesuccynate 70), PHB02 were irradiated with an electron beam to improve processability for production of thin film and foam. The processability of the polymer was improved due to enhancement of melt strength with irradiation at the dose range between 10 and 100 kGy. Increase of melt strength is due to entanglement of branch structure formed by irradiation. Possibility of high-speed production of thin film and production of foam have been achieved by this process. The soil degradation test showed that biodegradable polymer film buried in the soil was almost entirely degraded (97%) after two months and completely degraded after two and a half months. In the case of foam samples, 65% degradation was achieved after four months. Radiation crosslinked water-soluble polymer form hydrogel, which absorb much water. The hydrogel prepared by irradiation of polymer in aqueous solution was applied as dressing for healing of wound. In order to evaluate the healing effect of the polyethylene oxide (PEO) hydrogel dressing, wounds formed on the back of marmots were covered by the hydrogel. The healing under the wet environment of the hydrogel dressing had three advantages, compared with that of gauze dressing, which gives a dry environment: (1) enhancement of healing rate, (2) facilitation for changing the dressing, i.e. the hydrogel can be peeled off without any damage to the regenerated skin surface, and (3) hydrogel dressing material does not remain stuck on the wound. (author)

  15. Application to the radiation processing of polymer

    International Nuclear Information System (INIS)

    Polypropylene (PP) and biodegradable polymer (blend of poly (ε-caploracton) 30/polybutylenesuccynate 70), PHB02 were irradiated with an electron beam to improve processability for production of thin film and foam. The processability of the polymer was improved due to enhancement of melt strength with irradiation at the dose range between 10 and 100 kGy. Increase of melt strength is due to entanglement of branch structure formed by irradiation. Possibility of high-speed production of thin film and production of foam have been achieved by this process. The soil degradation test showed that biodegradable polymer film buried in the soil was almost entirely degraded (97%) after two months and completely degraded after two and a half months. In the case of foam samples, 65% degradation was achieved after four months. Radiation crosslinked water-soluble polymer form hydrogel, which absorb much water. The hydrogel prepared by irradiation of polymer in aqueous solution was applied as dressing for healing of wound. In order to evaluate the healing effect of the polyethylene oxide (PEO) hydrogel dressing, wounds formed on the back of marmots were covered by the hydrogel. The healing under the wet environment of the hydrogel dressing had three advantages, compared with that of gauze dressing, which gives a dry environment: (1) enhancement of healing rate, (2) facilitation for changing the dressing, i.e. the hydrogel can be peeled off without any damage to the regenerated skin surface, and (3) hydrogel dressing material does not remain stuck on the wound. (author)

  16. EDITORIAL: Electroactive polymer materials

    Science.gov (United States)

    Bar-Cohen, Yoseph; Kim, Kwang J.; Ryeol Choi, Hyouk; Madden, John D. W.

    2007-04-01

    Imitating nature's mechanisms offers enormous potential for the improvement of our lives and the tools we use. This field of the study and imitation of, and inspiration from, nature's methods, designs and processes is known as biomimetics. Artificial muscles, i.e. electroactive polymers (EAPs), are one of the emerging technologies enabling biomimetics. Polymers that can be stimulated to change shape or size have been known for many years. The activation mechanisms of such polymers include electrical, chemical, pneumatic, optical and magnetic. Electrical excitation is one of the most attractive stimulators able to produce elastic deformation in polymers. The convenience and practicality of electrical stimulation and the continual improvement in capabilities make EAP materials some of the most attractive among activatable polymers (Bar-Cohen Y (ed) 2004 Electroactive Polymer (EAP) Actuators as Artificial Muscles—Reality, Potential and Challenges 2nd edn, vol PM136 (Bellingham, WA: SPIE Press) pp 1-765). As polymers, EAP materials offer many appealing characteristics that include low weight, fracture tolerance and pliability. Furthermore, they can be configured into almost any conceivable shape and their properties can be tailored to suit a broad range of requirements. These capabilities and the significant change of shape or size under electrical stimulation while being able to endure many cycles of actuation are inspiring many potential possibilities for EAP materials among engineers and scientists in many different disciplines. Practitioners in biomimetics are particularly excited about these materials since they can be used to mimic the movements of animals and insects. Potentially, mechanisms actuated by EAPs will enable engineers to create devices previously imaginable only in science fiction. For many years EAP materials received relatively little attention due to their poor actuation capability and the small number of available materials. In the last fifteen

  17. Polymers – A New Open Access Scientific Journal on Polymer Science

    Directory of Open Access Journals (Sweden)

    Shu-Kun Lin

    2009-12-01

    Full Text Available Polymers is a new interdisciplinary, Open Access scientific journal on polymer science, published by Molecular Diversity Preservation International (MDPI. This journal welcomes manuscript submissions on polymer chemistry, macromolecular chemistry, polymer physics, polymer characterization and all related topics. Both synthetic polymers and natural polymers, including biopolymers, are considered. Manuscripts will be thoroughly peer-reviewed in a timely fashion, and papers will be published, if accepted, within 6 to 8 weeks after submission. [...

  18. SULFUR POLYMER ENCAPSULATION

    International Nuclear Information System (INIS)

    Sulfur polymer cement (SPC) is a thermoplastic polymer consisting of 95 wt% elemental sulfur and 5 wt% organic modifiers to enhance long-term durability. SPC was originally developed by the U.S. Bureau of Mines as an alternative to hydraulic cement for construction applications. Previous attempts to use elemental sulfur as a construction material in the chemical industry failed due to premature degradation. These failures were caused by the internal stresses that result from changes in crystalline structure upon cooling of the material. By reacting elemental sulfur with organic polymers, the Bureau of Mines developed a product that successfully suppresses the solid phase transition and significantly improves the stability of the product. SPC, originally named modified sulfur cement, is produced from readily available, inexpensive waste sulfur derived from desulfurization of both flue gases and petroleum. The commercial production of SPC is licensed in the United States by Martin Resources (Odessa, Texas) and is marketed under the trade name Chement 2000. It is sold in granular form and is relatively inexpensive ((approx)$0.10 to 0.12/lb). Application of SPC for the treatment of radioactive, hazardous, and mixed wastes was initially developed and patented by Brookhaven National Laboratory (BNL) in the mid-1980s (Kalb and Colombo, 1985; Colombo et al., 1997). The process was subsequently investigated by the Commission of the European Communities (Van Dalen and Rijpkema, 1989), Idaho National Engineering Laboratory (Darnell, 1991), and Oak Ridge National Laboratory (Mattus and Mattus, 1994). SPC has been used primarily in microencapsulation applications but can also be used for macroencapsulation of waste. SPC microencapsulation has been demonstrated to be an effective treatment for a wide variety of wastes, including incinerator hearth and fly ash; aqueous concentrates such as sulfates, borates, and chlorides; blowdown solutions; soils; and sludges. It is not

  19. Production of Cellulosic Polymers from Agricultural Wastes

    OpenAIRE

    Israel, A. U.; I. B. Obot; Umoren, S. A.; Mkpenie, V.; Asuquo, J. E.

    2008-01-01

    Cellulosic polymers namely cellulose, di-and triacetate were produced from fourteen agricultural wastes; Branch and fiber after oil extraction from oil palm (Elais guineensis), raffia, piassava, bamboo pulp, bamboo bark from raphia palm (Raphia hookeri), stem and cob of maize plant (Zea mays), fruit fiber from coconut fruit (Cocos nucifera), sawdusts from cotton tree (Cossypium hirsutum), pear wood (Manilkara obovata), stem of Southern gamba green (Andropogon tectorus), sugarcane baggase (Sac...

  20. Conducting Polymer Based Nanobiosensors

    Directory of Open Access Journals (Sweden)

    Chul Soon Park

    2016-06-01

    Full Text Available In recent years, conducting polymer (CP nanomaterials have been used in a variety of fields, such as in energy, environmental, and biomedical applications, owing to their outstanding chemical and physical properties compared to conventional metal materials. In particular, nanobiosensors based on CP nanomaterials exhibit excellent performance sensing target molecules. The performance of CP nanobiosensors varies based on their size, shape, conductivity, and morphology, among other characteristics. Therefore, in this review, we provide an overview of the techniques commonly used to fabricate novel CP nanomaterials and their biosensor applications, including aptasensors, field-effect transistor (FET biosensors, human sense mimicking biosensors, and immunoassays. We also discuss prospects for state-of-the-art nanobiosensors using CP nanomaterials by focusing on strategies to overcome the current limitations.

  1. Self-healing polymers

    Science.gov (United States)

    Klein, Daniel J. (Inventor)

    2011-01-01

    A three dimensional structure fabricated from a self-healing polymeric material, comprising poly(ester amides) obtained from ethylene glycol, azelaic acid and 1,1-aminoundecanoic acid, wherein polymeric material has a melt index above 2.5 g/10 min. as determined by ASTM D1238 at 190.degree. C. and 2.16kg, impact resistance and ductility sufficient to resist cracking and brittle fracture upon impact by a 9 mm bullet fired at a temperature of about 29.degree. C. at subsonic speed in a range from about 800 feet/sec to about 1000 feet/sec. It has been determined that the important factors necessary for self-healing behavior of polymers include sufficient impact strength, control of the degree of crystallinity, low melting point and the ability to instantly melt at impacted area.

  2. Polymers in Curved Boxes

    CERN Document Server

    Yaman, K; Solis, F J; Witten, T A

    1996-01-01

    We apply results derived in other contexts for the spectrum of the Laplace operator in curved geometries to the study of an ideal polymer chain confined to a spherical annulus in arbitrary space dimension D and conclude that the free energy compared to its value for an uncurved box of the same thickness and volume, is lower when $D < 3$, stays the same when $D = 3$, and is higher when lowers the effective bending elasticity of the walls, and might induce spontaneous symmetry breaking, i.e. bending. (Actually, the above mentioned results show that {\\em {any}} shell in $D = 3$ induces this effect, except for a spherical shell). We compute the contribution of this effect to the bending rigidities in the Helfrich free energy expression.

  3. Polymer Parametrised Field Theory

    CERN Document Server

    Laddha, Alok

    2008-01-01

    Free scalar field theory on 2 dimensional flat spacetime, cast in diffeomorphism invariant guise by treating the inertial coordinates of the spacetime as dynamical variables, is quantized using LQG type `polymer' representations for the matter field and the inertial variables. The quantum constraints are solved via group averaging techniques and, analogous to the case of spatial geometry in LQG, the smooth (flat) spacetime geometry is replaced by a discrete quantum structure. An overcomplete set of Dirac observables, consisting of (a) (exponentials of) the standard free scalar field creation- annihilation modes and (b) canonical transformations corresponding to conformal isometries, are represented as operators on the physical Hilbert space. None of these constructions suffer from any of the `triangulation' dependent choices which arise in treatments of LQG. In contrast to the standard Fock quantization, the non- Fock nature of the representation ensures that the algebra of conformal isometries as well as tha...

  4. Fragmentation pathways of polymer ions.

    Science.gov (United States)

    Wesdemiotis, Chrys; Solak, Nilüfer; Polce, Michael J; Dabney, David E; Chaicharoen, Kittisak; Katzenmeyer, Bryan C

    2011-01-01

    Tandem mass spectrometry (MS/MS) is increasingly applied to synthetic polymers to characterize chain-end or in-chain substituents, distinguish isobaric and isomeric species, and determine macromolecular connectivities and architectures. For confident structural assignments, the fragmentation mechanisms of polymer ions must be understood, as they provide guidelines on how to deduce the desired information from the fragments observed in MS/MS spectra. This article reviews the fragmentation pathways of synthetic polymer ions that have been energized to decompose via collisionally activated dissociation (CAD), the most widely used activation method in polymer analysis. The compounds discussed encompass polystyrenes, poly(2-vinyl pyridine), polyacrylates, poly(vinyl acetate), aliphatic polyester copolymers, polyethers, and poly(dimethylsiloxane). For a number of these polymers, several substitution patterns and architectures are considered, and questions regarding the ionization agent and internal energy of the dissociating precursor ions are also addressed. Competing and consecutive dissociations are evaluated in terms of the structural insight they provide about the macromolecular structure. The fragmentation pathways of the diverse array of polymer ions examined fall into three categories, viz. (1) charge-directed fragmentations, (2) charge-remote rearrangements, and (3) charge-remote fragmentations via radical intermediates. Charge-remote processes predominate. Depending on the ionizing agent and the functional groups in the polymer, the incipient fragments arising by pathways (1)-(3) may form ion-molecule complexes that survive long enough to permit inter-fragment hydrogen atom, proton, or hydride transfers. PMID:20623599

  5. Nanoscale Study of Polymer Dynamics.

    Science.gov (United States)

    Keshavarz, Masoumeh; Engelkamp, Hans; Xu, Jialiang; Braeken, Els; Otten, Matthijs B J; Uji-I, Hiroshi; Schwartz, Erik; Koepf, Matthieu; Vananroye, Anja; Vermant, Jan; Nolte, Roeland J M; De Schryver, Frans; Maan, Jan C; Hofkens, Johan; Christianen, Peter C M; Rowan, Alan E

    2016-01-26

    The thermal motion of polymer chains in a crowded environment is anisotropic and highly confined. Whereas theoretical and experimental progress has been made, typically only indirect evidence of polymer dynamics is obtained either from scattering or mechanical response. Toward a complete understanding of the complicated polymer dynamics in crowded media such as biological cells, it is of great importance to unravel the role of heterogeneity and molecular individualism. In the present work, we investigate the dynamics of synthetic polymers and the tube-like motion of individual chains using time-resolved fluorescence microscopy. A single fluorescently labeled polymer molecule is observed in a sea of unlabeled polymers, giving access to not only the dynamics of the probe chain itself but also to that of the surrounding network. We demonstrate that it is possible to extract the characteristic time constants and length scales in one experiment, providing a detailed understanding of polymer dynamics at the single chain level. The quantitative agreement with bulk rheology measurements is promising for using local probes to study heterogeneity in complex, crowded systems. PMID:26688072

  6. Non-strinking siloxane polymers

    Science.gov (United States)

    Loy, Douglas A.; Rahimian, Kamyar

    2001-01-01

    Cross-linked polymers formed by ring-opening polymerization of a precursor monomer of the general formula R[CH.sub.2 CH(Si(CH.sub.3).sub.2).sub.2 O].sub.2, where R is a phenyl group or an alkyl group having at least two carbon atoms. A cross-linked polymer is synthesized by mixing the monomer with a co-monomer of the general formula CH.sub.2 CHR.sup.2 (SiMe.sub.2).sub.2 O in the presence of an anionic base to form a cross-linked polymer of recurring units of the general formula R(Me.sub.2 SiOCH.sub.2 CHSiMe.sub.2).sub.2 [CH.sub.2 CHR.sup.2 (SiMe.sub.2).sub.2 O].sub.n, where R.sup.2 is hydrogen, phenyl, ethyl, propyl or butyl. If the precursor monomer is a liquid, the polymer can be directly synthesized in the presence of an anionic base to a cross-linked polymer containing recurring units of the general formula R(Me.sub.2 SiOCH.sub.2 CHSiMe.sub.2).sub.2. The polymers have approximately less than 1% porosity and are thermally stable at temperatures up to approximately 500.degree. C. The conversion to the cross-linked polymer occurs by ring opening polymerization and results in shrinkage of less than approximately 5% by volume.

  7. Monitoring of polymer melt processing

    International Nuclear Information System (INIS)

    The paper reviews the state-of-the-art of in-line and on-line monitoring during polymer melt processing by compounding, extrusion and injection moulding. Different spectroscopic and scattering techniques as well as conductivity and viscosity measurements are reviewed and compared concerning their potential for different process applications. In addition to information on chemical composition and state of the process, the in situ detection of morphology, which is of specific interest for multiphase polymer systems such as polymer composites and polymer blends, is described in detail. For these systems, the product properties strongly depend on the phase or filler morphology created during processing. Examples for optical (UV/vis, NIR) and ultrasonic attenuation spectra recorded during extrusion are given, which were found to be sensitive to the chemical composition as well as to size and degree of dispersion of micro or nanofillers in the polymer matrix. By small-angle light scattering experiments, process-induced structures were detected in blends of incompatible polymers during compounding. Using conductivity measurements during extrusion, the influence of processing conditions on the electrical conductivity of polymer melts with conductive fillers (carbon black or carbon nanotubes) was monitored. (topical review)

  8. Elastic Behavior of Polymer Chains

    Institute of Scientific and Technical Information of China (English)

    Teng Lu; Tao Chen; Hao-jun Liang

    2008-01-01

    The elastic behavior of the polymer chain was investigated in a three-dimensional off-lattice model. We sample more than 109 conformations of each kind of polymer chain by using a Monte Carlo algorithm, then analyze them with the non-Gaussian theory of rubberlike elasticity, and end with a statistical study. Through observing the effect of the chain flexibility and the stretching ratio on the mean-square end-to-end distance,the average energy, the average Helmholtz free energy, the elastic force, the contribution of energy to the elastic force, and the entropy contribution to elastic force of the polymer chain, we find that a rigid polymer chain is much easier to stretch than a flexible polymer chain. Also, a rigid polymer chain will become difficult to stretch only at a quite high stretching ratio because of the effect of the entropy contribution.These results of our simulation calculation may explain some of the macroscopic phenomena of polymer and biomacromolecular elasticity.

  9. Physical properties of polymers handbook

    CERN Document Server

    2007-01-01

    This book offers concise information on the properties of polymeric materials, particularly those most relevant to physical chemistry and chemical physics. Extensive updates and revisions to each chapter include eleven new chapters on novel polymeric structures, reinforcing phases in polymers, and experiments on single polymer chains. The study of complex materials is highly interdisciplinary, and new findings are scattered among a large selection of scientific and engineering journals. This book brings together data from experts in the different disciplines contributing to the rapidly growing area of polymers and complex materials.

  10. Multilayer Electroactive Polymer Composite Material

    Science.gov (United States)

    Ounaies, Zoubeida (Inventor); Park, Cheol (Inventor); Harrison, Joycelyn S. (Inventor); Holloway, Nancy M. (Inventor); Draughon, Gregory K. (Inventor)

    2011-01-01

    An electroactive material comprises multiple layers of electroactive composite with each layer having unique dielectric, electrical and mechanical properties that define an electromechanical operation thereof when affected by an external stimulus. For example, each layer can be (i) a 2-phase composite made from a polymer with polarizable moieties and an effective amount of carbon nanotubes incorporated in the polymer for a predetermined electromechanical operation, or (ii) a 3-phase composite having the elements of the 2-phase composite and further including a third component of micro-sized to nano-sized particles of an electroactive ceramic incorporated in the polymer matrix.

  11. Statistical properties of curved polymer

    Indian Academy of Sciences (India)

    Surya Kanta Ghosh; Anirban Sain

    2008-08-01

    Intrinsic curvature of biopolymers is emerging as an essential feature in various biological phenomena. Examples of polymers with intrinsic curvature are microtubule in eukaryotic cells or FtsZ filaments in prokaryotic cells. We consider the general model for polymers with intrinsic curvature. We aim to study both equilibrium and dynamic properties of such polymers. Here we report preliminary results on the equilibrium distribution function $P({\\mathbf{R}})$ of the end-to-end distance ${\\mathbf{R}}$. We employ transfer matrix method for this study.

  12. Physics of photorefraction in polymers

    CERN Document Server

    West, Dave

    2004-01-01

    Photorefractive polymer composites are an unusually sensitive class of photopolymers. Physics of Photorefraction in Polymers describes our current understanding of the physical processes that produce a photorefractive effect in key composite materials. Topics as diverse as charge generation, dispersive charge transport, charge compensation and trapping, molecular diffusion, organic composite structure, and nonlinear optical wave coupling are all developed from a physical perspective. Emphasis is placed on explaining how these physical processes lead to observable properties of the polymers, and the authors discuss various applications, including holographic archiving.

  13. Metal-containing conducting polymers

    Energy Technology Data Exchange (ETDEWEB)

    Higgins, S. (Dept. of Chemistry, Univ. of St. Andrews, Fife (United Kingdom)); Crayston, J.A. (Dept. of Chemistry, Univ. of St. Andrews, Fife (United Kingdom))

    1993-03-22

    Poly-(2,6-di-(2-thienyl) pyridine) was investigated for its ability to complex to metals via the pyridine group. Ag[sup +], Cu[sup 2+] and Pd[sup 2+] were reducible in MeCN at the polymer coated electrode after it had been activated by cathodic potentials. The polymer was insulating in aqueous media but in MeCN the cation Ru[sub 3]O(OAc)[sub 6](py)[sub 2](MeOH)[sup +], py=pyridine, was adsorbed onto the polymer as a monolayer. (orig.)

  14. Bioderadable Polymers in Food Packaging

    Directory of Open Access Journals (Sweden)

    P.A.Pawar

    2013-01-01

    Full Text Available In recent years, there has been a marked increase in the interest in use of biodegradable materials in packaging. The principal function of packaging is protection and preservation of food from external contamination. This function involves retardation of deterioration, extension of shelf life, and maintenance of quality and safety of packaged food. Biodegradable polymers are the one which fulfill all these functions without causing any threat to the environment. The belief is that biodegradable polymer materials will reduce the need for synthetic polymer production (thus reducing pollution at a low cost, thereby producing a positive effect both environmentally and economically.

  15. Thermoresponsive Polymers for Biomedical Applications

    Directory of Open Access Journals (Sweden)

    Theoni K. Georgiou

    2011-08-01

    Full Text Available Thermoresponsive polymers are a class of “smart” materials that have the ability to respond to a change in temperature; a property that makes them useful materials in a wide range of applications and consequently attracts much scientific interest. This review focuses mainly on the studies published over the last 10 years on the synthesis and use of thermoresponsive polymers for biomedical applications including drug delivery, tissue engineering and gene delivery. A summary of the main applications is given following the different studies on thermoresponsive polymers which are categorized based on their 3-dimensional structure; hydrogels, interpenetrating networks, micelles, crosslinked micelles, polymersomes, films and particles.

  16. Wetting of brushes by polymer melts

    NARCIS (Netherlands)

    Maas, J.

    2001-01-01

    The scientific and practical importance of thin polymer films is evident and in many applications polymer films are required. Hence, studying properties of polymer films is relevant. Adsorption of polymer at liquid/solid interfaces can stabilise particles in a matrix. Homopolymers are often used for

  17. Carbon dioxide foaming of glassy polymers

    NARCIS (Netherlands)

    Wessling, M.; Borneman, Z.; Boomgaard, van den Th.; Smolders, C.A.

    1994-01-01

    The mechanism of foaming a glassy polymer using sorbed carbon dioxide is studied in detail. A glassy polymer supersaturated with nitrogen forms a microcellular foam, if the polymer is quickly heated above its glass transition temperature. A glassy polymer supersaturated with CO2 forms this foam-like

  18. Migration and sensory evaluation of irradiated polymers

    NARCIS (Netherlands)

    Stoffers, N.H.; Linssen, J.P.H.; Franz, R.; Welle, F.

    2004-01-01

    The effects on ionising irradiation on polymer additives, monomers and polymers themselves have been investigated. Changes of initial concentrations of certain additives and monomers, a change in their specific migration as well as sensory changes of the polymers were examined. Polymer stabilizers s

  19. Carbon nanotube-polymer composite actuators

    Science.gov (United States)

    Gennett, Thomas; Raffaelle, Ryne P.; Landi, Brian J.; Heben, Michael J.

    2008-04-22

    The present invention discloses a carbon nanotube (SWNT)-polymer composite actuator and method to make such actuator. A series of uniform composites was prepared by dispersing purified single wall nanotubes with varying weight percents into a polymer matrix, followed by solution casting. The resulting nanotube-polymer composite was then successfully used to form a nanotube polymer actuator.

  20. The Workshop on Conductive Polymers: Final Report

    Science.gov (United States)

    1985-10-01

    Reports are made by groups on: polyacetylene, polyphenylene, polyaniline, and related systems; molecular, crystallographic, and defect structures in conducting polymers; heterocyclic polymers; synthesis of new and improved conducting polymers; future applications possibilities for conducting polymers; and challenges for improved understanding of properties. (DLC)

  1. Method for bonding a thermoplastic polymer to a thermosetting polymer component

    NARCIS (Netherlands)

    Van Tooren, M.J.L.

    2012-01-01

    The invention relates to a method for bonding a thermoplastic polymer to a thermosetting polymer component, the thermoplastic polymer having a melting temperature that exceeds the curing temperature of the thermosetting polymer. The method comprises the steps of providing a cured thermosetting polym

  2. Extendability of Equilibria of Nematic Polymers

    Directory of Open Access Journals (Sweden)

    Hongyun Wang

    2008-01-01

    Full Text Available The purpose of this paper is to study the extendability of equilibrium states of rodlike nematic polymers with the Maier-Saupe intermolecular potential. We formulate equilibrium states as solutions of a nonlinear system and calculate the determinant of the Jacobian matrix of the nonlinear system. It is found that the Jacobian matrix is nonsingular everywhere except at two equilibrium states. These two special equilibrium states correspond to two points in the phase diagram. One point is the folding point where the stable prolate branch folds into the unstable prolate branch; the other point is the intersection point of the nematic branch and the isotropic branch where the unstable prolate state becomes the unstable oblate state. Our result establishes the existence and uniqueness of equilibrium states in the presence of small perturbations away from these two special equilibrium states.

  3. Polymer and Polymer Gel of Liquid Crystalline Semiconductors

    Institute of Scientific and Technical Information of China (English)

    Teppei Shimakawa; Naoki Yoshimoto; Jun-ichi Hanna

    2004-01-01

    It prepared a polymer and polymer gel of a liquid crystalline (LC) semiconductor having a 2-phenylnaphthalene moiety and studied their charge carrier transport properties by the time-of-flight technique. It is found that polyacrylate having the mesogenic core moiety of 2-phenylnaphtalene (PNP-acrylate) exhibited a comparable mobility of 10-4cm2/Vs in smectic A phase to those in smectic A (SmA) phase of small molecular liquid crystals with the same core moiety, e.g., 6-(4'-octylphenyl)- 2-dodecyloxynaphthalene (8-PNP-O12), and an enhanced mobility up to 10-3cm2/Vs in the LC-glassy phase at room temperature, when mixed with a small amount of 8-PNP-O12. On the other hand, the polymer gel consisting of 20 wt %-hexamethylenediacrylate (HDA)-based cross-linked polymer and 8-PNP-O12 exhibited no degraded mobility when cross-linked at the mesophase. These results indicate that the polymer and polymer composite of liquid crystalline semiconductors provide us with an easy way to realize a quality organic semiconductor thin film for the immediate device applications.

  4. New developments in thermally stable polymers

    Science.gov (United States)

    Hergenrother, Paul M.

    1991-01-01

    Advances in high-temperature polymers since 1985 are discussed with the emphasis on the chemistry. High-temperature polymers refer to materials that exhibit glass-transition temperatures greater than 200 C and have the chemical structure expected to provide high thermooxidative stability. Specific polymers or series of polymers were selected to show how the chemical structure influences certain properties. Poly(arylene ethers) and polyimides are the two principal families of polymers discussed. Recent work on poly(arylene ethers) has concentrated on incorporating heterocyclic units within the polymer backbone. Recent polyimide work has centered on the synthesis of new polymers from novel monomers, several containing the trifluoromethyl group strategically located on the molecule. Various members in each of these polymer families display a unique combination of properties, heretofore unattainable. Other families of polymers are also briefly discussed with a polymer from an AB maleimidobenzocyclobutene exhibiting an especially attractive combination of properties.

  5. Recent advances in photorefractive polymers

    Science.gov (United States)

    Thomas, Jayan; Christenson, C. W.; Lynn, B.; Blanche, P.-A.; Voorakaranam, R.; Norwood, R. A.; Yamamoto, M.; Peyghambarian, N.

    2011-10-01

    Photorefractive composites derived from conducting polymers offer the advantage of dynamically recording holograms without the need for processing of any kind. Thus, they are the material of choice for many cutting edge applications, such as updatable three-dimensional (3D) displays and 3D telepresence. Using photorefractive polymers, 3D images or holograms can be seen with the unassisted eye and are very similar to how humans see the actual environment surrounding them. Absence of a large-area and dynamically updatable holographic recording medium has prevented realization of the concept. The development of a novel nonlinear optical chromophore doped photoconductive polymer composite as the recording medium for a refreshable holographic display is discussed. Further improvements in the polymer composites could bring applications in telemedicine, advertising, updatable 3D maps and entertainment.

  6. Conducting polymer 3D microelectrodes

    DEFF Research Database (Denmark)

    Sasso, Luigi; Vazquez, Patricia; Vedarethinam, Indumathi;

    2010-01-01

    Conducting polymer 3D microelectrodes have been fabricated for possible future neurological applications. A combination of micro-fabrication techniques and chemical polymerization methods has been used to create pillar electrodes in polyaniline and polypyrrole. The thin polymer films obtained...... showed uniformity and good adhesion to both horizontal and vertical surfaces. Electrodes in combination with metal/conducting polymer materials have been characterized by cyclic voltammetry and the presence of the conducting polymer film has shown to increase the electrochemical activity when compared...... with electrodes coated with only metal. An electrochemical characterization of gold/polypyrrole electrodes showed exceptional electrochemical behavior and activity. PC12 cells were finally cultured on the investigated materials as a preliminary biocompatibility assessment. These results show that the described...

  7. SCATTERING FUNCTION OF POLYMER BLENDS

    Institute of Scientific and Technical Information of China (English)

    Lin-ping Ke; Mei-li Guo; De-lu Zhao

    2004-01-01

    For a system of flexible polymer molecules, the concepts of two concentrations, namely the segmental and the molecular concentrations, have been proposed in this paper. The former is equivalent to the volume fraction. The latter can be defined as the number of the gravity centers of macromolecules in a unit volume. The two concentrations should be correlated with each other by the conformational function of the polymer chain and should be discussed in different thermodynamic equations. On the basis of these concepts it has been proved that the Flory-Huggins entropy of mixing should be the result of the mixing "ideal gases of the gravity centers of macromolecules". The general correlation between the free energy of mixing and the scattering function (structural factor) of polymer blends has been studied based on the general fluctuation theory. When the Flory-Huggins free energy of mixing is adopted, the de Gennes scattering function of a polymer blend can be derived.

  8. Deformation of Linked Polymer Coils

    Institute of Scientific and Technical Information of China (English)

    董朝霞; 李明远; 吴肇亮; 林梅钦

    2003-01-01

    Linked polymer solution (LPS) is defined as the solution of linked polymer coils (LPCs) dispersed in water, composed of low concentration partially hydrolyzed polyacrylamide (HPAM) and aluminum citrate (crosslinker). In the work, the conformational changes of LPCs under different conditions were investigated by the methods of membrane filtering under low pressure, dynamic light scattering and core flooding experiments. The results showed that in some conditions the LPCs could be compressed mechanically to 1/158.5 of their original volume because of relatively lower HPAM cross-linking. The hydration property of LPCs was similar to that of normal polymer coils. The deformation of LPCs was more restricted than that of ordinary polymer coils under the flow shear stress or the shift of hydration equilibrium caused in the variation of the electrolyte concentration which is responsible for the effective plugging in the throats of porous media when LPCs are used for deep diverting.

  9. Light-emitting polymer LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Moratti, S.C.; Bradley, D.D.C.; Cervini, R.; Friend, R.H.; Greenham, N.C.; Holmes, A.B. [Univ. of Cambridge (United Kingdom)

    1994-12-31

    Simple light emitting diodes can be constructed using fluorescent organic materials. Conjugated polymers can be used both for charge transport and for light emission. It is considered necessary for maximum device efficiency to balance the rates of electron and hole injection. The authors report the synthesis of a poly(cyanoterephthalylidenene) that was designed to exhibit an increased electron affinity. Electrochemical measurements showed a significant shift in the oxidation and reduction potentials due to the cyano functionality. The use of this polymer in a range of electroluminescent devices is described. Internal quantum efficiencies of up to 4% can be achieved in a bilayer device using stable electrode materials. The route used to synthesize this polymer is amenable to considerable variation in the subunits employed. This allows tuning of both the band-gap and the electron affinity of the resulting polymer.

  10. Conducting Polymers: Emerging Commercial Materials

    Directory of Open Access Journals (Sweden)

    N. Kumar

    1996-04-01

    Full Text Available Conducting polymers are materials of recent origin. They are obtained by polymerisation of simple organic monomers and doping with electron acceptor or donor species and show conductivity ranging from that of a semiconductor to that of metal. These materials are now available with unique electronic and optical properties of metals and semiconductors in combination with the attractive mechanical and processable advantages of polymers. The field has progressed to a level of maturity consistent with a new set of opportunities to develop Wide range of applications based upon conducting polymers as materials for industrial products.Examples include: static charge dissipation, EMI shielding, flexible light emitting diodes, transparent electrodes, batteries, gas sensors, gas separators, etc. Many of the conducting polymers and devices based on them are now available commercially.

  11. Polymer electronic devices and materials.

    Energy Technology Data Exchange (ETDEWEB)

    Schubert, William Kent; Baca, Paul Martin; Dirk, Shawn M.; Anderson, G. Ronald; Wheeler, David Roger

    2006-01-01

    Polymer electronic devices and materials have vast potential for future microsystems and could have many advantages over conventional inorganic semiconductor based systems, including ease of manufacturing, cost, weight, flexibility, and the ability to integrate a wide variety of functions on a single platform. Starting materials and substrates are relatively inexpensive and amenable to mass manufacturing methods. This project attempted to plant the seeds for a new core competency in polymer electronics at Sandia National Laboratories. As part of this effort a wide variety of polymer components and devices, ranging from simple resistors to infrared sensitive devices, were fabricated and characterized. Ink jet printing capabilities were established. In addition to promising results on prototype devices the project highlighted the directions where future investments must be made to establish a viable polymer electronics competency.

  12. Conjugated Polymers for Energy Production

    DEFF Research Database (Denmark)

    Livi, Francesco

    This dissertation is aimed at developing materials for flexible, large area, ITO-free polymer solar cells (PSCs) fully printed under ambient conditions. A large screening of conjugated polymers, both novel and well-known materials, has been carried out in order to find suitable candidates...... for scalable PSCs fully printed under ambient conditions [Adv. Energy Mater. 2015, 5, 1402186]. PPDTBT resulted to be the conjugated polymer with the best photovoltaic performance within the 104 synthesized macromolecules. Therefore, further studies have been done on such material. The impact of side chain...... arylation (DAr) and direct arylation polymerization (DArP) have been applied to the preparation of PPDTBT, making this polymer readily available in only 4 synthetic steps and thus easily transferable to a large scale-production setup. DArP avoids organometallic species and therefore is an appealing...

  13. Color Changes Mark Polymer Reactions.

    Science.gov (United States)

    Krieger, James H.

    1980-01-01

    Describes how polydiacetylenes can be used as educational aids. These polymers have conjugated backbones, which cause changes in color when the polydiacetylenes undergo various chemical and physical processes. Diagrams summarize all chemical reactions and their associated color changes. (CS)

  14. Modeling the polymer product maceration

    Science.gov (United States)

    Ahunov, D. N.; Karpova, M. N.

    2014-12-01

    The article contains a view of mass transmission simulation procedure conformably to control of manufacturing method's automation, and also is shown a simulator of polymer product maceration process, and results of developed for this simulator realization program system

  15. Finely divided, irradiated tetrafluorethylene polymers

    International Nuclear Information System (INIS)

    Dry non-sticky fine lubricant powders are made by γ-irradiation of unsintered coagulated dispersion grade tetrafluoroethylene polymers. These powders may also be dispersed in an organic medium for lubricating purposes

  16. Sonochemical Preparation of Polymer Nanocomposites

    Directory of Open Access Journals (Sweden)

    Hyoung Jin Choi

    2009-06-01

    Full Text Available Thisreview covers sonochemical fabrication of polymer nanocomposites. In addition to its application to the synthesis of various polymeric systems, due to its powerful efficiency, sonochemistry has been widely used not only as the assistant of dispersion for nanomaterials such as carbon nanotubes (CNT and organophillic clay, but also as a special initiator to enhance polymerization for fabrication of polymer nanocomposites with CNT and metallic nanoparticles. Recent developments in the preparation of multi-walled carbon nanotube/polymer nanocomposites with polystyrene and PMMA, magnetic particle/CNT composites and polymer/clay nanocomposites along with their physical characteristics and potential engineering applications will be introduced. Physical characterizations include morphological, thermal, and rheological properties under either an applied electric or magnetic field.

  17. Conducting Polymer 3D Microelectrodes

    Directory of Open Access Journals (Sweden)

    Jenny Emnéus

    2010-12-01

    Full Text Available Conducting polymer 3D microelectrodes have been fabricated for possible future neurological applications. A combination of micro-fabrication techniques and chemical polymerization methods has been used to create pillar electrodes in polyaniline and polypyrrole. The thin polymer films obtained showed uniformity and good adhesion to both horizontal and vertical surfaces. Electrodes in combination with metal/conducting polymer materials have been characterized by cyclic voltammetry and the presence of the conducting polymer film has shown to increase the electrochemical activity when compared with electrodes coated with only metal. An electrochemical characterization of gold/polypyrrole electrodes showed exceptional electrochemical behavior and activity. PC12 cells were finally cultured on the investigated materials as a preliminary biocompatibility assessment. These results show that the described electrodes are possibly suitable for future in-vitro neurological measurements.

  18. Polymer Bose–Einstein condensates

    Energy Technology Data Exchange (ETDEWEB)

    Castellanos, E., E-mail: ecastellanos@fis.cinvestav.mx [Departamento de Física, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, A.P. 14-740, México D.F. 07000 (Mexico); Chacón-Acosta, G., E-mail: gchacon@correo.cua.uam.mx [Departamento de Matemáticas Aplicadas y Sistemas, Universidad Autónoma Metropolitana-Cuajimalpa, Artificios 40, México D.F. 01120 (Mexico)

    2013-05-13

    In this work we analyze a non-interacting one-dimensional polymer Bose–Einstein condensate in a harmonic trap within the semiclassical approximation. We use an effective Hamiltonian coming from the polymer quantization that arises in loop quantum gravity. We calculate the number of particles in order to obtain the critical temperature. The Bose–Einstein functions are replaced by series, whose high order terms are related to powers of the polymer length. It is shown that the condensation temperature presents a shift respect to the standard case, for small values of the polymer scale. In typical experimental conditions, it is possible to establish a bound for λ{sup 2} up to ≲10{sup −16} m{sup 2}. To improve this bound we should decrease the frequency of the trap and also decrease the number of particles.

  19. Conductive polymer-based material

    Science.gov (United States)

    McDonald, William F.; Koren, Amy B.; Dourado, Sunil K.; Dulebohn, Joel I.; Hanchar, Robert J.

    2007-04-17

    Disclosed are polymer-based coatings and materials comprising (i) a polymeric composition including a polymer having side chains along a backbone forming the polymer, at least two of the side chains being substituted with a heteroatom selected from oxygen, nitrogen, sulfur, and phosphorus and combinations thereof; and (ii) a plurality of metal species distributed within the polymer. At least a portion of the heteroatoms may form part of a chelation complex with some or all of the metal species. In many embodiments, the metal species are present in a sufficient concentration to provide a conductive material, e.g., as a conductive coating on a substrate. The conductive materials may be useful as the thin film conducting or semi-conducting layers in organic electronic devices such as organic electroluminescent devices and organic thin film transistors.

  20. Polyphosphazine-based polymer materials

    Science.gov (United States)

    Fox, Robert V.; Avci, Recep; Groenewold, Gary S.

    2010-05-25

    Methods of removing contaminant matter from porous materials include applying a polymer material to a contaminated surface, irradiating the contaminated surface to cause redistribution of contaminant matter, and removing at least a portion of the polymer material from the surface. Systems for decontaminating a contaminated structure comprising porous material include a radiation device configured to emit electromagnetic radiation toward a surface of a structure, and at least one spray device configured to apply a capture material onto the surface of the structure. Polymer materials that can be used in such methods and systems include polyphosphazine-based polymer materials having polyphosphazine backbone segments and side chain groups that include selected functional groups. The selected functional groups may include iminos, oximes, carboxylates, sulfonates, .beta.-diketones, phosphine sulfides, phosphates, phosphites, phosphonates, phosphinates, phosphine oxides, monothio phosphinic acids, and dithio phosphinic acids.

  1. Cyclodextrin Inclusion Polymers Forming Hydrogels

    Science.gov (United States)

    Li, Jun

    This chapter reviews the advances in the developments of supramolecular hydrogels based on the polypseudorotaxanes and polyrotaxanes formed by inclusion complexes of cyclodextrins threading onto polymer chains. Both physical and chemical supramolecular hydrogels of many different types are discussed with respect to their preparation, structure, property, and gelation mechanism. A large number of physical supramolecular hydrogels were formed induced by self-assembly of densely packed cyclodextrin rings threaded on polymer or copolymer chains acting as physical crosslinking points. The thermo-reversible and thixotropic properties of these physical supramolecular hydrogels have inspired their applications as injectable drug delivery systems. Chemical supramolecular hydrogels synthesized from polypseudorotaxanes and polyrotaxanes were based on the chemical crosslinking of either the cyclodextrin molecules or the included polymer chains. The chemical supramolecular hydrogels were often made biodegradable through incorporation of hydrolyzable threading polymers, end caps, or crosslinkers, for their potential applications as biomaterials.

  2. Photosensitized oxidation of unsaturated polymers

    Science.gov (United States)

    Golub, M. A.

    1980-01-01

    A review of the photosensitized oxidation of singlet oxygenation of unsaturated hydrocarbon polymers and of their model compounds is presented. The cis and trans forms of 1,4-polyisoprene, 1,4-polybutadiene and 1,2-poly(1,4-hexadiene) are studied, and their microstructural changes which occur on reaction with (IO2) in solution were investigated by infrared, (H-1) and (C-13) NMR spectroscopy. The polymers yielded allylic hydroperoxides with shifted double bonds according to the 'ene' mechanism of simple olefins. It was shown that single oxygenation of unsaturated polymers is similar to their low molecular weight analogs, and that the differences are due to secondary processes affecting the (IO2)-reacted polymers.

  3. Emergent tilt order in Dirac polymer liquids

    OpenAIRE

    Souslov, Anton; Loewe, Benjamin; Goldbart, Paul M.

    2014-01-01

    We study a liquid of zigzagging two-dimensional directed polymers with bending rigidity, i.e., polymers whose conformations follow checkerboard paths. In the continuum limit the statistics of such polymers obey the Dirac equation for particles of imaginary mass. We exploit this observation to investigate a liquid of these polymers via a quantum many-fermion analogy. A self-consistent approximation predicts a phase of tilted order, in which the polymers may develop a preference to zig rather t...

  4. Are Entangled Polymer Melts Different From Solutions?

    OpenAIRE

    Huang, Qian; Mednova, Olga; Rasmussen, Henrik K.; Skov, Anne Ladegaard; Almdal, Kristoffer; Hassager, Ole

    2012-01-01

    The possible existence of a qualitative difference on extensional steady state viscosity between polymer melts and polymer solutions is still an open question. Recent experiments [1-4] showed the extensional viscosity of both polymer melts and solutions decayed as a function of strain rate with an exponent of -0.5. When the strain rate became higher than the order of inverse Rouse time, the polymer solutions showed an upturn [1, 4]. However, in the same regime for polymer melts, the experimen...

  5. Physical Organic Chemistry of Supramolecular Polymers

    Science.gov (United States)

    Serpe, Michael J.; Craig, Stephen L.

    2008-01-01

    Unlike the case of traditional covalent polymers, the entanglements that determine properties of supramolecular polymers are defined by very specific, intermolecular interactions. Recent work using modular molecular platforms to probe the mechanisms underlying mechanical response of supramolecular polymers is reviewed. The contributions of supramolecular kinetics, thermodynamics, and conformational flexibility to supramolecular polymer properties in solutions of discrete polymers, in networks, and at interfaces, are described. Molecule-to-material relationships are established through methods reminiscent of classic physical organic chemistry. PMID:17279638

  6. Surface segregation of conformationally asymmetric polymer blends

    OpenAIRE

    Stepanow, Semjon; Fedorenko, Andrei A.

    2005-01-01

    We have generalized the Edwards' method of collective description of dense polymer systems in terms of effective potentials to polymer blends in the presence of a surface. With this method we have studied conformationally asymmetric athermic polymer blends in the presence of a hard wall to the first order in effective potentials. For polymers with the same gyration radius $R_g$ but different statistical segment lengths $l_{A}$ and $l_{B}$ the excess concentration of stiffer polymers at the su...

  7. Study about polymer applications in footwear

    OpenAIRE

    Khan, Majbaur

    2015-01-01

    This thesis was written to study polymer uses in footwear and to define engineered polymers in footwear. How and why polymers are used nowadays in footwear. Though leather is a prime material for footwear but polymers are used for their some properties which are suitable for footwear. It is also significant in this thesis the comparison of leather and polymers as a footwear material. To describe the classification and mechanism of adhesive those are used in this sector is also a very importan...

  8. Polymer-phyllosilicate nanocomposites and their preparation

    Science.gov (United States)

    Chaiko, David J.

    2007-01-09

    Polymer-phyllosilicate nanocomposites that exhibit superior properties compared to the polymer alone, and methods-for producing these polymer-phyllosilicate nanocomposites, are provided. Polymeric surfactant compatabilizers are adsorbed onto the surface of hydrophilic or natural phyllosilicates to facilitate the dispersal and exfoliation of the phyllosilicate in a polymer matrix. Utilizing polymeric glycol based surfactants, polymeric dicarboxylic acids, polymeric diammonium surfactants, and polymeric diamine surfactants as compatabilizers facilitates natural phyllosilicate and hydrophilic organoclay dispersal in a polymer matrix to produce nanocomposites.

  9. Wetting of brushes by polymer melts

    OpenAIRE

    Maas, J

    2001-01-01

    The scientific and practical importance of thin polymer films is evident and in many applications polymer films are required. Hence, studying properties of polymer films is relevant. Adsorption of polymer at liquid/solid interfaces can stabilise particles in a matrix. Homopolymers are often used for steric stabilisation of particles although these polymers can also destabilise the system by bridging. Diblock copolymers with one adsorbing (anchor) block and one non-adsorbing (buoy) block may b...

  10. Characterization of Tantalum Polymer Capacitors

    Science.gov (United States)

    Spence, Penelope

    2012-01-01

    Overview Reviewed data Caution must be taken when accelerating test conditions Data not useful to establish an acceleration model Introduction of new failure mechanism skewing results Evidence of Anti-Wear-Out De-doping of polymer Decreased capacitance Increased ESR Not dielectric breakdown Needs further investigation Further investigation into tantalum polymer capacitor technology Promising acceleration model for Manufacturer A Possibility for use in high-reliability space applications with suitable voltage derating.

  11. Thermodynamics of tubelike flexible polymers

    OpenAIRE

    Vogel, T.; Neuhaus, T; Bachmann, M.; Janke, W.

    2009-01-01

    In this work, we discuss the general phase behavior of short tubelike flexible polymers. The geometric thickness constraint is implemented through the concept of the global radius of curvature. We use sophisticated Monte Carlo sampling methods to simulate small bead-stick polymer models with Lennard-Jones interaction among nonbonded monomers. We analyze energetic fluctuations and structural quantities to classify conformational pseudophases. We find that the tube thickness influences the ther...

  12. Nanoporous polymer liquid core waveguides

    DEFF Research Database (Denmark)

    Gopalakrishnan, Nimi; Christiansen, Mads Brøkner; Ndoni, Sokol;

    2010-01-01

    We demonstrate liquid core waveguides defined by UV to enable selective water infiltration in nanoporous polymers, creating an effective refractive index shift Δn=0.13. The mode confinement and propagation loss in these waveguides are presented.......We demonstrate liquid core waveguides defined by UV to enable selective water infiltration in nanoporous polymers, creating an effective refractive index shift Δn=0.13. The mode confinement and propagation loss in these waveguides are presented....

  13. Conducting Polymers: Emerging Commercial Materials

    OpenAIRE

    Kumar, N; S. R. Vadera; Jeevan Singh; Das, G.; S. C. Negi; Aparna, P.; Tuli, A

    1996-01-01

    Conducting polymers are materials of recent origin. They are obtained by polymerisation of simple organic monomers and doping with electron acceptor or donor species and show conductivity ranging from that of a semiconductor to that of metal. These materials are now available with unique electronic and optical properties of metals and semiconductors in combination with the attractive mechanical and processable advantages of polymers. The field has progressed to a level of maturity cons...

  14. Supramolecular control over thermoresponsive polymers

    OpenAIRE

    Victor R. de la Rosa; Patrice Woisel; Richard Hoogenboom

    2016-01-01

    Thermoresponsive polymers facilitate the development of a wide range of applications in multiple areas spanning from construction or water management to lab-on-a-chip technologies and biomedical sciences. The combination of thermoresponsive polymers with supramolecular chemistry, inspired by the molecular mechanisms behind natural systems, is resulting in adaptive and smart materials with unprecedented properties. This work reviews the past advances on the combination of this young field of r...

  15. Biocompatible and Bioeliminable Hydrophilic Polymers

    Institute of Scientific and Technical Information of China (English)

    Paolo; FerrutiUniversità

    2007-01-01

    1 Introduction This presentation will report on some recent results obtained in Milan on two polymer families of biomedical interest, namely poly(N-vinyl-2-pyrrolidinone) and polyamidoamines. 2 Results and DiscussionPoly(N-vinyl-2-pyrrolidinone) (PVP) is a well known bioactive and biocompatible polymer. In its soluble form, it is largely used as excipient of oral pharmaceutical formulations, especially for its high water solubilising power.In its crosslinked form, it plays a relevant role as biomateria...

  16. Heterogeneity in Polymer Thin Films

    OpenAIRE

    Kanaya, Toshiji; Inoue, Rintaro; Nishida, Koji

    2011-01-01

    In the last two decades very extensive studies have been performed on polymer thin films to reveal very interesting but unusual properties. One of the most interesting findings is the decrease in glass transition temperature Tg with film thickness in polystyrene (PS) thin film supported on Si substrate. Another interesting finding is apparent negative thermal expansivity in glassy state for thin films below ∼25 nm. In order to understand the unusual properties of polymer thin films we have st...

  17. Radiation processing of natural polymer

    International Nuclear Information System (INIS)

    Radiation processing of natural polymer has been the subject of interest of countries in this region in the past 5 ∼ 7 years. Although some of the output of the research have been commercialized in particular for the applications in the agriculture and healthcare sectors, the potential applications of radiation processing of natural polymers in the medical sector are yet to be fully understood and developed. (author)

  18. Methods of polymer binder examination

    Directory of Open Access Journals (Sweden)

    M. Holtzer

    2010-10-01

    Full Text Available This article presents selected methods of examining polymer binders (in particular current or promising ones, including spectroscopy, microscopy, nanometry, chromatography and thermal analysis. The table (containing 23 literature references collates and generally characterises over 20 analytical methods from the above groups. In addition, information is presented on research conducted by the Environmental Protection Lab of the Chair of Casting Process Engineering, Faculty of Foundry Engineering, AGH University of Science and Technology concerning the physical chemistry of polymer casting binders.

  19. Polymer nanocomposites reinforced with montmorillonite

    OpenAIRE

    L.A. Dobrzański; M. Bilewicz; Viana, J. C.

    2012-01-01

    Purpose: Light microscope with polarized light has been used for observation layered zone, visible thanks to polarization of the light, inside polymer-polymer composites and nanocomposites Aim of work has been concentrated on investigation of nanocomposites as promising engineering materials, basing on composition of polypropylene and montmorillonite as reinforcement in the shape of nanoparticles of 2:1 silicate.Design/methodology/approach: Conventional and non-conventional injection molding ...

  20. Polymer compositions based on PXE

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Jin; Eitouni, Hany Basam; Singh, Mohit

    2015-09-15

    New polymer compositions based on poly(2,6-dimethyl-1,4-phenylene oxide) and other high-softening-temperature polymers are disclosed. These materials have a microphase domain structure that has an ionically-conductive phase and a phase with good mechanical strength and a high softening temperature. In one arrangement, the structural block has a softening temperature of about 210.degree. C. These materials can be made with either homopolymers or with block copolymers.

  1. Polymer nanocomposites reinforced with montmorillonite

    Directory of Open Access Journals (Sweden)

    L.A. Dobrzański

    2012-01-01

    Full Text Available Purpose: Light microscope with polarized light has been used for observation layered zone, visible thanks to polarization of the light, inside polymer-polymer composites and nanocomposites Aim of work has been concentrated on investigation of nanocomposites as promising engineering materials, basing on composition of polypropylene and montmorillonite as reinforcement in the shape of nanoparticles of 2:1 silicate.Design/methodology/approach: Conventional and non-conventional injection molding process has been used for obtaining nanocomposites. In non-conventional process has been used the special mold for inducing the shear rates, additionally equipped with external computer to control melt manipulation of solidifying polymer inside mold cavityFindings: Highly developed structure consisted of multilayer zone between skin and core mainly responsible for reinforcement and improvement of fracture toughness of polymer composites and nanocompositesResearch limitations/implications: Nanocomposites of polymer blends and montmorillonite were moulded by direct injection moulding according to melt temperature and stroke time-number combination included in design of experiments.Practical implications: Application of special injection moulding technique provides to structure development and gives possibility to create multilayer zone, which strengthen material. Besides strengthening obtaining of such nanocomposites is cheap thanks to application of low cost injection moulding technique and not expensive polyolefines with developed structure, without using additional fillers (e.g. compatybilizers.Originality/value: Very wide application of polymer composites and nanocomposites as engineering materials used for various industries like building engineering, automotive and aerospace

  2. Effects of nanoscopic-confinement on polymer dynamics.

    Science.gov (United States)

    Chrissopoulou, Kiriaki; Anastasiadis, Spiros H

    2015-05-21

    The static and dynamic behavior of polymers in confinement close to interfaces can be very different from that in the bulk. Among the various geometries, intercalated nanocomposites, in which polymer films of ∼1 nm thickness reside between the parallel inorganic surfaces of layered silicates in a well-ordered multilayer, offer a unique avenue for the investigation of the effects of nanoconfinement on polymer structure and dynamics by utilizing conventional analytical techniques and macroscopic specimens. In this article, we provide a review of research activities mainly in our laboratory on polymer dynamics under severe confinement utilizing different polymer systems: polar and non-polar polymers were mixed with hydrophilic or organophilic silicates, respectively, whereas hyperbranched polymers were studied in an attempt to probe the effect of polymer-surface interactions by altering the number and the kinds of functional groups in the periphery of the branched polymers. The polymer dynamics was probed by quasielastic neutron scattering and dielectric relaxation spectroscopy and was compared with that of the polymers in the bulk. In all cases, very local sub-Tg processes related to the motion of side and/or end groups as well as the segmental α-relaxation were identified with distinct differences recorded between the bulk and the confined systems. Confinement was found not to affect the very local motion in the case of the linear chains whereas it made it easier for hyperbranched polymers due to modifications of the hydrogen bond network. The segmental relaxation in confinement becomes faster than that in the bulk, exhibits Arrhenius temperature dependence and is observed even below the bulk Tg due to reduced cooperativity in the confined systems. PMID:25869864

  3. Towards Monodispersed Polymer Microspheres

    Science.gov (United States)

    Senuma, Yoshinori; Hilborn, Jons

    1998-03-01

    Uniform polymer microspheres prepared by Spinning Disk Atomization Our spinning disk atomization (SDA) can, relative to other existing techniques, produce micron-sized particles of very narrow size distribution. Around the edge of the disk, small teeth channel the flow into identical droplets that are flung off over the disk rim. These solidify during flight to form spherical particles. Applications for spheres produced by SDA can be found in areas such as adhesives, powder coatings, food, biomedical use, drug delivery systems, etc. We have atomized polyethyleneglycol into very narrowly dispersed microspheres ranging from 50 to 500 =B5m. The aim of this work is to model the droplet formation occurring at the rim of the spinning disk in order to better understand the experimental results. The viscosity contribution in the fluid breakup is qualitatively analyzed and is adapted to the theoretical model to show how it affects the droplet size. We have used the pendant drop model (Ramesh Babu, S. Journal of Colloid and Interface Science 116, 350-372 (1987).) for spinning disk atomization to describe the drop-shape evolution during growth.

  4. Synthesis, dynamic properties and electrochemical stability of organic-inorganic hybrid polymer electrolytes with double core branched structures based on polyether, cyanuric chloride and alkoxysilane

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • New cyanuric chloride based double-core solid hybrid electrolyte is synthesized. • Conductivity of the hybrid electrolyte follows Vogel-Tamman-Fulcher behavior. • Hybrid electrolyte possesses maximum ionic conductivity of 9.5 × 10−5 Scm−1 at 30 °C. • PGSE NMR reveals ion pairs and segmental mobility affect Li diffusion coefficient. • Two local environments are identified for Li+ ions in the hybrid electrolyte. - Abstract: A new organic-inorganic solid hybrid electrolyte based on 2,4,6-trichloro-1,3,5-triazine, triblock co-polymer poly(propylene glycol)-block-poly(ethylene glycol)-block-poly(propylene glycol) bis(2-aminopropyl ether), poly(ethylene glycol) diglycidyl ether, and 3-(glycidyloxypropyl)trimethoxysilane doped with LiClO4 salt is synthesized by a sol-gel process. Fourier transform infrared spectroscopy and 13C NMR results reveal the successful synthesis of the organic-inorganic hybrid electrolyte. The conductivity of the hybrid electrolyte follows a VTF (Vogel-Tamman-Fulcher)-like behavior, implying that the diffusion of charge carriers is assisted by the segmental motions of polymer chains. The Li-ion mobility is determined from 7Li static NMR linewidth and diffusion coefficient measurements; both are correlated with their ionic conductivities. The maximum ionic conductivity of 9.5 × 10−5 S cm−1 at 30 °C is obtained for the hybrid electrolyte with the [O]/[Li] ratio of 32. The electrochemical stability window of 4 V ensures the hybrid electrolyte as a potential candidate for low voltage lithium ion batteries

  5. LIQUID-LIQUID PHASE EQUILIBRIUM OF POLYMER SOLUTIONS AND POLYMER BLENDS UNDER POSITIVE AND NEGATIVE PRESSURE

    Institute of Scientific and Technical Information of China (English)

    Attila R.Imre

    2003-01-01

    In this paper we would like to give a brief review about the extensibility of the liquid-liquid locus into the negative pressure region. Negative pressure states are hardly explored; most researchers believe that the pressure scale ends at p = 0.We would like to show that this is not true, thep = 0 point is not a special point for liquids, it can be "easily" crossed. We are going to give a few example, where the extension of liquid-liquid locus for polymer blends and solutions below p = 0 gives us some interesting results, like the merging of UCST and LCST branches in weakly interacting polymer solutions or the reason why most UCST blends exhibit pressure induced immiscibility. Also, we will see what happens with the immiscibility island of aqueous polymer solutions when - reaching the critical molar mass - it "disappears".

  6. LIQUID—LIQUID PHASE EQUILIBRIUM OF POLYMER SOLUTIONS AND POLYMER BLENDS UNDER POSITIVE AND NEGATIVE PRESSURE

    Institute of Scientific and Technical Information of China (English)

    AttilaR.Imre

    2003-01-01

    In this paper we would like to give a brief review about the extensibility of the liquid-liquid locus into the negative pressure region.Negative pressure states are hardly explored;most researchers believe that the pressure scale ends at p=0. We would like to show that this is not true3 the p=0 point is not a special point for liquids,it can be “easily” crossed.We are going to give a few example,where the extension of liquid-liquid locus for polymer blends and solutions below p=0 gives us some interesting results,like the merging of UCST and LCST branches in weakly interacting polymer solutions or the reason why most UCST blends exhibit pressure induced immiscibility.Also,we will see what happens with the immiscibility island of aqueous polymer solutions when-reaching the critical molar mass-it “disappears”.

  7. Efficiency Improvement of Heterojunction Polymer Photovoltaic Cells through Controlling the Morphology of the Polymer Film

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    1 Results Polymer photovoltaic cells, which provide clean and renewable energy sources, have gained more and more attention. Polymer photovoltaic cells have the advantage of low fabrication cost and high mechanical flexibility. Polymers can be processed through a solution process, so that a homogeneous polymer film could be readily prepared in a large area. Recently, the light-to-electricity conversion efficiency of the polymer photovoltaic cells was improved significantly[1-2]. Polymer donor and organi...

  8. Precise Analysis of Polymer Rotational Dynamics

    Science.gov (United States)

    Kim, Jun Mo; Baig, Chunggi

    2016-01-01

    Through the analysis of individual chain dynamics alongside the corresponding molecular structures under shear via nonequilibrium molecular dynamics simulations of C178H358 linear and short-chain branched polyethylene melts under shear flow, we observed that the conventional method based on the chain end-to-end vector (and/or the gyration tensor of chain) is susceptible to quantitatively inaccurate measurements and often misleading information in describing the rotational dynamics of polymers. Identifying the flaw as attributed to strong irregular Brownian fluctuations inherent to the chain ends associated with their large free volume and strong molecular collisions, we propose a simple, robust way based on the chain center-to-center vector connecting the two centers of mass of the bisected chain, which is shown to adequately describe polymer rotational dynamics without such shortcomings. We present further consideration that the proposed method can be useful in accurately measuring the overall chain structure and dynamics of polymeric materials with various molecular architectures, including branched and ring polymers.

  9. Dihydroxybenzene/benzoquinone-containing polymers: organic redox polymers

    Energy Technology Data Exchange (ETDEWEB)

    Moulay, S. [Universite de Blida, Lab. de Chimie-Physique Macromoleculaire, Institut de Chimie Industrielle (Algeria)

    2000-08-01

    Polymers containing hydroquinone, catechol or their corresponding benzoquinones are a special class of redox polymers. Three pathways of their syntheses are possible: condensation polymerization of suitable monomers, addition polymerization of vinyl monomers containing redox moiety, and chemical attachment of redox unit onto pre-made polymeric matrix. A range of functionalized matrices have been employed such as polyethers, polyesters, polycarbonates, polyurethanes, polyamides and others. Protection of their phenolic functionality has conducted to chemically interesting redox polymer precursors. The presence of a redox moiety coupled with the extant functionalization of the polymer matrix makes the materials very valuable, of wide properties and consequently of vast applicability. For instance, in the oil field, some polymers such as carboxy-methyl-cellulose (CMC) are often applied as to bring about a viscosity improvement and therefore to facilitate the oil drilling. In this regard, Patel evaluated sulfo-alkylated polymeric catechol, namely sulfo-methylated and sulfo-ethylated resins. Indeed, polymeric catechol chemically modified as such exhibited a marked ability to control the viscosity, the gel strength, as well as the filtrate loss of aqueous oil drilling fluids.

  10. Polymer Stamps for Imprinting Nanopatterns in Polymer Substrate.

    Science.gov (United States)

    Wu, Jiahao; Amirsadeghi, Alborz; Kim, Jinsoo; Park, Sunggook

    2015-01-01

    Using a silicone or metallic stamp for imprinting multiscale patterns comprising micro down to nanoscale patterns into polymer substrates often results in significant deformation in the molded substrate and loss of pattern transfer fidelity for nanopatterns. In the worst case, the expensive stamp can also be damaged. One method to reduce the problem is to use polymer as the stamp material, which will reduce both adhesion and thermal stress generated at the stamp/substrate interface. In this paper, stamps made of three different polymer materials, i.e., polydimethylsiloxane (PDMS), PPGDA-based UV resin and TPGDA-based UV-resin, were fabricated from the same master containing nanofluidic structures and the replication fidelity from the master, polymer stamps, to thermal-imprinted poly(methyl methacrylate) substrate (PMMA) was compared. The largest loss of pattern fidelity occurs in the thermal imprinting step. Polymer stamps with higher Young's moduli result in a better fidelity in pattern transfer. With TPGDA-based UV resin stamps, multiscale structures with a nanochannel with minimum width and height of -70 nm can be imprinted onto PMMA substrate together with macro-scale patterns by a single nanoimprinting processes. PMID:26328384

  11. Quantitative equivalence between polymer nanocomposites and thin polymer films.

    Science.gov (United States)

    Bansal, Amitabh; Yang, Hoichang; Li, Chunzhao; Cho, Kilwon; Benicewicz, Brian C; Kumar, Sanat K; Schadler, Linda S

    2005-09-01

    The thermomechanical responses of polymers, which provide limitations to their practical use, are favourably altered by the addition of trace amounts of a nanofiller. However, the resulting changes in polymer properties are poorly understood, primarily due to the non-uniform spatial distribution of nanoparticles. Here we show that the thermomechanical properties of 'polymer nanocomposites' are quantitatively equivalent to the well-documented case of planar polymer films. We quantify this equivalence by drawing a direct analogy between film thickness and an appropriate experimental interparticle spacing. We show that the changes in glass-transition temperature with decreasing interparticle spacing for two filler surface treatments are quantitatively equivalent to the corresponding thin-film data with a non-wetting and a wetting polymer-particle interface. Our results offer new insights into the role of confinement on the glass transition, and we conclude that the mere presence of regions of modified mobility in the vicinity of the particle surfaces, that is, a simple two-layer model, is insufficient to explain our results. Rather, we conjecture that the glass-transition process requires that the interphase regions surrounding different particles interact. PMID:16086021

  12. Nanostructured polymer membranes for proton conduction

    Science.gov (United States)

    Balsara, Nitash Pervez; Park, Moon Jeong

    2013-06-18

    Polymers having an improved ability to entrain water are characterized, in some embodiments, by unusual humidity-induced phase transitions. The described polymers (e.g., hydrophilically functionalized block copolymers) have a disordered state and one or more ordered states (e.g., a lamellar state, a gyroid state, etc.). In one aspect, the polymers are capable of undergoing a disorder-to-order transition while the polymer is exposed to an increasing temperature at a constant relative humidity. In some aspects the polymer includes a plurality of portions, wherein a first portion forms proton-conductive channels within the membrane and wherein the channels have a width of less than about 6 nm. The described polymers are capable of entraining and preserving water at high temperature and low humidity. Surprisingly, in some embodiments, the polymers are capable of entraining greater amounts of water with the increase of temperature. The polymers can be used in Polymer Electrolyte Membranes in fuel cells.

  13. Free radical transfer in polymers

    International Nuclear Information System (INIS)

    For the present study of free-radical transfer in polymers pulse radiolysis and product studies have been carried out in aqueous solutions using thus far only the water-soluble polymers polyacrylic acid, polymethacrylic acid and polyvinyl alcohol. When OH radicals, generated in the radiolysis of N2O-saturated aqueous solutions, react with polymers the lifetime of the polymer radical thus created very much depends on the number of radicals per polymer chain. When there are a large number of radicals per chain their bimolecular decay may be faster than the corresponding (diffusion controlled) decay of monomeric radicals, but when the macromolecule contains only few or even just one radical their lifetime is considerably prolonged. Highly charged polymers such as polyacrylic acid at high pH attain a rod-like conformation which again favors a long lifetime of the radicals. Under such conditions, radical transfer reactions can occur. For example, in polyacrylic acid OH radicals generate two kinds of radicals side by side. The radical in β-position to the carboxylate group converts into the thermodynamically more stable α-radicals by an H-transfer reaction as can be followed by spectrophotometry. Besides radical transfer reactions β-fragmentation reactions occur causing chain scission. Such reactions can be followed in a pulse radiolysis experiment by conductometry, because counter ions are released upon chain scission. Such a process is especially effective in the case of polymethacrylic acid, where it results in a chain depolymerization. An intramolecular H-abstraction is also observed in the γ-radiolysis of polyacrylic acid with the corresponding peroxyl radicals. This causes a chain reaction to occur. The resulting hydroperoxides are unstable and decarboxylate given rise to acetylacetone-like products. In polyvinyl alcohol the peroxyl radicals in α-position to the alcohol function undergo HO2-elimination. This prevents a scission of the polymer chain in the

  14. Surface shape memory in polymers

    Science.gov (United States)

    Mather, Patrick

    2012-02-01

    Many crosslinked polymers exhibit a shape memory effect wherein a permanent shape can be prescribed during crosslinking and arbitrary temporary shapes may be set through network chain immobilization. Researchers have extensively investigated such shape memory polymers in bulk form (bars, films, foams), revealing a multitude of approaches. Applications abound for such materials and a significant fraction of the studies in this area concern application-specific characterization. Recently, we have turned our attention to surface shape memory in polymers as a means to miniaturization of the effect, largely motivated to study the interaction of biological cells with shape memory polymers. In this presentation, attention will be given to several approaches we have taken to prepare and study surface shape memory phenomenon. First, a reversible embossing study involving a glassy, crosslinked shape memory material will be presented. Here, the permanent shape was flat while the temporary state consisted of embossed parallel groves. Further the fixing mechanism was vitrification, with Tg adjusted to accommodate experiments with cells. We observed that the orientation and spreading of adherent cells could be triggered to change by the topographical switch from grooved to flat. Second, a functionally graded shape memory polymer will be presented, the grading being a variation in glass transition temperature in one direction along the length of films. Characterization of the shape fixing and recovery of such films utilized an indentation technique that, along with polarizing microscopy, allowed visualization of stress distribution in proximity to the indentations. Finally, very recent research concerning shape memory induced wrinkle formation on polymer surfaces will be presented. A transformation from smooth to wrinkled surfaces at physiological temperatures has been observed to have a dramatic effect on the behavior of adherent cells. A look to the future in research and

  15. Development of polymer packaging for power cable

    Directory of Open Access Journals (Sweden)

    S. Sremac

    2014-10-01

    Full Text Available This paper discusses the issues of product design and the procedure of developing polymer packaging as one of the most important engineering tasks. For the purpose of packing power cables a polymer packaging has been designed in the form of drum. Packaging and many other consumer products are largely produced using polymeric materials due to many positive features. High Density Polyethylene is the type of polyethylene proposed for packaging purposes due to its low degree of branching and strong intermolecular forces. Transport and storage processes were automated based on the radio-frequency identification technology. The proposed system is flexible in terms of its possibility of accepting and processing different types of cables and other products.

  16. Molecular and supramolecular orientation in conducting polymers

    International Nuclear Information System (INIS)

    Intrinsic anisotropy in electrical and optical properties of conducting polymers constitutes a unique aspect that derives π-electron delocalization along the polymer backbone and from the weak inter-chain interaction. To acquire such an intrinsic property, conducting polymers have to be oriented macroscopically and microscopically (at the chain level). A review of the various techniques, including stretch-alignment of the polymer and of precursor polymers, polymerization in ordered media, i.e., in a liquid crystal solvent, and synthesis of liquid crystalline conducting polymers will be given. 29 refs

  17. Method of Thermocleaving a Polymer Layer

    DEFF Research Database (Denmark)

    2010-01-01

    A method of thermocleaving a thermocleavable polymer layer which is in thermal contact with a heat sensitive component that is not tolerant of the temperature required for thermocleavage of the thermocleavable polymer layer, in which the thermocleavable polymer layer is illuminated with a light...... source having a wavelength range more strongly absorbed by the thermocleavable polymer and substantially less strongly absorbed by the heat sensitive component, such that the thermocleavable polymer layer reaches a temperature sufficient to cause thermocleavage of the polymer without causing detrimental...

  18. Polymers for energy storage and conversion

    CERN Document Server

    Mittal, Vikas

    2013-01-01

    One of the first comprehensive books to focus on the role of polymers in the burgeoning energy materials market Polymers are increasingly finding applications in the areas of energy storage and conversion. A number of recent advances in the control of the polymer molecular structure which allows the polymer properties to be more finely tuned have led to these advances and new applications. Polymers for Energy Storage and Conversion assimilates these advances in the form of a comprehensive text that includes the synthesis and properties of a large number of polymer systems for

  19. Editorial of the Special Issue Antimicrobial Polymers

    Directory of Open Access Journals (Sweden)

    Iolanda Francolini

    2013-09-01

    Full Text Available The special issue “Antimicrobial Polymers” includes research and review papers concerning the recent advances on preparation of antimicrobial polymers and their relevance to industrial settings and biomedical field. Antimicrobial polymers have recently emerged as promising candidates to fight microbial contamination onto surfaces thanks to their interesting properties. In this special issue, the main strategies pursued for developing antimicrobial polymers, including polymer impregnation with antimicrobial agents or synthesis of polymers bearing antimicrobial moieties, were discussed. The future application of these polymers either in industrial or healthcare settings could result in an extremely positive impact not only at the economic level but also for the improvement of quality of life.

  20. Cycloadditions in modern polymer chemistry.

    Science.gov (United States)

    Delaittre, Guillaume; Guimard, Nathalie K; Barner-Kowollik, Christopher

    2015-05-19

    Synthetic polymer chemistry has undergone two major developments in the last two decades. About 20 years ago, reversible-deactivation radical polymerization processes started to give access to a wide range of polymeric architectures made from an almost infinite reservoir of functional building blocks. A few years later, the concept of click chemistry revolutionized the way polymer chemists approached synthetic routes. Among the few reactions that could qualify as click, the copper-catalyzed azide-alkyne cycloaddition (CuAAC) initially stood out. Soon, many old and new reactions, including cycloadditions, would further enrich the synthetic macromolecular chemistry toolbox. Whether click or not, cycloadditions are in any case powerful tools for designing polymeric materials in a modular fashion, with a high level of functionality and, sometimes, responsiveness. Here, we wish to describe cycloaddition methodologies that have been reported in the last 10 years in the context of macromolecular engineering, with a focus on those developed in our laboratories. The overarching structure of this Account is based on the three most commonly encountered cycloaddition subclasses in organic and macromolecular chemistry: 1,3-dipolar cycloadditions, (hetero-)Diels-Alder cycloadditions ((H)DAC), and [2+2] cycloadditions. Our goal is to briefly describe the relevant reaction conditions, the advantages and disadvantages, and the realized polymer applications. Furthermore, the orthogonality of most of these reactions is highlighted because it has proven highly beneficial for generating unique, multifunctional polymers in a one-pot reaction. The overview on 1,3-dipolar cycloadditions is mostly centered on the application of CuAAC as the most travelled route, by far. Besides illustrating the capacity of CuAAC to generate complex polymeric architectures, alternative 1,3-dipolar cycloadditions operating without the need for a catalyst are described. In the area of (H)DA cycloadditions

  1. Solution assembly of conjugated polymers

    Science.gov (United States)

    Bokel, Felicia A.

    This dissertation focuses on the solution-state polymer assembly of conjugated polymers with specific attention to nano- and molecular-scale morphology. Understanding how to control these structures holds potential for applications in polymer-based electronics. Optimization of conjugated polymer morphology was performed with three objectives: 1) segregation of donor and acceptor materials on the nanometer length-scale, 2) achieving molecular-scale ordering in terms of crystallinity within distinct domains, and 3) maximizing the number and quality of well-defined donor/acceptor interfaces. Chapter 1 introduces the development of a mixed solvent method to create crystalline poly(3-hexyl thiophene) (P3HT) fibrils in solution. Chapter 2 describes fibril purification and approaches to robust and functional fibrils, while chapters 3 and 4 demonstrate the formation of hybrid nanocomposite wires of P3HT and cadmium selenide (CdSe) nanoparticles by two methods: 1) co-crystallization of free and P3HT-grafted CdSe for composite nanowires and 2) direct attachment of CdSe nanoparticles at fibril edges to give superhighway structures. These composite structures show great potential in the application of optoelectronic devices, such as the active layer of solar cells. Finally, ultrafast photophysical characterization of these polymers, using time-resolved photoluminescence and transient absorption, was performed to determine the aggregation types present in suspended fibrils and monitor the formation and decay of charged species in fibrils and donor-acceptor systems.

  2. Ring polymers in confined geometries

    CERN Document Server

    Usatenko, Z; Kuterba, P

    2016-01-01

    The investigation of a dilute solution of phantom ideal ring polymers and ring polymers with excluded volume interactions (EVI) in a good solvent confined in a slit geometry of two parallel repulsive walls and in a solution of colloidal particles of big size were performed. Taking into account the correspondence between the field theoretical $\\phi^4$ $O(n)$-vector model in the limit $n\\to 0$ and the behavior of long-flexible polymer chains in a good solvent the correspondent depletion interaction potentials, depletion forces and the forces which exert phantom ideal ring and ring polymer chains with EVI on the walls were obtained in the framework of the massive field theory approach at fixed space dimensions d=3 up to one-loop order. Additionally, the investigation of a dilute solution of phantom ideal ring polymers in a slit geometry of two inert walls and mixed walls with one repulsive and other one inert wall were performed and correspondent depletion interaction potentials and the depletion forces were cal...

  3. Green Polymer Chemistry: Enzyme Catalysis for Polymer Functionalization

    Directory of Open Access Journals (Sweden)

    Sanghamitra Sen

    2015-05-01

    Full Text Available Enzyme catalyzed reactions are green alternative approaches to functionalize polymers compared to conventional methods. This technique is especially advantageous due to the high selectivity, high efficiency, milder reaction conditions, and recyclability of enzymes. Selected reactions can be conducted under solventless conditions without the application of metal catalysts. Hence this process is becoming more recognized in the arena of biomedical applications, as the toxicity created by solvents and metal catalyst residues can be completely avoided. In this review we will discuss fundamental aspects of chemical reactions biocatalyzed by Candida antarctica lipase B, and their application to create new functionalized polymers, including the regio- and chemoselectivity of the reactions.

  4. Green polymer chemistry: enzyme catalysis for polymer functionalization.

    Science.gov (United States)

    Sen, Sanghamitra; Puskas, Judit E

    2015-05-21

    Enzyme catalyzed reactions are green alternative approaches to functionalize polymers compared to conventional methods. This technique is especially advantageous due to the high selectivity, high efficiency, milder reaction conditions, and recyclability of enzymes. Selected reactions can be conducted under solventless conditions without the application of metal catalysts. Hence this process is becoming more recognized in the arena of biomedical applications, as the toxicity created by solvents and metal catalyst residues can be completely avoided. In this review we will discuss fundamental aspects of chemical reactions biocatalyzed by Candida antarctica lipase B, and their application to create new functionalized polymers, including the regio- and chemoselectivity of the reactions.

  5. High performance polymer concrete

    Directory of Open Access Journals (Sweden)

    Frías, M.

    2007-06-01

    Full Text Available This paper studies the performance of concrete whose chief components are natural aggregate and an organic binder —a thermosetting polyester resin— denominated polymer concrete or PC. The material was examined macro- and microscopically and its basic physical and mechanical properties were determined using mercury porosimetry, scanning electron microscopy (SEM-EDAX, X-ray diffraction (XRD and strength tests (modulus of elasticity, stress-strain curves and ultimate strengths. According to the results of these experimental studies, the PC exhibited a low density (4.8%, closed pore system and a concomitantly continuous internal microstructure. This would at least partially explain its mechanical out-performance of traditional concrete, with average compressive and flexural strength values of 100 MPa and over 20 MPa, respectively. In the absence of standard criteria, the bending test was found to be a useful supplement to compressive strength tests for establishing PC strength classes.Este trabajo de investigación aborda el estudio de un hormigón de altas prestaciones, formado por áridos naturales y un aglomerante orgánico constituido por una resina termoestable poliéster, denominado hormigón polimérico HP. Se describe el material a nivel microscópico y macroscópico, presentando sus propiedades físicas y mecánicas fundamentales, mediante diferentes técnicas experimentales, tales como: porosimetría de mercurio, microscopía electrónica (SEM-EDAX, difracción de rayos X (DRX y ensayos mecánicos (módulo de elasticidad, curvas tensión- deformación y resistencias últimas. Como consecuencia del estudio experimental llevado a cabo, se ha podido apreciar cómo el HP está formado por porosidad cerrada del 4,8%, proporcionando una elevada continuidad a su microestructura interna, lo que justifica, en parte, la mejora de propiedades mecánicas respecto al hormigón tradicional, con unos valores medios de resistencia a compresión de 100

  6. Photoconductive properties of conjugated polymers

    CERN Document Server

    Halls, J J M

    1997-01-01

    The research described in my dissertation has involved the fabrication and characterisation of photovoltaic cells based on conjugated polymers, including the widely studied polymer poly(p-phenylenevinylene). These materials have semiconducting properties which arise from the delocalisation of electrons along the pi-electron systems of the polymer chains. Research into these materials is motivated both by their novel electronic properties, and also their potential for use in a wide range of applications including light-emitting diodes (LEDs), thin-film transistors, and photovoltaic cells (solar cells and light detectors). Light absorbed in a photovoltaic cell generates opposite charges which are collected at two different electrodes, giving rise to an electric current

  7. Polyamide 6 single polymer composites

    Directory of Open Access Journals (Sweden)

    2009-08-01

    Full Text Available Combining the two basic techniques used for the preparation of single polymer composites (SPCs, hot compaction and film stacking, a polyamide 6 (PA 6 single polymer composite was manufactured. The starting materials were PA 6 high tenacity yarn (reinforcement and PA 6 film prepared via melt quenching (matrix, both expected to be the two principal polymorphic modifications of PA 6 and thus differing in their melting temperatures. The prepared single polymer composite is characterized by a layered structure and shows superior mechanical properties due to the good wetting – tensile modulus is improved by 200% and the ultimate tensile strength – by 300–400% as compared to the isotropic matrix film. Improvement of the interfacial adhesion via transreactions promoted by Sb2O3 as a catalyst was also undertaken.

  8. Water Soluble Responsive Polymer Brushes

    Directory of Open Access Journals (Sweden)

    Andrew J. Parnell

    2011-12-01

    Full Text Available Responsive polymer brushes possess many interesting properties that enable them to control a range of important interfacial behaviours, including adhesion, wettability, surface adsorption, friction, flow and motility. The ability to design a macromolecular response to a wide variety of external stimuli makes polymer brushes an exciting class of functional materials, and has been made possible by advances in modern controlled polymerization techniques. In this review we discuss the physics of polymer brush response along with a summary of the techniques used in their synthesis. We then review the various stimuli that can be used to switch brush conformation; temperature, solvent quality, pH and ionic strength as well as the relatively new area of electric field actuation We discuss examples of devices that utilise brush conformational change, before highlighting other potential applications of responsive brushes in real world devices.

  9. Green polymer chemistry: Synthesis of poly(disulfide) polymers and networks

    Science.gov (United States)

    Rosenthal-Kim, Emily Quinn

    distribution of around 1.15. However, the majority of the product consists of low molecular weight cyclic poly(disulfide) oligomers. In reactions maintained below 18°C, the organic components were miscible in the aqueous hydrogen peroxide and a milky emulsion was produced. The polymers were degraded using the disulfide-specific reducing agent, dithiothreitol. Poly(disulfide) polymer networks were also synthesized in a two-phase system. Due to the poor solubility of the crosslinker, trimethylolpropane tris(2-mercaptopropionate, organic solvents were required to obtain consistent networks. The networks were degraded using dithiothreitol in tetrahydrofuran. The networks were stable under aqueous reducing conditions. The disulfide-bearing biochemical, alpha-lipoic acid, was investigated as monomer for the new method of poly(disulfide) polymer synthesis. It was also polymerized thermally and by a new interfacial method that proceeds at the air-water interface. Polymer products were often too large to be characterized by SEC (Mn > 1,000,000 g/mol). A poly(alpha-LA) polymer sample showed mass loss in aqueous solutions of glutathione at pH = 5.2 which was used to model cytosolic conditions. Poly(alpha-LA) was decorated with PEG (2,000 g/mol) in an esterification reaction catalyzed by Candida antarctica lipase B (CALB). The decorated polymers were imaged using AFM which revealed branch-like structures. To make new alpha-lipoic acid based monomers and macromonomers, CALB-catalyzed esterification, was used to conjugate alpha-lipoic acid to a variety of glycols including: diethylene glycol monomethyl ether, tetraethylene glycol, hexaethylene glycol, and poly(ethylene glycol). The products were verified using NMR spectroscopy and mass spectrometry.

  10. HIGH TEMPERATURE POLYMER FUEL CELLS

    DEFF Research Database (Denmark)

    Jensen, Jens Oluf; Qingfeng, Li; He, Ronghuan;

    2003-01-01

    This paper will report recent results from our group on polymer fuel cells (PEMFC) based on the temperature resistant polymer polybenzimidazole (PBI), which allow working temperatures up to 200°C. The membrane has a water drag number near zero and need no water management at all. The high working...... temperature allows for utilization of the excess heat for fuel processing. Moreover, it provides an excellent CO tolerance of several percent, and the system needs no purification of hydrogen from a reformer. Continuous service for over 6 months at 150°C has been demonstrated....

  11. Polymer photovoltaics a practical approach

    CERN Document Server

    Krebs, Frederik C

    2008-01-01

    This book is intended to be a practical guide in the laboratory for the experimental solar-cell scientist whether he or she is involved with synthesis, device preparation, processing, or device characterization. Useful to all scientists working practically in the field, the book presents the process of creating a polymer solar-cell device beginning with a description of materials, including how they are made and characterized, followed by how the materials are processed into devices and films, and how these are characterized. From there, the status of two emerging fields of polymer solar cells

  12. Australian polymer banknote: a review

    Science.gov (United States)

    Wilson, Gerard J.

    1998-04-01

    In 1996 Australia became the first country in the world to have an all-polymer currency in general circulation. Australia's first polymer note was a commemorative note that was issued in January 1988 to celebrate the bicentenary of European settlement. That note was the culmination of almost twenty year's collaboration between the Reserve Bank of Australia and the Commonwealth Scientific and Industrial Research Organisation. This paper traces the development of the Bicentennial Banknote note from its conception at a brain- storming meeting between RBA and CSIRO scientists in 1968 through to its release in 1988.

  13. Mass Spectrometry in Polymer Chemistry

    CERN Document Server

    Barner-Kowollik, Christopher; Falkenhagen, Jana; Weidner, Steffen

    2011-01-01

    Combining an up-to-date insight into mass-spectrometric polymer analysis beyond MALDI with application details of the instrumentation, this is a balanced and thorough presentation of the most important and widely used mass-spectrometric methods.Written by the world's most proficient experts in the field, the book focuses on the latest developments, covering such technologies and applications as ionization protocols, tandem and liquid chromatography mass spectrometry, gas-phase ion-separation techniques and automated data processing. Chapters on sample preparation, polymer degradation and the u

  14. Liquid crystalline order in polymers

    CERN Document Server

    Blumstein, Alexandre

    1978-01-01

    Liquid Crystalline Order in Polymers examines the topic of liquid crystalline order in systems containing rigid synthetic macromolecular chains. Each chapter of the book provides a review of one important area of the field. Chapter 1 discusses scattering in polymer systems with liquid crystalline order. It also introduces the field of liquid crystals. Chapter 2 treats the origin of liquid crystalline order in macromolecules by describing the in-depth study of conformation of such macromolecules in their unassociated state. The chapters that follow describe successively the liquid crystalli

  15. Polymer electronics a flexible technology

    CERN Document Server

    Technology, Rapra

    2009-01-01

    The worldwide market for polymer electronic products has been estimated to be worth up to £15 billion by 2015 and the opportunity for new markets could be as high as £125 billion by 2025.'The rapid development of polymer electronics has revealed the possibility for transforming the electronics market by offering lighter, flexible and more cost effective alternatives to conventional materials and products. With applications ranging from printed, flexible conductors and novel semiconductor components to intelligent labels and large area displays and solar panels, products that were previously un

  16. Characterization of Reillex HPQ Polymer

    International Nuclear Information System (INIS)

    This work examined the thermal stability of Reillex(tm) HPQ resin as part of a comprehensive plan to qualify that material for use in HB-line. No low temperature exothermic reactions or volatile organic compounds occurred in various lots of as-received, chloride form Reillex(tm) HPQ polymer or the nitrate form polymer. The studies do not suggest any restrictions on purchase criteria for the resin nor any changes in planned use. Previously observed low temperature exotherms resulted from reaction of nitric acid with the aluminum sample holders used in the Differential Scanning Calorimetry analysis

  17. Polymer Structure--Organic Aspects (Definitions).

    Science.gov (United States)

    Carraher, Charles E., Jr.; Seymour, Raymond B.

    1988-01-01

    Lists alphabetically the definitions of key organic-based terms used in characterizing the structure of polymers. Includes several common polymers, some of their uses and their respective structures. (CW)

  18. The Research of Biomedical Intelligent Polymer Materials

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zhi-bin; CHEN Yuan-wei; TANG Chang-wei; QIU Kai; LUO Juan; XU Cheng-yin; WAN Chang-xiu

    2004-01-01

    The properties of biomedical intelligent polymer materials can be changed obviously when there is a little physical or chemical change caused by external condition. They are in the forms of solids, solutions and the polymers on the surface of carrier, and include water solution of hydrophilic polymers, cross-linking hydrophilic polymers(i.e. hydrogels) and the polymers on the surface of carrier. The environmental stimulating factors are temperature, pH value, composition of solution, ionic intention, light intention, electric field, stress field and magnetic field etc.. The properties of intelligent polymer are those of phase, photics, mechanics, electric field, surface energy,reaction ratio, penetrating ratio and recognition etc..Stimulation-response of intelligent water-soluble polymerWater-soluble intelligent polymer can be separated out from solution under special external condition. It can be used as the switch of temperature or pH indicator. When water-soluble intelligent polymer is mixed with soluble-enzyme matter or cell suspension, the polymer can bring phase separation and react with soluble-enzyme matter or cell membrane through accepting some external stimulation. Other water-soluble intelligent polymer is that can make the main chemical group of some natural biomolecular recognition sequence section to arrange on skeleton of polymer at random. It is the same ratio as natural biomolecules.Stimulation-response of intelligent polymer of carrier surface Intelligent polymer can be fixed on the surface of solid polymer carrier through chemical grafting or physical adsorption. When the external conditions are changed, the thickness, humidity and electric field of the surface layer will be changed. Intelligent polymer can be preparated the permanence switch by precipitating into the hole of porous surface, and it can control on-off state of the hole. When protein or cell interacts with intelligent polymer surface to be placed in to open or close, they can be

  19. Polymer Electrolytes for Lithium/Sulfur Batteries

    Directory of Open Access Journals (Sweden)

    The Nam Long Doan

    2012-08-01

    Full Text Available This review evaluates the characteristics and advantages of employing polymer electrolytes in lithium/sulfur (Li/S batteries. The main highlights of this study constitute detailed information on the advanced developments for solid polymer electrolytes and gel polymer electrolytes, used in the lithium/sulfur battery. This includes an in-depth analysis conducted on the preparation and electrochemical characteristics of the Li/S batteries based on these polymer electrolytes.

  20. Polymers used in papermaking industry process

    OpenAIRE

    Guo, Rui; Wang, Yang

    2014-01-01

    This thesis is accomplished in Tampere University of Applied Sciences. Polymers used in paper making process are discussed in this thesis. This thesis is divided into two parts. One part lists polymers applied in different sections on a paper machine. Another part is about polymers in paper grades. Mainly used polymers in papermaking industry process are listed below: Polyethylene, known as PE, is used in extrusion coating and lamination. Products like film, packaging bags, containers ...

  1. Photodegradation of polymers physical characteristics and applications

    CERN Document Server

    Rabek, Jan F

    1996-01-01

    In this book on physical characteristics and practical aspects of polymer photodegradation Rabek emphasizes the experimental work on the subject. The most important feature of the book is the physical interpretation of polymer degradation, e.g. mechanism of UV/light absorption, formation of excited states, energy transfer mechanism, kinetics, dependence on physical properties of macromolecules and polymer matrices, formation of mechanical defects, practics during environmental ageing. He includes also some aspects of polymer photodegradation in environmental and space condition.

  2. Recent developments in high temperature organic polymers

    Science.gov (United States)

    Hergenrother, P. M.

    1991-01-01

    Developments in high temperature organic polymers during the last 5 years with major emphasis on polyimides and poly(arylene ether)s are discussed. Specific polymers or series of polymers have been selected to demonstrate unique properties or the effect chemical structure has upon certain properties. This article is not intended to be a comprehensive review of high temperature polymer advancements during the last 5 years.

  3. Interfacial Slip in Sheared Polymer Blends

    OpenAIRE

    Lo, Tak Shing; Mihajlovic, Maja; Shnidman, Yitzhak; Li, Wentao; Gersappe, Dilip

    2004-01-01

    We have developed a dynamic self-consistent field theory, without any adjustable parameters, for unentangled polymer blends under shear. Our model accounts for the interaction between polymers, and enables one to compute the evolution of the local rheology, microstructure and the conformations of the polymer chains under shear self-consistently. We use this model to study the interfacial dynamics in sheared polymer blends and make a quantitative comparison between this model and Molecular Dyn...

  4. Solventless processing of conjugated polymers - a review

    OpenAIRE

    Brandão, Lúcia; Viana, Júlio; David G. Bucknall; Bernardo, Gabriel

    2014-01-01

    The molecular mobility of polymers in their solid or molten states allows their processing without the need for toxic, “non-friendly” solvents. In this work, the main features of solvent-free processing methods applied to conjugated polymers are reviewed taking into consideration that these materials are largely used in a broad range of (opto-)electronic applications, including organic field-effect transistors, polymer light-emitting diodes and polymer photovoltaic devices. This review addres...

  5. Kinetics of polymer adsorption, desorption and exchange.

    NARCIS (Netherlands)

    Dijt, J.C.

    1993-01-01

    The aim of the study in this thesis was to gain more insight in the kinetics of polymer adsorption. To this end some well-characterised polymers have been systematically investigated.In the process of polymer adsorption one may distinguish three kinetic contributions: transport to the surface, attac

  6. Polymer flexibility and turbulent drag reduction.

    Science.gov (United States)

    Gillissen, J J J

    2008-10-01

    Polymer-induced drag reduction is the phenomenon by which the friction factor of a turbulent flow is reduced by the addition of small amounts of high-molecular-weight linear polymers, which conformation in solution at rest can vary between randomly coiled and rodlike. It is well known that drag reduction is positively correlated to viscous stresses, which are generated by extended polymers. Rodlike polymers always assume this favorable conformation, while randomly coiling chains need to be unraveled by fluid strain rate in order to become effective. The coiling and stretching of flexible polymers in turbulent flow produce an additional elastic component in the polymer stress. The effect of the elastic stresses on drag reduction is unclear. To study this issue, we compare direct numerical simulations of turbulent drag reduction in channel flow using constitutive equations describing solutions of rigid and flexible polymers. When compared at constant phi r2, both simulations predict the same amount of drag reduction. Here phi is the polymer volume fraction and r is the polymer aspect ratio, which for flexible polymers is based on average polymer extension at the channel wall. This demonstrates that polymer elasticity plays a marginal role in the mechanism for drag reduction.

  7. Green polymer chemistry: biocatalysis and biomaterials

    Science.gov (United States)

    This overview briefly surveys the practice of green chemistry in polymer science. Eight related themes can be discerned from the current research activities: 1) biocatalysis, 2) bio-based building blocks and agricultural products, 3) degradable polymers, 4) recycling of polymer products and catalys...

  8. Challenges in polymer analysis by liquid chromatography

    NARCIS (Netherlands)

    E. Uliyanchenko; S. van der Wal; P.J. Schoenmakers

    2012-01-01

    Synthetic polymers are very important in our daily life. Many valuable properties of polymers are determined by their molecular weight and chemical composition. Liquid chromatographic (LC) techniques are very commonly used for molecular characterisation of polymers. LC analysis of macromolecules is

  9. Education: Firms Offer Academics Polymer Science Training.

    Science.gov (United States)

    Chemical and Engineering News, 1983

    1983-01-01

    Provides information on industry-sponsored programs for college faculty and advanced undergraduate students designed to improve polymer science training: these include residency programs for professors available at industrial laboratories, establishment of a Polymer Education Award, newsletter on course materials/sources in polymer science,…

  10. Polymer Chemistry: Introduction to an Indispensable Science

    Science.gov (United States)

    Teegarden, David M.

    2004-01-01

    More than half of all chemists work on some aspect of polymers. For high school teachers who want to introduce polymer science basics, properties, and uses, this book is uniquely helpful--much deeper than simple monographs or collections of experiments, but much more accessible than college texts. Divided into four sections, Polymer Chemistry…

  11. 21 CFR 177.1420 - Isobutylene polymers.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Isobutylene polymers. 177.1420 Section 177.1420... FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1420 Isobutylene polymers....

  12. Advancement in polymer therapeutics and characterization

    Directory of Open Access Journals (Sweden)

    Shah Pratik

    2009-01-01

    Full Text Available The beauty of the discipline, polymers in drug delivery, is its longevity and self-transforming quality. Polymers have, for decades, performed a valuable function as excipients in tablet and capsule formulations, moving steadily into the parenteral arena as blood circulation time enhancers, and are now capable of offering advanced and sophisticated functions (such as drug targeting to medicine. Polymers have unique cooperative properties that are not found with low-molecular weight compounds and therein lies the root of their success. Polymers are used as carriers for the delivery of drugs, proteins, targeting moieties, and imaging agents. Several polymers, polyethylene glycol, N-(2-hydroxypropyl methacrylamide, and polylactide-co-glycolidecopolymers have been successfully utilized in clinical research. Recently, interest in polymer conjugation with biologically active components has increased remarkably as such conjugates are preferably accumulated in solid tumors and can reduce systemic toxicity. Further, it is essential to elucidate the structure-activity relationshipof a drug when it is conjugated with a polymer using different conjugation sites as this can vary the efficacy and mechanism of action when compared with its free form. This review will discuss the current advancement in drug targeting with polymers, smart polymers and recombinant polymers for drug delivery. Finally, it will also highlight on various methods of polymer characterization, including various techniques for polymer molecular weight measurement.

  13. SYNTHESES AND PROPERTIES OF SOME ORGANOSILANE POLYMERS

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xinghua; Robert West

    1984-01-01

    Some organosilane polymers with high molecular weights have been synthesized by cocondensation of organosilicon dihalide monomers with sodium metal in toluene. These polymers are both soluble in common solvents and meltable at lower temperatures, and can be molded, cast into films or drawn into fibers. Exposure of the solid polymers to ultraviolet light leads to degradation or crosslinking.

  14. Polymer constraint effect for electrothermal bimorph microactuators

    NARCIS (Netherlands)

    Chu Duc, T.; Lau, G.K.; Sarro, P.M.

    2007-01-01

    The authors report on the analysis of the polymer constraint effect and its use for a micromachined electrothermal bimorph actuator. The actuated displacement is enhanced due to the polymer constraint effect. Both the thermal expansion and apparent Young’s modulus of the constrained polymer blocks a

  15. 40 CFR 721.8090 - Polyurethane polymer.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polyurethane polymer. 721.8090 Section... Substances § 721.8090 Polyurethane polymer. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a polyurethane polymer (P-94-47) is...

  16. Integration of active and passive polymer optics

    DEFF Research Database (Denmark)

    Christiansen, Mads Brøkner; Schøler, Mikkel; Kristensen, Anders

    2007-01-01

    We demonstrate a wafer scale fabrication process for integration of active and passive polymer optics: Polymer DFB lasers and waveguides. Polymer dye DFB lasers are fabricated by combined nanoimprint and photolithography (CNP). The CNP fabrication relies on an UV transparent stamp with nm sized...

  17. A merocyanine-based conductive polymer

    OpenAIRE

    Wagner, Klaudia; Zanoni, Michele; Elliott, Anastasia B. S.; Wagner, Pawel; Byrne, Robert; Florea, Larisa; Diamond, Dermot; Gordon, Keith; Wallace, Gordon; Officer, David

    2013-01-01

    We report the first example of a conducting polymer with a merocyanine incorporated into the polymer backbone by electropolymerisation of a spiropyran moiety covalently linked between two alkoxythiophene units. Utilising the known metal coordination capabilities of merocyanines, introduction of cobalt ions into the electropolymerisation led to an enhancement of the conductivity, morphology and optical properties of the polymer films.

  18. Electrically conducting polymers for aerospace applications

    Science.gov (United States)

    Meador, Mary Ann B.; Gaier, James R.; Good, Brian S.; Sharp, G. R.; Meador, Michael A.

    1991-01-01

    Current research on electrically conducting polymers from 1974 to the present is reviewed focusing on the development of materials for aeronautic and space applications. Problems discussed include extended pi-systems, pyrolytic polymers, charge-transfer systems, conductive matrix resins for composite materials, and prospects for the use of conducting polymers in space photovoltaics.

  19. Triphenylamine-based amorphous polymers for bulk-heterojunction photovoltaic cells

    International Nuclear Information System (INIS)

    In this paper, the recent research progress on triphenylamine (TPA)-based donor-acceptor (D-A) amorphous polymers including our developed polymers is reviewed. TPA has three-dimensional branched structures and can provide D-A polymers containing D and A units in the main chain or side chain. The use of TPA-based amorphous polymers in the fabrication of organic photovoltaics (OPVs) offers great advantages over the use of a polycrystalline film in terms of high reproducibility of the OPV performance. The amorphous polymer design using TPA, therefore, indicates a promising direction for the development of new donor materials in OPVs

  20. Large and Reversible Plasmon Tuning using Ultrathin Responsive Polymer film

    Science.gov (United States)

    Singamaneni, Srikanth; Nergiz, Saide

    2011-03-01

    We demonstrate reversible linear and branched aggregation of gold nanoparticles adsorbed on an ultrathin responsive polymer ((poly(4-vinyl pyridine), P4VP) film. P4VP is a weak cationic polymer, which exhibits a reversible coil to globule transition with change in external pH. Atomic force microscopy revealed that in the coiled state (below the isoelectric point of the polymer) of the polymer chains, gold nanoparticles adsorbed on the polymer layer existed as primarily individual nanoparticles. On the other hand, lowering the pH caused the polymer chains to transition from coil to globule state, resulting in aggregation of the nanoparticles into linear and branched chains. Reversible aggregation of the nanoparticles results in a dramatic change in the optical properties of the metal nanostructures. Apart from the large redistribution of the intensity between the individual (530 nm) and coupled (650 nm) plasmon bands, the coupled plasmon band exhibits a shift of nearly 60 nm with change in external pH. The pH triggered aggregation of the nanoparticles and the dramatic change in the optical properties associated with the same can form an excellent platform for colorimetric sensing. The work reported here is supported by the Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine.

  1. Mechanical properties and morphology of polymer gels

    Science.gov (United States)

    Sliozberg, Yelena; Sirk, Timothy; Brennan, John; Andzelm, Jan; Mrozek, Randy; Lenhart, Joseph

    2012-02-01

    Understanding morphology and mechanical response of polymeric gels is of particular importance to design materials with required energy dissipation characteristics. We will present our latest results for polymer gels based on 1) self-assembled block copolymers and 2) chemically cross-linked polymers. The dissipative particle dynamics (DPD) was used to predict morphology in good agreement with atomic force microscopy. We have performed DPD non-equilibrium oscillatory shear calculations predicting elastic modulus of unentangled gels that correlates well with experimental rheology data. However, this methodology fails to predict mechanics of entangled polymer networks due to unphysical chain crossing brought by the soft potentials used in DPD simulations. Recently, we have introduced an improved segmental repulsion potential that removes the bond crossing allowing for reptation dynamics. The improved DPD method was used in simulations for entangled gels to explore impact of branched architecture of solvent on the mechanical response to the tensile deformation. Novel architectures of solvent resulting in a dramatic increase of the elastic modulus were identified. The topological analysis was applied to understand contributions of chemical cross-links and entanglements to the stress.

  2. Polymer therapeutics in surgery: the next frontier

    Science.gov (United States)

    Conlan, R. Steven; Whitaker, Iain S.

    2016-01-01

    Abstract Polymer therapeutics is a successful branch of nanomedicine, which is now established in several facets of everyday practice. However, to our knowledge, no literature regarding the application of the underpinning principles, general safety, and potential of this versatile class to the perioperative patient has been published. This study provides an overview of polymer therapeutics applied to clinical surgery, including the evolution of this demand‐oriented scientific field, cutting‐edge concepts, its implications, and limitations, illustrated by products already in clinical use and promising ones in development. In particular, the effect of design of polymer therapeutics on biophysical and biochemical properties, the potential for targeted delivery, smart release, and safety are addressed. Emphasis is made on principles, giving examples in salient areas of demand in current surgical practice. Exposure of the practising surgeon to this versatile class is crucial to evaluate and maximise the benefits that this established field presents and to attract a new generation of clinician–scientists with the necessary knowledge mix to drive highly successful innovation. PMID:27588210

  3. Encapsulation of polymer photovoltaic prototypes

    DEFF Research Database (Denmark)

    Krebs, Frederik C

    2006-01-01

    A simple and efficient method for the encapsulation of polymer and organic photovoltaic prototypes is presented. The method employs device preparation on glass substrates with subsequent sealing using glass fiber reinforced thermosetting epoxy (prepreg) against a back plate. The method allows...

  4. Polymer Chemistry and Liposome Technology

    OpenAIRE

    Tirrell, David A.

    1988-01-01

    Polymer chemistry has a great deal to offer in the construction of synthetic liposomal membranes for use in biology and medicine. This chapter explores the preparation and properties of polymeric liposomes , with particular emphasis on the use of controlled polyelectrolyte adsorption to manipulate liposomal membrane properties.

  5. An introduction to polymer nanocomposites

    International Nuclear Information System (INIS)

    This review presents an overview of the formulation, characterization and range of applications for polymer nanocomposites. After explaining how material properties at the nanometre scale can vary compared to those observed at longer length scales, typical methods used to formulate and characterize nanocomposites at laboratory and industrial scale will be described. The range of mechanical, electrical and thermal properties obtainable from nanocomposite materials, with examples of current commercial applications, will be outlined. Formulation and characterization of nanoparticle, nanotube and graphene composites will be discussed by reference to nanoclay-based composites, as the latter are presently of most technological relevance. Three brief case studies are presented to demonstrate how structure/property relationships may be controlled in a variety of polymer nanocomposite systems to achieve required performance in a given application. The review will conclude by discussing potential obstacles to commercial uptake of polymer nanocomposites, such as inconsistent protocols to characterize nanocomposites, cost/performance balances, raw material availability, and emerging legislation, and will conclude by discussing the outlook for future development and commercial uptake of polymer nanocomposites. (review)

  6. INFRARED EMISSIVITY OF CONDUCTING POLYMERS

    Institute of Scientific and Technical Information of China (English)

    WAN Meixiang; LI Suzhen; LI Junchao; DONG Haiou

    1991-01-01

    The infrared emissivity of conducting polymers in 8-20μm and at 50-150℃ in the direction of normal line has been measured as a function of wavelength, conductivity at room temperature,counterion, doping levels, measuring temperature and thickness of sample.

  7. Cell microencapsulation with synthetic polymers.

    Science.gov (United States)

    Olabisi, Ronke M

    2015-02-01

    The encapsulation of cells into polymeric microspheres or microcapsules has permitted the transplantation of cells into human and animal subjects without the need for immunosuppressants. Cell-based therapies use donor cells to provide sustained release of a therapeutic product, such as insulin, and have shown promise in treating a variety of diseases. Immunoisolation of these cells via microencapsulation is a hotly investigated field, and the preferred material of choice has been alginate, a natural polymer derived from seaweed due to its gelling conditions. Although many natural polymers tend to gel in conditions favorable to mammalian cell encapsulation, there remain challenges such as batch to batch variability and residual components from the original source that can lead to an immune response when implanted into a recipient. Synthetic materials have the potential to avoid these issues; however, historically they have required harsh polymerization conditions that are not favorable to mammalian cells. As research into microencapsulation grows, more investigators are exploring methods to microencapsulate cells into synthetic polymers. This review describes a variety of synthetic polymers used to microencapsulate cells. PMID:24771675

  8. Water-soluble conductive polymers

    Science.gov (United States)

    Aldissi, Mahmoud

    1989-01-01

    Polymers which are soluble in water and are electrically conductive. The monomer repeat unit is a thiophene or pyrrole molecule having an alkyl group substituted for the hydrogen atom located in the beta position of the thiophene or pyrrole ring and having a surfactant molecule at the end of the alkyl chain. Polymers of this class having 8 or more carbon atoms in the alkyl chain exhibit liquid crystalline behavior, resulting in high electrical anisotropy. The monomer-to-monomer bonds are located between the carbon atoms which are adjacent to the sulfur or nitrogen atoms. The number of carbon atoms in the alkyl group may vary from 1 to 20 carbon atoms. The surfactant molecule consists of a sulfonate group, or a sulfate group, or a carboxylate group, and hydrogen or an alkali metal. Negative ions from a supporting electrolyte which may be used in the electrochemical synthesis of a polymer may be incorporated into the polymer during the synthesis and serve as a dopant to increase the conductivity.

  9. Multilayer polymer light emitting devices

    Science.gov (United States)

    Barcikowski, Zachary; Thomas, Adam; Tzolov, Marian

    2013-03-01

    The interplay of device layers and their interfaces is a major area of study in Polymer Light Emitting Devices (PLEDs). Many factors such as the degradation, efficiency, and overall performance depend on how these layers interact with each other. A fundamental understanding of the interfaces of these layers can lend to better performing devices using a multitude of organic polymers deposited in conjunction with each other in several ways. We have studied basic PLED devices in which we vary the emissive layer used, along with final bake temperatures. Devices include a glass substrate with Indium Tin Oxide anode, Aluminum cathode, and Plexcore Hole Injection layer. The active polymer films were spin casted from solution of MEH-PPV and PFO. Single layer and dual layers of several polymers are studied by examining current-voltage characteristics, film densities, impedance measurements, light emission, and efficiency calculations. We have found that not only do dual layers positively alter the performance of the device in the majority of cases, but the solvents in which each layer is originally in when deposited affects the formation of the interface, thereby altering the device mechanisms.

  10. Persistence length of dendronized polymers

    NARCIS (Netherlands)

    Mikhailov, I.V.; Darinskii, A.A.; Zhulina, E.B.; Borisov, O.V.; Leermakers, F.A.M.

    2015-01-01

    We present numerical results for the thermodynamic rigidity and induced persistence length of dendronized polymers with systematically varied topology of their grafts obtained by the Scheutjens-Fleer self-consistent field method. The results were compared to predictions of an analytical mean-fiel

  11. Responsive Polymers for Crop Protection

    Directory of Open Access Journals (Sweden)

    Serban F. Peteu

    2010-08-01

    Full Text Available This review outlines the responsive polymer methods currently in use with their potential application to plant protection and puts forward plant-specific mechanisms as stimuli in newly devised methods for smart release of crop protection agents (CPAs. CPAs include chemicals (fungicides, insecticides, herbicides, biochemicals (antibiotics, RNA-based vaccines for plant viruses, semiochemicals (pheromones, repellents, allomones, microbial pesticides, growth regulators (insect and plant or micronutrients, all with crop protection effects. This appraisal focuses on emerging uses of polymer nano-encapsulated CPAs. Firstly, the most interesting advances in controlled release methods are critically discussed with their advantages and drawbacks. Secondly, several plant-specific stimuli-based smart methods are anticipated for use alongside the polymer nano- or micro-capsules. These new CPA release methods are designed to (i protect plants against infection produced by fungi or bacteria, and (ii apply micro-nutrients when the plants need it the most. Thus, we foresee (i the responsive release of nano- encapsulated bio-insecticides regulated by plant stress enzymes, and (ii the delivery of micro-nutrients synchronized by the nature or intensity of plant root exudates. Such continued advances of nano-scale smart polymer-based CPAs for the protection of crops herald a “small revolution” for the benefit of sustainable agriculture.

  12. Controlled Release from Recombinant Polymers

    OpenAIRE

    Price, Robert; Poursaid, Azadeh; Ghandehari, Hamidreza

    2014-01-01

    Recombinant polymers provide a high degree of molecular definition for correlating structure with function in controlled release. The wide array of amino acids available as building blocks for these materials lend many advantages including biorecognition, biodegradability, potential biocompatibility, and control over mechanical properties among other attributes. Genetic engineering and DNA manipulation techniques enable the optimization of structure for precise control over spatial and tempor...

  13. Subgap Absorption in Conjugated Polymers

    Science.gov (United States)

    Sinclair, M.; Seager, C. H.; McBranch, D.; Heeger, A. J; Baker, G. L.

    1991-01-01

    Along with X{sup (3)}, the magnitude of the optical absorption in the transparent window below the principal absorption edge is an important parameter which will ultimately determine the utility of conjugated polymers in active integrated optical devices. With an absorptance sensitivity of conjugated polymers poly(1,4-phenylene-vinylene) (and derivitives) and polydiacetylene-4BCMU in the spectral region from 0.55 eV to 3 eV. Our spectra show that the shape of the absorption edge varies considerably from polymer to polymer, with polydiacetylene-4BCMU having the steepest absorption edge. The minimum absorption coefficients measured varied somewhat with sample age and quality, but were typically in the range 1 cm{sup {minus}1} to 10 cm{sup {minus}1}. In the region below 1 eV, overtones of C-H stretching modes were observed, indicating that further improvements in transparency in this spectral region might be achieved via deuteration of fluorination.

  14. Regression of polyvinylchloride polymer pneumoconiosis

    OpenAIRE

    White, N W; Ehrlich, R. I.

    1997-01-01

    A 35 year old man heavily exposed to polyvinylchloride (PVC) polymer dust developed dyspnoea and a mild restrictive lung disorder consistent with PVC pneumoconiosis. Clinical and radiological abnormalities cleared on removal from exposure, suggesting that in its early stages PVC pneumoconiosis is reversible. 






  15. Radial distribution function in polymers

    Science.gov (United States)

    Przygocki, Wladyslaw

    1997-02-01

    Radial distribution function is a very useful tool for determination of the polymer structure. The connection between the scattered X-ray intensity and radial distribution function is presented. Some examples of RDF for polyethylene and for poly(ethylene terephtalate).

  16. Molecularly imprinted polymers for mycotoxins

    Science.gov (United States)

    Molecularly imprinted polymers (MIPs) are a class of synthetic receptors capable of selective recognition of analytes. Recent developments in imprinting technology have made it possible to apply this technology in a range of applications, including mycotoxin detection. Structure-activity relations...

  17. Polymer systems testing: Final report

    International Nuclear Information System (INIS)

    Los Alamos National Laboratory (LANL) is in the process of decontaminating lead shielding material. The procedure involves abrasive surface etching of the shielding to remove the outer layer of lead that contains the majority of the radioactive contaminants. This procedure generates a small volume of mixed waste in the form of a wet residue containing lead, abrasive grit (Al2O3), uranium and water. IC Technologies, Inc. (ICT) has developed several processes for the treatment of mixed wastes involving stabilizing/encapsulating the waste in a polymer monolith. The objective of the test program was to verify the applicability of ICT's technology to this specific waste stream and provide LANL baseline data on the performance of polymer encapsulation techniques. Polymer microencapsulation of lead shielding/blasting grit (surrogate) mixed waste was evaluated. Two polymers, melamine formaldehyde and polyester xylene, were used to examine the effect of waste loading on Toxicity Characteristic Leaching Procedure (TCLP) extract Pb concentration. Six levels of waste loading were evaluated by eleven tests. Significant reduction in Pb solubility during TCLP was achieved. Additional optimization to the single-stage microencapsulation technique utilized will be necessary to mitigate the toxic (RCRA) characteristic of the waste

  18. Agricultural Polymers as Corrosion Inhibitors

    Science.gov (United States)

    Agricultural polymers were composed of extra-cellular polysaccharides secreted by Leuconostoc mesenteroides have been shown to inhibit corrosion on corrosion-sensitive metals. The substantially pure exopolysaccharide has a general structure consisting of alpha(1-6)-linked D-glucose backbone and appr...

  19. Vapour pressure osmometry determination of water activity of binary and ternary aqueous (polymer + polymer) solutions

    International Nuclear Information System (INIS)

    Highlights: • VPO determination of water activity for binary and ternary aqueous polymer solutions. • Vapour pressure of binary and ternary aqueous polymer solutions were determined. • Water activities were correlated using the segment-based NRTL and Wilson models. • Molar Gibbs free energy changes due to mixing were determined. - Abstract: Precise water activity measurements at T = 308.15 K were carried out on several binary (water + polymer) and ternary {water + polymer (1) + polymer (2)} systems using the vapour pressure osmometry (VPO) technique. Polymers were polyethylene glycol 400 (PEG400), polyethylene glycol 6000 (PEG6000), polypropylene glycol 400 (PPG400), polyvinylpyrrolidone (PVP) and dextran (DEX). The water activity results obtained were used to calculate the vapour pressure of solutions as a function of concentration and the segment-based local composition models, NRTL and Wilson, were used to correlate the experimental water activity values. It was found that, for the polymer concentration range studied here, the values of the water activity obtained for the binary (water + polymer) solutions decrease in the order DEX > PVP > PEG6000 > PPG400 > PEG400. Furthermore, water activities of solutions of each polymer in the aqueous solutions of (5, 10, 15 and 20)% (w/w) other polymers investigated were also measured at T = 308.15 K. The ability of polymer (1) in decreasing the water activity of binary {water + polymer (2)} solutions was discussed on the basis of the (polymer + water) and {polymer (1) + polymer (2)} interactions

  20. Nanotribology of charged polymer brushes

    Science.gov (United States)

    Klein, Jacob

    Polymers at surfaces, whose modern understanding may be traced back to early work by Sam Edwards1, have become a paradigm for modification of surface properties, both as steric stabilizers and as remarkable boundary lubricants2. Charged polymer brushes are of particular interest, with both technological implications and especially biological relevance where most macromolecules are charged. In the context of biolubrication, relevant in areas from dry eye syndrome to osteoarthritis, charged polymer surface phases and their complexes with other macromolecules may play a central role. The hydration lubrication paradigm, where tenaciously-held yet fluid hydration shells surrounding ions or zwitterions serve as highly-efficient friction-reducing elements, has been invoked to understand the excellent lubrication provided both by ionized3 and by zwitterionic4 brushes. In this talk we describe recent advances in our understanding of the nanotribology of such charged brush systems. We consider interactions between charged end-grafted polymers, and how one may disentangle the steric from the electrostatic surface forces5. We examine the limits of lubrication by ionized brushes, both synthetic and of biological origins, and how highly-hydrated zwitterionic chains may provide extremely effective boundary lubrication6. Finally we describe how the lubrication of articular cartilage in the major joints, a tribosystem presenting some of the greatest challenges and opportunities, may be understood in terms of a supramolecular synergy between charged surface-attached polymers and zwitterionic groups7. Work supported by European Research Council (HydrationLube), Israel Science Foundation (ISF), Petroleum Research Fund of the American Chemical Society, ISF-NSF China Joint Program.

  1. System Applies Polymer Powder To Filament Tow

    Science.gov (United States)

    Baucom, Robert M.; Snoha, John J.; Marchello, Joseph M.

    1993-01-01

    Polymer powder applied uniformly and in continuous manner. Powder-coating system applies dry polymer powder to continuous fiber tow. Unique filament-spreading technique, combined with precise control of tension on fibers in system, ensures uniform application of polymer powder to web of spread filaments. Fiber tows impregnated with dry polymer powders ("towpregs") produced for preform-weaving and composite-material-molding applications. System and process valuable to prepreg industry, for production of flexible filament-windable tows and high-temperature polymer prepregs.

  2. Electrochemical Study of Conductive Gel Polymer

    Institute of Scientific and Technical Information of China (English)

    Zhaohui Li; Jing Jiang; Gangtie Lei

    2005-01-01

    @@ 1Introduction Conventional ion-conducting polymer consists of electrolyte salt and polymer matrix, so-called salt-inpolymer. It possesses lower conductivity because the migration of ions depends on the motion of polymer segmental. To increase the ionic conductivity, a kind of gel polymer film (GPF) was prepared by in situ polymerization of methyl methacrylate (MMA) monomer in room-temperature ionic liquid(RTIL), 1-butyl-3-methylimidazolium hexafluorophosphate (BMIPF6). Due to immeasurably low vapor pressure, high ionic conductivity, and greater thermal and electrochemical stability, BMIPF6 is suitable electrolyte salts for ion-conducting polymer.

  3. PolyGraph: a Polymer Visualization system

    Science.gov (United States)

    Cutkosky, Ashok; Tarazi, Najeeb; Lieberman Aiden, Erez

    2012-02-01

    Rapid advances in computational hardware and parallelization have made complex simulations of large polymers increasingly ubiquitous. However, visualizing such simulations remains a challenge. Here we present PolyGraph, a Blender-powered visualization system for complex polymer simulations. As a specific example, we study molecular dynamics simulations of condensing polymers. We illustrate our initial simulation results, suggesting that formation of local beads is an initial step in the condensation process. (This finding is consistent with earlier conjectures about polymer condensation.) PolyGraph makes it possible to create precise and visually appealing clips of polymer simulations. *contributed equally

  4. Synthesis of cyanopyridine based conjugated polymer

    Directory of Open Access Journals (Sweden)

    B. Hemavathi

    2016-06-01

    Full Text Available This data file contains the detailed synthetic procedure for the synthesis of two new cyanopyridine based conjugated polymer P1 and P2 along with the synthesis of its monomers. The synthesised polymers can be used for electroluminescence and photovoltaic (PV application. The physical data of the polymers are provided in this data file along with the morphological data of the polymer thin films. The data provided here are in association with the research article entitled ‘Cyanopyridine based conjugated polymer-synthesis and characterisation’ (Hemavathi et al., 2015 [3].

  5. Recent developments in intelligent biomedical polymers

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Intelligent polymers or stimuli-responsive polymers may exhibit distinct transitions in physical-chemical properties, including conformation, polarity, phase structure and chemical composition in response to changes in environmental stimuli. Due to their unique ’intelligent’ characteristics, stimuli-sensitive polymers have found a wide variety of applications in biomedical and nanotechnological fields. This review focuses on the recent developments in biomedical application of intelligent polymer systems, such as intelligent hydrogel systems, intelligent drug delivery systems and intelligent molecular recognition systems. Also, the possible future directions for the application of these intelligent polymer systems in the biomedical field are presented.

  6. Method of forming a foamed thermoplastic polymer

    Science.gov (United States)

    Duchane, D.V.; Cash, D.L.

    1984-11-21

    A solid thermoplastic polymer is immersed in an immersant solution comprising a compatible carrier solvent and an infusant solution containing an incompatible liquid blowing agent for a time sufficient for the immersant solution to infuse into the polymer. The carrier solvent is then selectively extracted, preferably by a solvent exchange process in which the immersant solution is gradually diluted with and replaced by the infusant solution, so as to selectively leave behind the infustant solution permanently entrapped in the polymer. The polymer is then heated to volatilize the blowing agent and expand the polymer into a foamed state.

  7. Recent developments in intelligent biomedical polymers

    Institute of Scientific and Technical Information of China (English)

    XIAO ChunSheng; TIAN HuaYu; ZHUANG XiuLi; CHEN XueSi; JING XiaBin

    2009-01-01

    Intelligent polymers or stimuli-responsive polymers may exhibit distinct transitions in physical-chemical properties, including conformation, polarity, phase structure and chemical composition in response to changes in environmental stimuli. Due to their unique 'intelligent' characteristics, stimuli-sensitive polymers have found a wide variety of applications in biomedical and nanotechnological fields. This review focuses on the recent developments in biomedical application of intelligent polymer systems, such as intelligent hydrogel systems, intelligent drug delivery systems and intelligent molecular recognition systems. Also, the possible future directions for the application of these intelligent polymer systems in the biomedical field are presented.

  8. Triazatruxene-containing hyperbranched polymers:Microwave-assisted synthesis and optoelectronic properties

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Hyperbranched polymer structures represent a class of high-functionality building blocks with excellent three-dimensional topology for the construction of highly substituted conjugated polymers.In this contribution,an efficient microwave synthesis protocol toward the synthesis of conjugated hyperbranched polymers is presented.A novel series of soluble hyperbranched polyfluorenes (PTF1-PTF3) incorporating triazatruxene moiety as the branch units with various branching degrees have thus been successfully constructed with good yields and high molecular weight via a facile "A2+B2+C3" approach.The structures of the hyperbranched polymers were confirmed by NMR and GPC.Their thermal,optical,and electrochemical properties of the hyperbranched polymers were also investigated.The results showed that introduction of triazatruxene units into the hyperbranched structure endowed the polymer with good thermal stability and highly amorphous properties.Photophysical investigation of PTFx revealed strong blue emission in both solution and solid states.Hyperbranched polymers with higher degree of branching and proper content of linear fluorene units exhibited better photophysical properties in terms of narrow emission spectra and relatively high quantum efficiency as well as improved thermal spectral stability.The triazatruxene branching unit also played a role in raising the HOMO energy levels relative to those of polyfluorenes that would help to improve the charge injection and transport properties.The incorporation of triazatruxene unit into hyperbranched polymers has thus explored an effective avenue for constructing optoelectronic polymers with improved functional characteristics.

  9. Radiation damage of polymers in ultrasonic fields

    International Nuclear Information System (INIS)

    Radiation damage has always been a topic of great interest in various fields of sciences. In this work, an attempt is made to probe into the effect of subthreshold ultrasonic waves on the radiation damage created by irradiation of deuterons in polymer samples wherein the polymer samples act as model systems. Two equal volumes of radiation damage were produced in a single polymer sample wherein a standing wave of ultrasound was introduced into one. Three polymers namely, Polycarbonate, Polymethylmethacrylate and Polyvinyl chloride were used in this work. Four independent techniques were used to analyze the irradiated samples and visualize the radiation damage. Interferometric measurements give a measure of the refractive index modulation in the irradiated sample. Polymers, being transparent, do not absorb in the visible region of the electromagnetic spectrum. UV-Vis absorption spectroscopy shows absorption peaks in the visible region in irradiated polymer samples. Ion irradiation causes coloration of polymers. The light microscope is used to measure the absorption of white light by the irradiated polymers. Positron annihilation spectroscopy is used to obtain a measure of the open volume created by irradiation in polymers. A comparison between the irradiated region and the region exposed to ultrasonic waves simultaneously with irradiation in a polymer sample shows the polymer specific influence of the ultrasonic standing wave. (orig.)

  10. Radiation damage of polymers in ultrasonic fields

    Energy Technology Data Exchange (ETDEWEB)

    Anbalagan, Poornnima

    2008-07-01

    Radiation damage has always been a topic of great interest in various fields of sciences. In this work, an attempt is made to probe into the effect of subthreshold ultrasonic waves on the radiation damage created by irradiation of deuterons in polymer samples wherein the polymer samples act as model systems. Two equal volumes of radiation damage were produced in a single polymer sample wherein a standing wave of ultrasound was introduced into one. Three polymers namely, Polycarbonate, Polymethylmethacrylate and Polyvinyl chloride were used in this work. Four independent techniques were used to analyze the irradiated samples and visualize the radiation damage. Interferometric measurements give a measure of the refractive index modulation in the irradiated sample. Polymers, being transparent, do not absorb in the visible region of the electromagnetic spectrum. UV-Vis absorption spectroscopy shows absorption peaks in the visible region in irradiated polymer samples. Ion irradiation causes coloration of polymers. The light microscope is used to measure the absorption of white light by the irradiated polymers. Positron annihilation spectroscopy is used to obtain a measure of the open volume created by irradiation in polymers. A comparison between the irradiated region and the region exposed to ultrasonic waves simultaneously with irradiation in a polymer sample shows the polymer specific influence of the ultrasonic standing wave. (orig.)

  11. A Platform for Functional Conductive Polymers

    DEFF Research Database (Denmark)

    Daugaard, Anders Egede; Hoffmann, Christian; Lind, Johan Ulrik;

    Conductive polymers have been studied extensively during recent years. In order to broaden the application field of conductive polymers different methods have been tested and recently an azide functional poly(3,4-ethylenedioxythiophene) (PEDOT-N3) was developed(1, 2). The azide functional...... conductive polymer can be postpolymerization functionalized to introduce a large number of functionalities through click chemistry(3). Through selection of reaction conditions it is possible control the depth of the reaction into the polymer film to the upper surface or the entire film(4). Thus a conductive...... polymer can be prepared with a subsurface layer of highly conductive polymer where only the upper surface has been grafted with functional groups to ensure selectivity of the surface layer for e.g. interaction with specific biospecies. The conductive polymer can be patterned using selective etching, which...

  12. Active Polymers Confer Fast Reorganization Kinetics

    CERN Document Server

    Swanson, Douglas

    2011-01-01

    Many cytoskeletal biopolymers are "active," consuming energy in large quantities. In this Letter, we identify a fundamental difference between active polymers and passive, equilibrium polymers: for equal mean lengths, active polymers can reorganize faster than equilibrium polymers. We show that equilibrium polymers are intrinsically limited to linear scaling between mean lifetime and mean length, MFPT ~ , by analogy to 1-d Potts models. By contrast, we present a simple active-polymer model that improves upon this scaling, such that MFPT ~ ^{1/2}. Since to be biologically useful, structural biopolymers must typically be many monomers long, yet respond dynamically to the needs of the cell, the difference in reorganization kinetics may help to justify active polymers' greater energy cost. PACS numbers: 87.10.Ed, 87.16.ad, 87.16.Ln

  13. Ending Aging in Super Glassy Polymer Membranes

    Energy Technology Data Exchange (ETDEWEB)

    Lau, CH; Nguyen, PT; Hill, MR; Thornton, AW; Konstas, K; Doherty, CM; Mulder, RJ; Bourgeois, L; Liu, ACY; Sprouster, DJ; Sullivan, JP; Bastow, TJ; Hill, AJ; Gin, DL; Noble, RD

    2014-04-16

    Aging in super glassy polymers such as poly(trimethylsilylpropyne) (PTMSP), poly(4-methyl-2-pentyne) (PMP), and polymers with intrinsic microporosity (PIM-1) reduces gas permeabilities and limits their application as gas-separation membranes. While super glassy polymers are initially very porous, and ultra-permeable, they quickly pack into a denser phase becoming less porous and permeable. This age-old problem has been solved by adding an ultraporous additive that maintains the low density, porous, initial stage of super glassy polymers through absorbing a portion of the polymer chains within its pores thereby holding the chains in their open position. This result is the first time that aging in super glassy polymers is inhibited whilst maintaining enhanced CO2 permeability for one year and improving CO2/N-2 selectivity. This approach could allow super glassy polymers to be revisited for commercial application in gas separations.

  14. Polymer dynamics in nanoconfinement: Interfaces and interphases

    Directory of Open Access Journals (Sweden)

    Krutyeva Margarita

    2015-01-01

    Full Text Available The dynamics of polymers in nanoconfinement was studied by using neutron spectroscopy. A number of pronounced effects on different time and length scales for the polymers confined in nanopores of anodic aluminium oxide were observed. Local segmental dynamics was found to be dependent on the type of the interaction between the solid pore wall and polymer: attractive interactions lead to the formation of a surface layer with the dynamics slowed down as compared to the dynamics of pure polymer; neutral/repulsive interaction do not change the local dynamics. Attractive interactions cause anchoring of polymer segments on the surface creating an interphase between the polymer in close vicinity to the solid surface and pure polymer. In addition, at strong confinement conditions the dilution of the entanglement network is observed.

  15. Biodegradable Polyphosphazene Based Peptide-Polymer Hybrids

    Directory of Open Access Journals (Sweden)

    Anne Linhardt

    2016-04-01

    Full Text Available A novel series of peptide based hybrid polymers designed to undergo enzymatic degradation is presented, via macrosubstitution of a polyphosphazene backbone with the tetrapeptide Gly-Phe-Leu-Gly. Further co-substitution of the hybrid polymers with hydrophilic polyalkylene oxide Jeffamine M-1000 leads to water soluble and biodegradable hybrid polymers. Detailed degradation studies, via 31P NMR spectroscopy, dynamic light scattering and field flow fractionation show the polymers degrade via a combination of enzymatic, as well as hydrolytic pathways. The peptide sequence was chosen due to its known property to undergo lysosomal degradation; hence, these degradable, water soluble polymers could be of significant interest for the use as polymer therapeutics. In this context, we investigated conjugation of the immune response modifier imiquimod to the polymers via the tetrapeptide and report the self-assembly behavior of the conjugate, as well as its enzymatically triggered drug release behavior.

  16. Coating of fertilizers by degradable polymers.

    Science.gov (United States)

    Devassine, M; Henry, F; Guerin, P; Briand, X

    2002-08-21

    The conventional agriculture leads to some important pollution of ground water (particularly, by nitrates). The solution is the coating of fertilizers by degradable polymers. In this work, we have studied the water vapour and liquid diffusion through polymer films detached from their support. Therefore, we may classify polymers as a function of their properties like water vapour and liquid barrier. We may choose the best polymer(s) for coating.coated fertilizers by chosen polymer(s) with mechanical techniques such as fluidised bed and pan coating. Moreover, the electron microscopy used to see the quality of the wall has showed the presence of pores due to the rapid evaporation of solvent. A drying in air current and an annealing could be done to avoid this problem.followed the ions release of fertilizers immersed in distilled water by conductimetry. The more interesting result was obtained with fertilizers coated by polylactic acid. In effect, the total release reached three weeks.

  17. Water equivalence of polymer gel dosimeters

    International Nuclear Information System (INIS)

    To evaluate the water equivalence and radiation transport properties of polymer gel dosimeters over the wide range of photon and electron energies 14 different types of polymer gels were considered. Their water equivalence was evaluated in terms of effective atomic number (Zeff), electron density (ρe), photon mass attenuation coefficient (μ/ρ), photon mass energy absorption coefficient (μen/ρ) and total stopping power (S/ρ)tot of electrons using the XCOM and the ESTAR database. The study showed that the effective atomic number of polymer gels were very close (en/ρ for all polymer gels were in close agreement (tot of electrons in polymer gel dosimeters were within 1% agreement with that of water. From the study we conclude that at lower energy (<80keV) the polymer gel dosimeters cannot be considered water equivalent and study has to be carried out before using the polymer gel for clinical application

  18. Polymer blend compositions and methods of preparation

    Energy Technology Data Exchange (ETDEWEB)

    Naskar, Amit K.

    2016-09-27

    A polymer blend material comprising: (i) a first polymer containing hydrogen bond donating groups having at least one hydrogen atom bound to a heteroatom selected from oxygen, nitrogen, and sulfur, or an anionic version of said first polymer wherein at least a portion of hydrogen atoms bound to a heteroatom is absent and replaced with at least one electron pair; (ii) a second polymer containing hydrogen bond accepting groups selected from nitrile, halogen, and ether functional groups; and (iii) at least one modifying agent selected from carbon particles, ether-containing polymers, and Lewis acid compounds; wherein, if said second polymer contains ether functional groups, then said at least one modifying agent is selected from carbon particles and Lewis acid compounds. Methods for producing the polymer blend, molded forms thereof, and articles thereof, are also described.

  19. Stable trifluorostyrene containing compounds grafted to base polymers, and their use as polymer electrolyte membranes

    Science.gov (United States)

    Yang, Zhen-Yu; Roelofs, Mark Gerrit

    2010-11-09

    A fluorinated ion exchange polymer prepared by grafting at least one grafting monomer on to at least one base polymer, wherein the grafting monomer comprises structure 1a or 1b: wherein Z comprises S, SO.sub.2, or POR wherein R comprises a linear or branched perfluoroalkyl group of 1 to 14 carbon atoms optionally containing oxygen or chlorine, an alkyl group of 1 to 8 carbon atoms, an aryl group of 6 to 12 carbon atoms or a substituted aryl group of 6 to 12 carbon atoms; RF comprises a linear or branched perfluoroalkene group of 1 to 20 carbon atoms, optionally containing oxygen or chlorine; Q is chosen from F, --OM, NH.sub.2, --N(M)SO.sub.2R.sup.2.sub.F, and C(M)(SO.sub.2R.sup.2.sub.F).sub.2, wherein M comprises H, an alkali cation, or ammonium; R.sup.2.sub.F groups comprises alkyl of 1 to 14 carbon atoms which may optionally include ether oxygens or aryl of 6 to 12 carbon atoms where the alkyl or aryl groups may be perfluorinated or partially fluorinated; and n is 1 or 2 for 1a, and n is 1, 2, or 3 for 1b. These ion exchange polymers are useful in preparing catalyst coated membranes and membrane electrode assemblies used in fuel cells.

  20. Multiscale modeling of polymer nanocomposites

    Science.gov (United States)

    Sheidaei, Azadeh

    In recent years, polymer nano-composites (PNCs) have increasingly gained more attention due to their improved mechanical, barrier, thermal, optical, electrical and biodegradable properties in comparison with the conventional micro-composites or pristine polymer. With a modest addition of nanoparticles (usually less than 5wt. %), PNCs offer a wide range of improvements in moduli, strength, heat resistance, biodegradability, as well as decrease in gas permeability and flammability. Although PNCs offer enormous opportunities to design novel material systems, development of an effective numerical modeling approach to predict their properties based on their complex multi-phase and multiscale structure is still at an early stage. Developing a computational framework to predict the mechanical properties of PNC is the focus of this dissertation. A computational framework has been developed to predict mechanical properties of polymer nano-composites. In chapter 1, a microstructure inspired material model has been developed based on statistical technique and this technique has been used to reconstruct the microstructure of Halloysite nanotube (HNT) polypropylene composite. This technique also has been used to reconstruct exfoliated Graphene nanoplatelet (xGnP) polymer composite. The model was able to successfully predict the material behavior obtained from experiment. Chapter 2 is the summary of the experimental work to support the numerical work. First, different processing techniques to make the polymer nanocomposites have been reviewed. Among them, melt extrusion followed by injection molding was used to manufacture high density polyethylene (HDPE)---xGnP nanocomposties. Scanning electron microscopy (SEM) also was performed to determine particle size and distribution and to examine fracture surfaces. Particle size was measured from these images and has been used for calculating the probability density function for GNPs in chapter 1. A series of nanoindentation tests have

  1. Polymer compositions, polymer films and methods and precursors for forming same

    Science.gov (United States)

    Klaehn, John R; Peterson, Eric S; Orme, Christopher J

    2013-09-24

    Stable, high performance polymer compositions including polybenzimidazole (PBI) and a melamine-formaldehyde polymer, such as methylated, poly(melamine-co-formaldehyde), for forming structures such as films, fibers and bulky structures. The polymer compositions may be formed by combining polybenzimidazole with the melamine-formaldehyde polymer to form a precursor. The polybenzimidazole may be reacted and/or intertwined with the melamine-formaldehyde polymer to form the polymer composition. For example, a stable, free-standing film having a thickness of, for example, between about 5 .mu.m and about 30 .mu.m may be formed from the polymer composition. Such films may be used as gas separation membranes and may be submerged into water for extended periods without crazing and cracking. The polymer composition may also be used as a coating on substrates, such as metal and ceramics, or may be used for spinning fibers. Precursors for forming such polymer compositions are also disclosed.

  2. Silica/Polymer and Silica/Polymer/Fiber Composite Aerogels

    Science.gov (United States)

    Ou, Danny; Stepanian, Christopher J.; Hu, Xiangjun

    2010-01-01

    Aerogels that consist, variously, of neat silica/polymer alloys and silica/polymer alloy matrices reinforced with fibers have been developed as materials for flexible thermal-insulation blankets. In comparison with prior aerogel blankets, these aerogel blankets are more durable and less dusty. These blankets are also better able to resist and recover from compression . an important advantage in that maintenance of thickness is essential to maintenance of high thermal-insulation performance. These blankets are especially suitable as core materials for vacuum- insulated panels and vacuum-insulated boxes of advanced, nearly seamless design. (Inasmuch as heat leakage at seams is much greater than heat leakage elsewhere through such structures, advanced designs for high insulation performance should provide for minimization of the sizes and numbers of seams.) A silica/polymer aerogel of the present type could be characterized, somewhat more precisely, as consisting of multiply bonded, linear polymer reinforcements within a silica aerogel matrix. Thus far, several different polymethacrylates (PMAs) have been incorporated into aerogel networks to increase resistance to crushing and to improve other mechanical properties while minimally affecting thermal conductivity and density. The polymethacrylate phases are strongly linked into the silica aerogel networks in these materials. Unlike in other organic/inorganic blended aerogels, the inorganic and organic phases are chemically bonded to each other, by both covalent and hydrogen bonds. In the process for making a silica/polymer alloy aerogel, the covalent bonds are introduced by prepolymerization of the methacrylate monomer with trimethoxysilylpropylmethacrylate, which serves as a phase cross-linker in that it contains both organic and inorganic monomer functional groups and hence acts as a connector between the organic and inorganic phases. Hydrogen bonds are formed between the silanol groups of the inorganic phase and the

  3. Colloidal QDs-polymer nanocomposites

    Science.gov (United States)

    Gordillo, H.; Suárez, I.; Rodríguez-Cantó, P.; Abargues, R.; García-Calzada, R.; Chyrvony, V.; Albert, S.; Martínez-Pastor, J.

    2012-04-01

    Nanometer-size colloidal semiconductor nanocrystals, or Quantum Dots (NQD), are very prospective active centers because their light emission is highly efficient and temperature-independent. Nanocomposites based on the incorporation of QDs inside a polymer matrix are very promising materials for application in future photonic devices because they combine the properties of QDs with the technological feasibility of polymers. In the present work some basic applications of these new materials have been studied. Firstly, the fabrication of planar and linear waveguides based on the incorporation of CdS, CdSe and CdTe in PMMA and SU-8 are demonstrated. As a result, photoluminescence (PL) of the QDs are coupled to a waveguide mode, being it able to obtain multicolor waveguiding. Secondly, nanocomposite films have been evaluated as photon energy down-shifting converters to improve the efficiency of solar cells.

  4. Internal dissipation of a polymer.

    Science.gov (United States)

    Deutsch, J M

    2010-06-01

    The dynamics of flexible polymer molecules are often assumed to be governed by hydrodynamics of the solvent. However there is considerable evidence that internal dissipation of a polymer contributes as well. Here we investigate the dynamics of a single chain in the absence of solvent to characterize the nature of this internal friction. We model the chains as freely hinged but with localized bond angles and threefold symmetric dihedral angles. We show that the damping is close but not identical to Kelvin damping, which depends on the first temporal and second spatial derivative of monomer position. With no internal potential between monomers, the magnitude of the damping is small for long wavelengths and weakly damped oscillatory time dependent behavior is seen for a large range of spatial modes. When the size of the internal potential is increased, such oscillations persist, but the damping becomes larger. However underdamped motion is present even with quite strong dihedral barriers for long enough wavelengths. PMID:20866433

  5. Biological activity of ionene polymers

    Science.gov (United States)

    Rembaum, A.

    1973-01-01

    Ionene polymers are polyammonium salts with positive nitrogens in the backbone, resulting from the polycondensation of diamines with dihalides or from the polycondensation of halo amines. The mechanism of formation of ionene polymers of different structures and their biological activity is reviewed. The antimicrobial and antifungal properties are compared with low molecular weight ammonium salts. Ionenes were found to combine with DNA by means of ionic bonds to yield similar complexes to those obtained with polyamines (spermine and spermidine). They also combine with nerve cell receptors and exercise a more powerful and longer duration ganglionic blocking action than their monomeric analogs. The antiheparin activity of ionenes and the thromboresistance of elastomeric ionene heparin coatings is described. The enhanced biological activity of ionenes as compared with low molecular weight compounds is attributed to a cooperative effect of a large number of positive charges on the polymeric chains.

  6. Polymer-clay Nano Composites

    Directory of Open Access Journals (Sweden)

    R. S. Chauhan

    2006-10-01

    Full Text Available Nano has now become a theme in almost all the established discipline. The confluence ofinnovative methodologies, sophisticated characterisation techniques, and potential technologicalutility has resulted in intense research activity in the field of polymer nano composites. Polymercomposites made out of nano materials display unique properties in terms of improved tensilestrength, flexibility, and flexural endurance. The paper discusses the development of polymerclaynano composites, both from the conceptual point of view as well as practical methods forthe synthesis of nano composites. These are monomer intercalation, monomer modification,common solvent, and melt-intercalation methods. Various models have been discussed thatdescribe improvements in mechanical and barriers properties due to the incorporation of nanomaterials. Ongoing R&D work in the two DRDO laboratories on the development of nanocomposites has been briefly mentioned. The emerging use of polymer-nano composites has alsobeen described.

  7. Polymer-Layer Silicate Nanocomposites

    DEFF Research Database (Denmark)

    Potarniche, Catalina-Gabriela

    with a spectacular improvement up to 300 % in impact strength were obtained. In the second part of this study, layered silicate bio-nanomaterials were obtained starting from natural compounds and taking into consideration their biocompatibility properties. These new materials may be used for drug delivery systems......Nowadays, some of the material challenges arise from a performance point of view as well as from recycling and biodegradability. Concerning these aspects, the development of polymer layered silicate nanocomposites can provide possible solutions. This study investigates how to obtain polymer layered...... toughness-stiffness requirements. The new compatibilizer system used to obtain nanocomposites, presented an improvement of 8-20 % in tensile strength, 15-34 % in Young’s modulus, 23-34 % in fatigue tests and 20-58% in degree of crystalline phase. By introducing a rubbery phase as modifier, nanocomposites...

  8. Design of electrically conducting polymer hybrid composites based on polyvinyl chloride and polyethylene

    OpenAIRE

    Kuryptya, Yaroslav; Sova, Nadiya; Savchenko, Bohdan; Slieptsov, Aleksander; Plavan, Viktoriia

    2016-01-01

    Interest to electrically conducting polymer composite materials in recent times has grown considerably, which is associated with the design of new branches of science and technology. The existing analogues are different in the complexity of production and high cost. One of the ways of solving the problem may be designing polymer composite materials with a combined filler. The research was carried out on creating electrically conducting hybrid polymer composites, based on emulsion polyvinyl ch...

  9. Inclusion and functionalization of polymers with cyclodextrins: current applications and future prospects.

    Science.gov (United States)

    Folch-Cano, Christian; Yazdani-Pedram, Mehrdad; Olea-Azar, Claudio

    2014-01-01

    The numerous hydroxyl groups available in cyclodextrins are active sites that can form different types of linkages. They can be crosslinked with one another, or they can be derivatized to produce monomers that can form linear or branched networks. Moreover, they can form inclusion complexes with polymers and different substrates, modifying their physicochemical properties. This review shows the different applications using polymers with cyclodextrins, either by forming inclusion complexes, ternary complexes, networks, or molecularly imprinted polymers (MIPs). On one hand, the use of cyclodextrins enhances the properties of each polymer, and on the other the use of polymers decreases the amount of cyclodextrins required in different formulations. Both cyclodextrins and polymers contribute synergistically in several applications such as pharmacological, nutritional, environmental, and other industrial fields. The use of polymers based on cyclodextrins is a low cost easy to use potential tool with great future prospects.

  10. Inclusion and Functionalization of Polymers with Cyclodextrins: Current Applications and Future Prospects

    Directory of Open Access Journals (Sweden)

    Christian Folch-Cano

    2014-09-01

    Full Text Available The numerous hydroxyl groups available in cyclodextrins are active sites that can form different types of linkages. They can be crosslinked with one another, or they can be derivatized to produce monomers that can form linear or branched networks. Moreover, they can form inclusion complexes with polymers and different substrates, modifying their physicochemical properties. This review shows the different applications using polymers with cyclodextrins, either by forming inclusion complexes, ternary complexes, networks, or molecularly imprinted polymers (MIPs. On one hand, the use of cyclodextrins enhances the properties of each polymer, and on the other the use of polymers decreases the amount of cyclodextrins required in different formulations. Both cyclodextrins and polymers contribute synergistically in several applications such as pharmacological, nutritional, environmental, and other industrial fields. The use of polymers based on cyclodextrins is a low cost easy to use potential tool with great future prospects.

  11. Synthesis and characterizations of novel polymer electrolytes

    Science.gov (United States)

    Chanthad, Chalathorn

    end-blocks is described for the first time. The synthetic strategy involves the preparation of the telechelic fluoropolymers using a functional benzoyl peroxide initiator as the macro-chain transfer agent for subsequent RAFT polymerization of the imidazolium methacrylate monomer. As revealed in DSC, SAXS and dielectric relaxation spectroscopy (DRS) measurements, there was no microphase separation in the triblock copolymers, likely due to solubility of ionic liquid moieties in the fluoropolymer matrix. The anionic counterion has direct impact on the thermal properties, ionic conductivity and segmental dynamics of the polymers. The temperature dependence of the ionic conductivity is well described by the Vogel-Tamman-Fulcher model, suggesting that ion motion is closely coupled to segmental motion. In Chapter 4 and 5, new solid electrolytes for lithium cations have been synthesized by catalyzed hydrosilylation reaction involving hydrogen atoms of polysiloxane and polyhedral oligomeric silsesquioxane (POSS) and double bonds of vinyl tris17-bromo-3,6,9,12,15- pentaoxaheptadecan-1-ol silane. The obtained structures are based on branched or dendritic with ionic liquid-ethylene oxide oligomer. High room temperature ionic conductivities have been obtained in the range of 10-4-10-5 can be regarded as solid electrolytes. This is attributed to the high concentration of ions from ionic liquid moieties in the tripodand molecule, high segmental mobility, and high ion dissociation from ethylene oxide spacers. The influence of anion structures and lithium salts and concentration has been investigated.

  12. Hydrogen Bonds in Polymer Folding

    OpenAIRE

    Borg, J; Jensen, M. H.; K. Sneppen; Tiana, G.

    2000-01-01

    The thermodynamics of a homopolymeric chain with both Van der Waals and highly-directional hydrogen bond interaction is studied. The effect of hydrogen bonds is to reduce dramatically the entropy of low-lying states and to give raise to long-range order and to conformations displaying secondary structures. For compact polymers a transition is found between helix-rich states and low-entropy sheet-dominated states. The consequences of this transition for protein folding and, in particular, for ...

  13. Topical Review: Polymer gel dosimetry

    OpenAIRE

    Baldock, C; De Deene, Y; Doran, S.; Ibbott, G; Jirasek, A.; Lepage, M.; McAuley, K B; Oldham, M; Schreiner, L J

    2010-01-01

    Polymer gel dosimeters are fabricated from radiation sensitive chemicals which, upon irradiation, polymerize as a function of the absorbed radiation dose. These gel dosimeters, with the capacity to uniquely record the radiation dose distribution in three-dimensions (3D), have specific advantages when compared to one-dimensional dosimeters, such as ion chambers, and two-dimensional dosimeters, such as film. These advantages are particularly significant in dosimetry situations where steep dose ...

  14. Diamond turning of thermoplastic polymers

    Energy Technology Data Exchange (ETDEWEB)

    Smith, E.; Scattergood, R.O.

    1988-12-01

    Single point diamond turning studies were made using a series of thermoplastic polymers with different glass transition temperatures. Variations in surface morphology and surface roughness were observed as a function of cutting speed. Lower glass transition temperatures facilitate smoother surface cuts and better surface finish. This can be attributed to the frictional heating that occurs during machining. Because of the very low glass transition temperatures in polymeric compared to inorganic glasses, the precision machining response can be very speed sensitive.

  15. Methods of polymer binder examination

    OpenAIRE

    M. Holtzer; B. Grabowska; Bobrowski, A.

    2010-01-01

    This article presents selected methods of examining polymer binders (in particular current or promising ones), including spectroscopy, microscopy, nanometry, chromatography and thermal analysis. The table (containing 23 literature references) collates and generally characterises over 20 analytical methods from the above groups. In addition, information is presented on research conducted by the Environmental Protection Lab of the Chair of Casting Process Engineering, Faculty of Foundry Enginee...

  16. Polymer biocomposites with renewable sources

    OpenAIRE

    S. Kuciel; P. Kuźniar; A. Liber-Kneć

    2010-01-01

    Nowadays production of natural biodegradable polymer composites is an important research topic on the stage of renewable sourcesimplementation instead of petrochemical sources. In this work, possibilities of processing biocomposites on the base on different types of biopolymers – polylactide (PLA), thermoplastic starch (TPS), polyhydroxybutyrate (PHB), cellulose acetate (CA) - filled with natural fibers such as wood, kenaf, horse hair and nettle are presented. Large variety of natural fibers ...

  17. Endotoxin hitchhiking on polymer nanoparticles

    Science.gov (United States)

    Donnell, Mason L.; Lyon, Andrew J.; Mormile, Melanie R.; Barua, Sutapa

    2016-07-01

    The control of microbial infections is critical for the preparation of biological media including water to prevent lethal septic shock. Sepsis is one of the leading causes of death in the United States. More than half a million patients suffer from sepsis every year. Both gram-positive and gram-negative bacteria are responsible for septic infection by the most common organisms i.e., Escherichia coli and Pseuodomonas aeruginosa. The bacterial cell membrane releases negatively charged endotoxins upon death and enzymatic destruction, which stimulate antigenic response in humans to gram-negative infections. Several methods including distillation, ethylene oxide treatment, filtration and irradiation have been employed to remove endotoxins from contaminated samples, however, the reduction efficiency remains low, and presents a challenge. Polymer nanoparticles can be used to overcome the current inability to effectively sequester endotoxins from water. This process is termed endotoxin hitchhiking. The binding of endotoxin on polymer nanoparticles via electrostatic and hydrophobic interactions offers efficient removal from water. However, the effect of polymer nanoparticles and its surface areas has not been investigated for removal of endotoxins. Poly(ε-caprolactone) (PCL) polymer was tested for its ability to effectively bind and remove endotoxins from water. By employing a simple one-step phase separation technique, we were able to synthesize PCL nanoparticles of 398.3 ± 95.13 nm size and a polydispersity index of 0.2. PCL nanoparticles showed ∼78.8% endotoxin removal efficiency, the equivalent of 3.9 × 105 endotoxin units (EU) per ml. This is 8.34-fold more effective than that reported for commercially available membranes. Transmission electron microscopic images confirmed binding of multiple endotoxins to the nanoparticle surface. The concept of using nanoparticles may be applicable not only to eliminate gram-negative bacteria, but also for any gram

  18. Supramolecular Polymers in DNA Nanotechnology

    OpenAIRE

    Vyborna, Yuliia; Vybornyi, Mykhailo; Häner, Robert

    2016-01-01

    Creation of biocompatible functional materials is an important task in supramolecular chemistry. In this contribution, we report on noncovalent synthesis of DNA-grafted supramolecular polymers (SPs). DNA-grafted SPs enable programmed arrangement of oligonucleotides in a regular, tightly packed one-dimensional array. Further interactions of DNA-grafted SPs with complementary DNA strands leads to the formation of networks through highly cooperative G-C blunt-end stacking interactions. The struc...

  19. Wetting of polymer covered surfaces

    OpenAIRE

    Halperin, A.; De Gennes, P.G.

    1986-01-01

    We consider solid surfaces, partly covered with flexible, neutral, linear polymers (by adsorption or by grafting), wetted by a liquid which is a good solvent of the poymer. We give formulae for the spreading coefficient S as a function of chain length, solvent quality and adsorption strength. We also discuss the wetting films obtained in spreading a droplet of (non volatile) solvent : the equilibrium thickness e of the film is a compromise between S (favouring thin films) and the coil entropi...

  20. Foaming behaviour of polymer-surfactant solutions

    International Nuclear Information System (INIS)

    We study the effect of a non-ionic amphiphilic polymer (PEG-100 stearate also called Myrj 59) on the foaming behaviour of aqueous solutions of an anionic surfactant (sodium dodecyl sulfate or SDS). The SDS concentration was kept fixed while the Myrj 59 concentration was varied. Measurements of foamability, surface tension and electrical conductivity were carried out. The results show two opposite effects depending on the polymer concentration: foamability is higher when the Myrj 59 concentration is low; however, it decreases considerably when the polymer concentration is increased. This behaviour is due to the polymer adsorption at the air/liquid interface at lower polymer concentrations, and to the formation of a polymer-surfactant complex in the bulk at higher concentrations. The results are confirmed by surface tension and electrical conductivity measurements, which are interpreted in terms of the microstructure of the polymer-surfactant solutions. The observed behaviour is due to the amphiphilic nature of the studied polymer. The increased hydrophobicity of Myrj 59, compared to that of water-soluble polymers like PEG or PEO, increases its 'reactivity' towards SDS, i.e. the strength of its interaction with this anionic surfactant. Our results show that hydrophobically modified polymers have potential applications as additives in order to control the foaming properties of surfactant solutions

  1. Mechanical properties of hybrid polymer nanotube systems

    Science.gov (United States)

    Coleman, Jonathan N.; Cadek, Martin; Dalton, Alan B.; Munoz, Edgar; Razal, Joselito; Baughman, Ray H.; Blau, Werner J.

    2003-04-01

    In this work, mechanical properties of hybrid materials fabricated from nanotubes and commercially available polymers were investigated. It was found that, by adding various concentrations of arc discharge multiwall nanotubes, both Young"s modulus and hardness increased by factors of 1.8 and 1.6 at 1wt% in PVA and 2.8 and 2.0 at 8wt% in PVK, in reasonable agreement with the Halpin-Tsai theory. Furthermore, the presence of the nanotubes was found to nucleate crystallization of the PVA. This crystal growth is thought to enhance matrix-nanotube stress transfer. In addition, microscopy studies suggest extremely strong interfacial bonding in the PVA-based composite. This is manifested by the fracture of the polymer rather that the polymer-nanotube interface. The dependence of the polymer nanotube interfacial interaction on host polymer was studied by intercalating various polymers (PVA, PVP and PS) into single wall nanotube buckypaper. Even for short soak times, significant polymer intercalation into existing free volume was observed. Depending on the polymer and the level of intercalation tensile tests on intercalated sheets showed that the Young"s modulus, strength and toughness increased by factors of 3, 9 and 28, respectively. This indicates that the intercalated polymer enhances load transmission between nanotubes due the significant stress transfer. The level of stress transfer was observed to scale with polymer hydrophobicity as expected.

  2. Antimicrobial Polymers with Metal Nanoparticles

    Directory of Open Access Journals (Sweden)

    Humberto Palza

    2015-01-01

    Full Text Available Metals, such as copper and silver, can be extremely toxic to bacteria at exceptionally low concentrations. Because of this biocidal activity, metals have been widely used as antimicrobial agents in a multitude of applications related with agriculture, healthcare, and the industry in general. Unlike other antimicrobial agents, metals are stable under conditions currently found in the industry allowing their use as additives. Today these metal based additives are found as: particles, ions absorbed/exchanged in different carriers, salts, hybrid structures, etc. One recent route to further extend the antimicrobial applications of these metals is by their incorporation as nanoparticles into polymer matrices. These polymer/metal nanocomposites can be prepared by several routes such as in situ synthesis of the nanoparticle within a hydrogel or direct addition of the metal nanofiller into a thermoplastic matrix. The objective of the present review is to show examples of polymer/metal composites designed to have antimicrobial activities, with a special focus on copper and silver metal nanoparticles and their mechanisms.

  3. Supramolecular nesting of cyclic polymers

    Science.gov (United States)

    Kondratuk, Dmitry V.; Perdigão, Luís M. A.; Esmail, Ayad M. S.; O'Shea, James N.; Beton, Peter H.; Anderson, Harry L.

    2015-04-01

    Advances in template-directed synthesis make it possible to create artificial molecules with protein-like dimensions, directly from simple components. These synthetic macromolecules have a proclivity for self-organization that is reminiscent of biopolymers. Here, we report the synthesis of monodisperse cyclic porphyrin polymers, with diameters of up to 21 nm (750 C-C bonds). The ratio of the intrinsic viscosities for cyclic and linear topologies is 0.72, indicating that these polymers behave as almost ideal flexible chains in solution. When deposited on gold surfaces, the cyclic polymers display a new mode of two-dimensional supramolecular organization, combining encapsulation and nesting; one nanoring adopts a near-circular conformation, thus allowing a second nanoring to be captured within its perimeter, in a tightly folded conformation. Scanning tunnelling microscopy reveals that nesting occurs in combination with stacking when nanorings are deposited under vacuum, whereas when they are deposited directly from solution under ambient conditions there is stacking or nesting, but not a combination of both.

  4. Spontaneous Vesicles Modulated by Polymers

    Directory of Open Access Journals (Sweden)

    Francisco Ortega

    2011-08-01

    Full Text Available Vesicles are widely used in technological applications including cosmetic products, in microencapsulation for drug delivery, as anticancer agents and in the technology of adhesives, paints and inks. The vesicle size and the surface charge are very important properties from a technological point of view. Thus, the challenge in formulation is to find inexpensive stable vesicles with well-defined sizes and to modulate the surface charge of these aggregates. In this work we analyze the effect of different polymers on the structural properties of vesicles of the biodegradable surfactant sodium bis(2-ethyl-hexyl sulfosuccinate, Aerosol OT. Using fluorescence, conductivity, electrophoretic mobility and dynamic light scattering measurements we study the effect of the polymer nature, molecular weight and polymer concentration on the stability and the vesicle size properties. Results demonstrate that it is possible to modulate both the size and the electric surface charge of spontaneous vesicles of Aerosol OT by the addition of very small percentages of poly(allylamine and poly(maleic anhydride-alt-1-octadecen.

  5. Turbulence of Dilute Polymer Solution

    CERN Document Server

    Xi, Heng-Dong; Xu, Haitao

    2013-01-01

    In fully developed three dimensional fluid turbulence the fluctuating energy is supplied at large scales, cascades through intermediate scales, and dissipates at small scales. It is the hallmark of turbulence that for intermediate scales, in the so called inertial range, the average energy flux is constant and independent of viscosity [1-3]. One very important question is how this range is altered, when an additional agent that can also transport energy is added to the fluid. Long-chain polymers dissolved at very small concentrations in the fluid are such an agent [4,5]. Based on prior work by de Gennes and Tabor [6,7] we introduce a theory that balances the energy flux through the turbulent cascade with that of the energy flux into the elastic degrees of freedom of the dilute long-chain polymer solution. We propose a refined elastic length scale, $r_\\varepsilon$, which describes the effect of polymer elasticity on the turbulence energy cascade. Our experimental results agree excellently with this new energy ...

  6. Polymers as reference partitioning phase: polymer calibration for an analytically operational approach to quantify multimedia phase partitioning

    DEFF Research Database (Denmark)

    Gilbert, Dorothea; Witt, Gesine; Smedes, Foppe;

    2016-01-01

    Polymers are increasingly applied for the enrichment of hydrophobic organic chemicals (HOCs) from various types of samples and media in many analytical partitioning-based measuring techniques. We propose using polymers as a reference partitioning phase and introduce polymer-polymer partitioning...... as the basis for a deeper insight into partitioning differences of HOCs between polymers, calibrating analytical methods, and consistency checking of existing and calculation of new partition coefficients. Polymer-polymer partition coefficients were determined for polychlorinated biphenyls (PCBs), polycyclic...

  7. Polymer waveguide technology for flexible display applications

    Science.gov (United States)

    Okuda, Yuuto; Fujieda, Ichiro

    2012-03-01

    We consider applications of wave-guiding technologies for flexible displays. First, a flexible backlight can be constructed by guiding laser light through an optical fiber arranged in a spiral manner. The light leaks out via the grooves fabricated on the optical fiber. For uniform illumination, the probability of light extraction at each groove and the pitch of the grooves are adjusted. Second, a polymer waveguide with successive branches distributes the optical power from a laser to two-dimensional emission points on a plane. The division ratio at each branch is an important design parameter for uniform light output. At each branch and emission point, a mirror is placed for 90-degree optical path redirection. This constitutes a flexible backlight. Third, in a more technically demanding design, a mirror based on the micro-electro-mechanical systems technology scans a laser beam on the entrance surface of the waveguide and each emission point is addressed sequentially. An image can be displayed by intensity modulation of the laser light synchronized to this scanning action. The precision of the waveguide fabrication and the beam scanning accuracy would determine the display resolution. Finally, such a waveguide may be applied for concentrated photovoltaic applications. An array of lenses is stacked on the waveguide so that the optical power is focused on each mirror. The direction of the light propagation is reversed. Now the exit surface of the waveguide is coupled to solar cells. In all these cases, the polymer waveguide technology offers a cost advantage due to its feasibility for the roll-to-roll process.

  8. Understanding Polymer Properties through Imaging of Molecules.

    Science.gov (United States)

    Sheiko, Sergei

    2008-03-01

    The unique advantage of Scanning Probe Microscopy (SPM) is that it allows imaging of flexible polymer molecules, whose overall size and local curvature are below the optical resolution limit. The role of molecular visualization has grown to be especially profound with the synthesis of complex macromolecules whose structure is difficult to confirm using conventional techniques such as NMR and light scattering. This is especially true for molecules that are branched, heterogeneous, and polydisperse. Here, SPM images provide unambiguous proof of the molecular architecture along with accurate analysis of size, conformation, and ordering of molecules on surfaces. The unique advantage of SPM is that one obtains molecular dimensions in direct space. This offers more opportunities for statistical analysis including fractionation of molecules by size, branching topology, and chemical composition as well as sorting out the irrelevant species. Unlike molecular characterization of static molecules, it remains challenging to study molecules as they move and react on surfaces. We will discuss pioneering AFM studies of flowing monolayers one molecule at a time. Through use of AFM, the flow process was monitored over a broad range of length scales from the millimeter long precursor film all the way down to the movements of individual molecules within the film. Molecular imaging enabled independent measurements both the driving and frictional forces that control spreading rate. In these studies, one also discovered a new type of flow instability in polymer monolayers caused by flow-induced conformational transitions. Recently, molecular imaging has been successfully used to monitor adsorption-induced degradation of branched molecules. These experiments open an entirely new perspective in chemistry wherein the chemical bonds can be mechanically activated upon the physical contact of a macromolecule with a substrate. This research directly impacts coatings, lubrication, heterogeneous

  9. Origin of Symmetry Breaking and Confinement in Conducting Polymers with Ring Structures

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A model to describe the main features of conjugated polymers with ring structures, such as polythiophene and polypyrrole, is constructed. It is shown that the origin of the symmetry breaking and confinement of a soliton and anti-soliton pair is branch hopping in the polymer rings.

  10. Photochemical stability of electrochromic polymers and devices

    DEFF Research Database (Denmark)

    Jensen, Jacob; Madsen, Morten Vesterager; Krebs, Frederik C

    2013-01-01

    of the influence that the chemical constitution of the conjugated polymer backbone has on the photochemical stability. Based on changes in the UV-visible absorption and IR spectra, the polymers were categorized into two distinct groups, each with a separate degradation mechanism. During irradiation (1000 W m -2......, AM 1.5G) under ambient conditions the majority of the polymers degraded within 4-5 hours. Three polymers showed increased stability with degradation rates from 0.44 to 1.58% per hour measured as loss of absorption. Application of oxygen and UV barrier foils was found to drastically slow......The stability of fully printed flexible organic electrochromics based on 11 different conjugated polymers is explored from the fundamental chemical degradation level to the operational device level. The photochemical stability of the electrochromic polymers (ECPs) is studied enabling an analysis...

  11. Polymer-Based Carbon Monoxide Sensors

    Science.gov (United States)

    Homer, M. L.; Shevade, A. V.; Zhou, H.; Kisor, A. K.; Lara, L. M.; Yen, S.-P. S.; Ryan, M. A.

    2010-01-01

    Polymer-based sensors have been used primarily to detect volatile organics and inorganics; they are not usually used for smaller, gas phase molecules. We report the development and use of two types of polymer-based sensors for the detection of carbon monoxide. Further understanding of the experimental results is also obtained by performing molecular modeling studies to investigate the polymer-carbon monoxide interactions. The first type is a carbon-black-polymer composite that is comprised of a non-conducting polymer base that has been impregnated with carbon black to make it conducting. These chemiresistor sensors show good response to carbon monoxide but do not have a long lifetime. The second type of sensor has a non-conducting polymer base but includes both a porphyrin-functionalized polypyrrole and carbon black. These sensors show good, repeatable and reversible response to carbon monoxide at room temperature.

  12. Conductive polymer/superconductor bilayer structures

    International Nuclear Information System (INIS)

    The preparation of a hybrid conducting polymer/high-temperature superconductor device consisting of a polypyrrole-coated YBa2Cu3O7-∂ microbridge is reported. Electrochemical techniques are exploited to alter the oxidation state of the polymer and, in doing so, it is found for the first time that superconductivity can be modulated in a controllable and reproducible fashion by a polymer layer. Whereas the neutral (insulating) polypyrrole only slightly influences the electrical properties of the underlying YBa2Cu3O7-∂ film, the oxidized (conductive) polymer depresses Tc by up to 50K. In a similar fashion, the oxidation state of the polymer is found to modulate reversibly the magnitude of Jc, the superconducting critical current. Thus, a new type of molecular switch for controlling superconductivity is demonstrated. Electrochemical, resistance vs. temperature, conact resistance, atomic force microscopy and scanning electron microscopy measurements are utilized to explore the polymer/superconductor interactions

  13. Physical gelation in polymer-nanofiller systems

    Science.gov (United States)

    Xu, Di; Gersappe, Dilip

    2015-03-01

    Polymer gelation by physically crosslinking to sheet-like nanofillers was studied by Molecular Dynamics simulation. Nanofillers were modeled as rigid bodies of disk-like shapes and crosslinks were simulated by introducing a short-range attraction between the nanofillers and polymer chain ends. The structure, dynamics and mechanics of this polymer gel was studied as function of nanofiller volume fraction. Micelle like clusters were formed by polymers wrapping around nanofillers as its cores. These structures grow, with increased filler fraction, into fibrous structures. We observe the formation of a percolated nework of these fibrous structures, with ordered local structure but disordered globally, as we increase the filler fraction. The dynamics of polymers showed significant caging at intermediate time, in gel state, while the polymers move heterogeneously. Stress autocorrelation and elongation results were analyzed as a function of the nano-filler concentration.

  14. Velocity dependence of friction of confined polymers

    DEFF Research Database (Denmark)

    Sivebæk, Ion Marius; Samoilov, V.N.; Persson, B.N.J.

    2009-01-01

    We present molecular dynamics friction calculations for confined hydrocarbon solids with molecular lengths from 20 to 1400 carbon atoms. Two cases are considered: (a) polymer sliding against a hard substrate, and (b) polymer sliding on polymer. We discuss the velocity dependence of the frictional...... shear stress for both cases. In our simulations, the polymer films are very thin (approx. 3 nm), and the solid walls are connected to a thermostat at a short distance from the polymer slab. Under these circumstances we find that frictional heating effects are not important, and the effective temperature...... in the polymer film is always close to the thermostat temperature. In the first setup (a), for hydrocarbons with molecular lengths from 60 to 1400 carbon atoms, the shear stresses are nearly independent of molecular length, but for the shortest hydrocarbon C20H42 the frictional shear stress is lower. In all...

  15. Routing of individual polymers in designed patterns

    DEFF Research Database (Denmark)

    Knudsen, Jakob Bach; Liu, Lei; Kodal, Anne Louise Bank;

    2015-01-01

    Synthetic polymers are ubiquitous in the modern world, but our ability to exert control over the molecular conformation of individual polymers is very limited. In particular, although the programmable self-assembly of oligonucleotides and proteins into artificial nanostructures has been...... demonstrated, we currently lack the tools to handle other types of synthetic polymers individually and thus the ability to utilize and study their single-molecule properties. Here we show that synthetic polymer wires containing short oligonucleotides that extend from each repeat can be made to assemble...... into arbitrary routings. The wires, which can be more than 200 nm in length, are soft and bendable, and the DNA strands allow individual polymers to self-assemble into predesigned routings on both two- and three-dimensional DNA origami templates. The polymers are conjugated and potentially conducting, and could...

  16. Reversible Thermal Stiffening in Polymer Nanocomposites.

    Science.gov (United States)

    Senses, Erkan; Isherwood, Andrew; Akcora, Pinar

    2015-07-15

    Miscible polymer blends with different glass transition temperatures (Tg) are known to create confined interphases between glassy and mobile chains. Here, we show that nanoparticles adsorbed with a high-Tg polymer, poly(methyl methacrylate), and dispersed in a low-Tg matrix polymer, poly(ethylene oxide), exhibit a liquid-to-solid transition at temperatures above Tg's of both polymers. The mechanical adaptivity of nanocomposites to temperature underlies the existence of dynamically asymmetric bound layers on nanoparticles and more importantly reveals their impact on macroscopic mechanical response of composites. The unusual reversible stiffening behavior sets these materials apart from conventional polymer composites that soften upon heating. The presented stiffening mechanism in polymer nanocomposites can be used in applications for flexible electronics or mechanically induced actuators responding to environmental changes like temperature or magnetic fields.

  17. Characterizing the Polymer:Fullerene Intermolecular Interactions

    KAUST Repository

    Sweetnam, Sean

    2016-02-02

    Polymer:fullerene solar cells depend heavily on the electronic coupling of the polymer and fullerene molecular species from which they are composed. The intermolecular interaction between the polymer and fullerene tends to be strong in efficient photovoltaic systems, as evidenced by efficient charge transfer processes and by large changes in the energetics of the polymer and fullerene when they are molecularly mixed. Despite the clear presence of these strong intermolecular interactions between the polymer and fullerene, there is not a consensus on the nature of these interactions. In this work, we use a combination of Raman spectroscopy, charge transfer state absorption, and density functional theory calculations to show that the intermolecular interactions do not appear to be caused by ground state charge transfer between the polymer and fullerene. We conclude that these intermolecular interactions are primarily van der Waals in nature. © 2016 American Chemical Society.

  18. Entangled Polymer Melts in Extensional Flow

    DEFF Research Database (Denmark)

    Hengeller, Ludovica

    Many commercial materials derived from synthetic polymers exhibit a complex response under different processing operations such as fiber formation, injection moulding,film blowing, film casting or coatings. They can be processed both in the solid or in the melted state. Often they may contain two...... or more different polymers in addition to additives, fillers or solvents in order to modify the properties of the final product. Usually, it is also desired to improve the processability. For example the supplement of a high molecular weight component improves the stability in elongational flows....... Understanding the behaviour of polymer melts and solutions in complex non-linearflows is crucial for the design of polymeric materials and polymer processes. Through rheological characterization, in shear and extensional flow, of model polymer systems,i.e. narrow molar mass distribution polymer melts...

  19. Functional Films from Silica/Polymer Nanoparticles

    Directory of Open Access Journals (Sweden)

    Tânia Ribeiro

    2014-05-01

    Full Text Available High performance functional coatings, based on hybrid organic/inorganic materials, are being developed to combine the polymer flexibility and ease of processing with the mechanical properties and versatility of inorganic materials. By incorporating silica nanoparticles (SiNPs in the polymeric matrices, it is possible to obtain hybrid polymer films with increased tensile strength and impact resistance, without decreasing the flexural properties of the polymer matrix. The SiNPs can further be used as carriers to impart other functionalities (optical, etc. to the hybrid films. By using polymer-coated SiNPs, it is possible to reduce particle aggregation in the films and, thus, achieve more homogeneous distributions of the inorganic components and, therefore, better properties. On the other hand, by coating polymer particles with silica, one can create hierarchically structured materials, for example to obtain superhydrophobic coatings. In this review, we will cover the latest developments in films prepared from hybrid polymer/silica functional systems.

  20. Mechanically stiff, electrically conductive composites of polymers and carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Worsley, Marcus A.; Kucheyev, Sergei O.; Baumann, Theodore F.; Kuntz, Joshua D.; Satcher, Jr., Joe H.; Hamza, Alex V.

    2015-07-21

    Using SWNT-CA as scaffolds to fabricate stiff, highly conductive polymer (PDMS) composites. The SWNT-CA is immersing in a polymer resin to produce a SWNT-CA infiltrated with a polymer resin. The SWNT-CA infiltrated with a polymer resin is cured to produce the stiff and electrically conductive composite of carbon nanotube aerogel and polymer.

  1. MOLECULAR DESIGN OF FUNCTIONAL POLYMERS BASED ON UNIQUE PROPERTIES OF POLYMER CHAINS

    Institute of Scientific and Technical Information of China (English)

    Mikiharu Kamachi

    2000-01-01

    The inclusion complex formation of α-CD, β-CD, and γ-CD with various water-soluble polymers has been investigated, and the relationship between the chain cross-sectional areas of the polymers and the diameters of the cavities of cyclodextrins (molecular recognition) was found. Polyrotaxanes and tubular polymers were prepared on the basis of molecular recognition. Several kinds of polymers having tetraphenylporphyrin (TPP) and paramagnetic metallotetraphenylporphyrin (AgTPP, CuTPP, VOTPP or ZnTPP) have been prepared by radical polymerization of the corresponding monomers. Visible spectra of these polymers show hypochromism in the Soret bands of TPP moieties as compared with those of monomers. Polymer effects were observed in the magnetic behavior and oxygen adsorption of paramagnetic metallotetraphenylporphyrin moieties. Moreover, polymer effects on photophysical and photochemical behavior were found in the amphiphilic polymers covalently tethered with small amounts of zinc(Ⅱ)-tetraphenylporphyrin (ZnTPP).

  2. Fluoroalkylation of aryl ether perfluorocyclobutyl polymers

    OpenAIRE

    Ligon, Clark; Ameduri, Bruno; Boutevin, Bernard; Smith, Dennis

    2008-01-01

    Post functionalization of aryl ether perfluorocyclobutyl (PFCB) polymers with fluoroalkyl side chains was accomplished with Umemoto's FITS reagents. The fluoroalkylated PFCB polymers (20 % functionalized) showed increases in both hydrophobicity and oleophobicity. Static contact angle for hexadecane was increased after fluoroalkylation from 0° to greater than 30° for the two PFCB polymers tested. Increased oil repellency makes these materials potential candidates for various coatings applicati...

  3. Analysis of multi-layer polymer films

    Directory of Open Access Journals (Sweden)

    Paulette Guillory

    2009-04-01

    Full Text Available Polymer multi-layer films are used in a variety of industries. It is important both to the manufacturers of polymer films and to the industries using these films that the quality and composition be strictly controlled. The confocal analysis and high spatial resolution of Raman microscopy make this technique ideal for identifying the source and identity of defects and inclusions in polymer films.

  4. The Plasma Chemistry of Polymer Surfaces

    CERN Document Server

    Friedrich, Jö

    2012-01-01

    This book illustrates plasma properties, polymer characteristics, surface specifics, and how to purposefully combine plasma and polymer chemistry. In so doing, it covers plasma polymerization, surface functionalization, etching, crosslinking, and deposition of monotype functional-group-bearing plasma polymers. It explains different techniques and plasma types, such as pressure-pulsed, remote, low-wattage plasmas and plasma polymerization in liquids. Finally, among the numerous applications discussed are plasmas for chemical synthesis, industrial processes or the modification of membranes and p

  5. Assembly and performance of silicone polymer waveguides

    Science.gov (United States)

    Lostutter, Calob K.; Hodge, Malcolm H.; Marrapode, Thomas R.; Swatowski, Brandon W.; Weidner, W. Ken

    2016-03-01

    We report on the functionality and key performance properties of 50 μm x 50 μm flexible graded index silicone polymer waveguides. The materials show low optical propagation losses of manufacturing of polymer based optical printed wiring boards. The polymer waveguides are terminated with a passive direct fiber attach method. Fully MPO connectorized waveguide panels are realized and their optical performance properties assessed.

  6. Polymer-Ceramic Bionanocomposites for Dental Application

    OpenAIRE

    Jung-Hwan Lee; Hae-Won Kim; Seog-Jin Seo

    2016-01-01

    Multiphasic bionanocomposites have been highlighted in the biotechnology field since they have offered mechanical flexibility during operation. This interest has been increased mainly through polymer/ceramic/metal manipulation techniques and modifications in formulation. Recently, a number of studies on bionanocomposites have been examined due to their favorable mechanical properties and cellular activities when compared to the neat polymers or polymer blends. This paper critically reviews re...

  7. Enzymes as catalysts in polymer chemistry

    OpenAIRE

    Sinigoi, Loris

    2011-01-01

    The use of enzymes in synthetic chemistry is attracting the interest of many researchers thanks to their extraordinary efficiency under mild conditions, high stereo- regio- and chemoselectivity and low environmental impact. Their application in the field of polymer chemistry has provided new synthetic strategies for useful polymers. The advantages coming from the use of enzymes are mainly: i) the possibility to synthesize polymers with novel properties and difficult to produce by conventional...

  8. Asphaltenes-based polymer nano-composites

    Science.gov (United States)

    Bowen, III, Daniel E

    2013-12-17

    Inventive composite materials are provided. The composite is preferably a nano-composite, and comprises an asphaltene, or a mixture of asphaltenes, blended with a polymer. The polymer can be any polymer in need of altered properties, including those selected from the group consisting of epoxies, acrylics, urethanes, silicones, cyanoacrylates, vulcanized rubber, phenol-formaldehyde, melamine-formaldehyde, urea-formaldehyde, imides, esters, cyanate esters, allyl resins.

  9. Thermally activated solvent bonding of polymers

    OpenAIRE

    Ng, S H; Tjeung, R. T.; Z. F. Wang; Lu, A. C. W.; Rodriguez, I.; de Rooij, Nicolaas F.

    2010-01-01

    We present a thermally activated solvent bonding technique for the formation of embedded microstructures in polymer. It is based on the temperature dependent solubility of polymer in a liquid that is not a solvent at room temperature. With thermal activation, the liquid is transformed into a solvent of the polymer, creating a bonding capability through segmental or chain interdiffusion at the bonding interface. The technique has advantages over the more commonly used thermal bonding due to it...

  10. Biodegradable Polymers in Bone Tissue Engineering

    OpenAIRE

    Govaert, Leon E.; Smit, Theo H; Robert J. Kroeze; Helder, Marco N.

    2009-01-01

    The use ofdegradable polymers in medicine largely started around the mid 20th century with their initial use as in vivo resorbing sutures. Thorough knowledge on this topic as been gained since then and the potential applications for these polymers were, and still are, rapidly expanding. After improving the properties of lactic acid-based polymers, these were no longer studied only from a scientific point of view, but also for their use in bone surgery in the 1990s. Unfortunately, after implan...

  11. Galileo symmetries in polymer particle representation

    International Nuclear Information System (INIS)

    To illustrate the conceptual problems for the low-energy symmetries in the continuum of spacetime emerging from the discrete quantum geometry, Galileo symmetries are investigated in the polymer particle representation of a non-relativistic particle as a simple toy model. The complete Galileo transformations (translation, rotation and Galileo boost) are naturally defined in the polymer particle Hilbert space and Galileo symmetries are recovered with highly suppressed deviations in the low-energy regime from the underlying polymer particle description

  12. Experience With Polymer Thick Film Technology

    OpenAIRE

    Vesa Sortti; Raimo Hulkkonen; Eero Jarvinen

    1983-01-01

    The paper describes a user's experiences with polymer thick film resistor technology. The characteristics studied are resistance values and their distributing. Parameters affecting these characteristics are the material of the substrate, and the curing of the polymer resistor paste. The test conditions (temperature cycling, dip soldering, high temperature storaging) were chosen to simulate the environmental conditions, through which the polymer resistor circuits have to go during the assembly...

  13. Nanoscale molecularly imprinted polymers and method thereof

    Science.gov (United States)

    Hart, Bradley R.; Talley, Chad E.

    2008-06-10

    Nanoscale molecularly imprinted polymers (MIP) having polymer features wherein the size, shape and position are predetermined can be fabricated using an xy piezo stage mounted on an inverted microscope and a laser. Using an AMF controller, a solution containing polymer precursors and a photo initiator are positioned on the xy piezo and hit with a laser beam. The thickness of the polymeric features can be varied from a few nanometers to over a micron.

  14. Development of Polymer Materials for Combating Desertification

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Aiming respectively at the two problems in desertiflcation areas, namely water shortage and serious soil erosion, the polymer materials for combating desertiflcation may be classified as water absorbing-retaining polymers (WARPs) and sandy soil stabilizing polymers (SSSPs). Their further classifications and current researcfl situations were introduced. It is suggested that the major hindrancefor their wide appHcation is the high cost. The authors' newest research resuits on cutting cost and enhancing ef...

  15. High-Performance Polymers Having Low Melt Viscosities

    Science.gov (United States)

    Jensen, Brian J.

    2005-01-01

    High-performance polymers that have improved processing characteristics, and a method of making them, have been invented. One of the improved characteristics is low (relative to corresponding prior polymers) melt viscosities at given temperatures. This characteristic makes it possible to utilize such processes as resin-transfer molding and resin-film infusion and to perform autoclave processing at lower temperatures and/or pressures. Another improved characteristic is larger processing windows that is, longer times at low viscosities. Other improved characteristics include increased solubility of uncured polymer precursors that contain reactive groups, greater densities of cross-links in cured polymers, improved mechanical properties of the cured polymers, and greater resistance of the cured polymers to chemical attack. The invention is particularly applicable to poly(arylene ether)s [PAEs] and polyimides [PIs] that are useful as adhesives, matrices of composite materials, moldings, films, and coatings. PAEs and PIs synthesized according to the invention comprise mixtures of branched, linear, and star-shaped molecules. The monomers of these polymers can be capped with either reactive end groups to obtain thermosets or nonreactive end groups to obtain thermoplastics. The synthesis of a polymeric mixture according to the invention involves the use of a small amount of a trifunctional monomer. In the case of a PAE, the trifunctional monomer is a trihydroxy- containing compound for example, 1,3,5-trihydroxybenzene (THB). In the case of a PI, the trifunctional monomer is a triamine for example, triamino pyrimidine or melamine. In addition to the aforementioned trifunctional monomer, one uses the difunctional monomers of the conventional formulation of the polymer in question (see figure). In cases of nonreactive end caps, the polymeric mixtures of the invention have melt viscosities and melting temperatures lower than those of the corresponding linear polymers of equal

  16. Photoinitiated grafting of porous polymer monoliths and thermoplastic polymers for microfluidic devices

    Science.gov (United States)

    Frechet, Jean M. J.; Svec, Frantisek; Rohr, Thomas

    2008-10-07

    A microfluidic device preferably made of a thermoplastic polymer that includes a channel or a multiplicity of channels whose surfaces are modified by photografting. The device further includes a porous polymer monolith prepared via UV initiated polymerization within the channel, and functionalization of the pore surface of the monolith using photografting. Processes for making such surface modifications of thermoplastic polymers and porous polymer monoliths are set forth.

  17. Development of Polymer Blends in order to Toughening of Polymers: A review

    OpenAIRE

    Carlos Bruno Barreto Luna; Divânia Ferreira da Silva; Sabrina Kelly Trajano Basílio; Edcleide Maria Araújo; Adriano Lima da Silva; Ana Flavia Camara Bezerra

    2015-01-01

    Polymers are materials of large use in the various sectors of the world economy. The use of polymeric materials in daily life, instead of the classic materials has increased in recent decades. However, for certain structural applications polymers need to get tougher. One of the principal toughening techniques based on physical mixture of two or more components, forming the so-called polymer blends. The addition of rubber or not vulcanized in polymer compositions is reported in the literature ...

  18. High-density polymer microarrays: identifying synthetic polymers that control human embryonic stem cell growth.

    Science.gov (United States)

    Hansen, Anne; Mjoseng, Heidi K; Zhang, Rong; Kalloudis, Michail; Koutsos, Vasileios; de Sousa, Paul A; Bradley, Mark

    2014-06-01

    The fabrication of high-density polymer microarray is described, allowing the simultaneous and efficient evaluation of more than 7000 different polymers in a single-cellular-based screen. These high-density polymer arrays are applied in the search for synthetic substrates for hESCs culture. Up-scaling of the identified hit polymers enables long-term cellular cultivation and promoted successful stem-cell maintenance.

  19. Continuous polymer nanocoating on silica nanoparticles.

    Science.gov (United States)

    Chen, Dengyue; Singh, Dhananjay; Sirkar, Kamalesh K; Zhu, Jiangtao; Pfeffer, Robert

    2014-07-01

    Continuous polymer coating of nanoparticles is of interest in many industries such as pharmaceuticals, cosmetics, food, and electronics. Here we introduce a polymer coating/precipitation technique to achieve a uniform and controllable nanosize polymer coating on nanoparticles in a continuous manner. The utility of this technique is demonstrated by coating Aerosil silica nanoparticles (SNPs) of diameter 12 nm with the polymer Eudragit RL 100. Both hydrophilic and hydrophobic SNPs were successfully coated. After determining the cloud point of an acetone solution of the polymer containing a controlled amount of the nonsolvent water, the solid hollow fiber cooling crystallization (SHFCC) technique was employed to continuously coat SNPs with the polymer. A suspension of the SNPs in an acetone-water solution of the polymer containing a surfactant was pumped through the lumen of solid polypropylene hollow fibers in a SHFCC device; cold liquid was circulated on the shell side. Because of rapid cooling-induced supersaturation and heterogeneous nucleation, precipitated polymers will coat the nanoparticles. The thickness and morphology of the nanocoating and the particle size distribution of the coated SNPs were analyzed by scanning transmission electron microscopy (STEM) with electron energy loss spectroscopy (EELS), thermogravimetric analysis (TGA), and dynamic light scattering (DLS). Results indicate that uniformly polymer-coated SNPs can be obtained from the SHFCC device after suitable post-treatments. The technique is also easily scalable by increasing the number of hollow fibers in the SHFCC device. PMID:24903705

  20. ACOUSTIC EMISSION DURING STRETCHING OF POLYMERS

    Institute of Scientific and Technical Information of China (English)

    QIAN Renyuan; WANG Tiangui; SHEN Jingshu

    1983-01-01

    Acoustic emission has been studied for a wide range of polymers including amorphous glasses,semi-crystalline polymers, copolymers, polymer blends and a crosslinked rubber during the course of uni-axial stretching at room temperature. For non-crystalline polymers acoustic emission occurred in rather small number of events accompanied by crazing and micro-crack formation. Strong acoustic activity appeared during yielding and necking of crystalline polymers. Rather small number or none of acoustic bursts occurred during the initial stage of neck drawing but numerous strong bursts appeared when drawing proceeded approaching specimen break. Specimens of the same polymer but of different fabrication history may be reflected in their acoustic emission behavior. Acoustic emission during stretching crosslinked polybutadiene rubber was very weak but observable when the force-elongation curve started to deviate from the linear region. No Kaiser effect was observed for the rubber. Very strong and numerous acoustic emission was observed during stretching specimens of polymer blends.High impact resistant polymer modifications showed no sharp increase of acoustic activity before specimen break. So long as the polymer and conditions of specimen fabrication are the same quite reproducible acoustic emission behavior could be observed.

  1. Magnetic polymer nanospheres for anticancer drug targeting

    Energy Technology Data Exchange (ETDEWEB)

    JurIkova, A; Csach, K; Koneracka, M; Zavisova, V; Tomasovicova, N; Lancz, G; Kopcansky, P; Timko, M; Miskuf, J [Institute of Experimental Physics, Slovak Academy of Sciences, 040 01 Kosice (Slovakia); Muckova, M, E-mail: akasard@saske.s [Hameln rds a.s., 900 01 Modra (Slovakia)

    2010-01-01

    Poly(D,L-lactide-co-glycolide) polymer (PLGA) nanospheres loaded with biocom-patible magnetic fluid as a magnetic carrier and anticancer drug Taxol were prepared by the modified nanoprecipitation method with size of 200-250 nm in diameter. The PLGA polymer was utilized as a capsulation material due to its biodegradability and biocompatibility. Taxol as an important anticancer drug was chosen for its significant role against a wide range of tumours. Thermal properties of the drug-polymer system were characterized using thermal analysis methods. It was determined the solubility of Taxol in PLGA nanospheres. Magnetic properties investigated using SQUID magnetometry showed superparamagnetism of the prepared magnetic polymer nanospheres.

  2. Role of Polymer Loops in DNA Replication

    CERN Document Server

    Jun, S; Jun, Suckjoon; Bechhoefer, John

    2003-01-01

    Loop formation in long molecules occurs many places in nature, from solutions of carbon nanotubes to polymers inside a cell. In this article, we review theoretical studies of the static and dynamic properties of polymer loops. For example, long polymers must search many configurations to find a "target" binding site, while short polymers are stiff and resist bending. In between, there is an optimal loop size, which balances the entropy of long loops against the energetic cost of short loops. We show that such simple pictures of loop formation can explain several long-standing observations in DNA replication, quantitatively.

  3. Polymer escape from a confining potential

    Energy Technology Data Exchange (ETDEWEB)

    Mökkönen, Harri, E-mail: harri.mokkonen@aalto.fi [Department of Applied Physics and COMP CoE, Aalto University School of Science, P.O. Box 11100, FIN-00076 Aalto, Espoo (Finland); Faculty of Physical Sciences, University of Iceland, Reykjavík (Iceland); Ikonen, Timo [Department of Applied Physics and COMP CoE, Aalto University School of Science, P.O. Box 11100, FIN-00076 Aalto, Espoo (Finland); VTT Technical Research Centre of Finland, P.O. Box 1000, FI-02044 VTT (Finland); Jónsson, Hannes [Department of Applied Physics and COMP CoE, Aalto University School of Science, P.O. Box 11100, FIN-00076 Aalto, Espoo (Finland); Faculty of Physical Sciences, University of Iceland, Reykjavík (Iceland); Department of Physics, Brown University, Providence, Rhode Island 02912-1843 (United States); Ala-Nissila, Tapio [Department of Applied Physics and COMP CoE, Aalto University School of Science, P.O. Box 11100, FIN-00076 Aalto, Espoo (Finland); Department of Physics, Brown University, Providence, Rhode Island 02912-1843 (United States)

    2014-02-07

    The rate of escape of polymers from a two-dimensionally confining potential well has been evaluated using self-avoiding as well as ideal chain representations of varying length, up to 80 beads. Long timescale Langevin trajectories were calculated using the path integral hyperdynamics method to evaluate the escape rate. A minimum is found in the rate for self-avoiding polymers of intermediate length while the escape rate decreases monotonically with polymer length for ideal polymers. The increase in the rate for long, self-avoiding polymers is ascribed to crowding in the potential well which reduces the free energy escape barrier. An effective potential curve obtained using the centroid as an independent variable was evaluated by thermodynamic averaging and Kramers rate theory then applied to estimate the escape rate. While the qualitative features are well reproduced by this approach, it significantly overestimates the rate, especially for the longer polymers. The reason for this is illustrated by constructing a two-dimensional effective energy surface using the radius of gyration as well as the centroid as controlled variables. This shows that the description of a transition state dividing surface using only the centroid fails to confine the system to the region corresponding to the free energy barrier and this problem becomes more pronounced the longer the polymer is. A proper definition of a transition state for polymer escape needs to take into account the shape as well as the location of the polymer.

  4. SYNTHESIS AND CHARACTERIZATION OF TITANOCENE POLYMER DERIVATIVES

    Institute of Scientific and Technical Information of China (English)

    WANG Zhuting; SUN Shumen

    1988-01-01

    Titanocene polymer derivatives with potential antitumor properties were synthesized by interfacial condensation. The preformed polymers used are PAA (polyacrylic acid), CPSMA (1:1 alternating copolymer of styrene and maleic anhydride) and DVEMA (1:2 copolymer of divinyl ether and maleic anhydride). The ratio of practical and theoretical titanium content is 73.6%, 92.2% and 86.2% for PAA, CPSMA and DVEMA polymer derivatives respectively. The IR spectra of the polymer derivatives possess the characteristic absorptions of titanocene. XPS (X-ray photoelectron spectroscopy) of O1s and Ti2p3/2 supports the existence of Ti-O bonding.

  5. Dynamics of Hyperbranched Polymers under Confinement

    Science.gov (United States)

    Androulaki, Krystallenia; Chrissopoulou, Kiriaki; Anastasiadis, Spiros H.; Prevosto, Daniele; Labardi, Massimiliano

    2015-03-01

    The effect of severe confinement on the dynamics of three different generations of hyperbranched polyesters (Boltorns) is investigated by Dielectric Spectroscopy. The polymers are intercalated within the galleries of natural Na+-MMT, thus, forming 1nm polymer films confined between solid walls. The Tg's of the polymers determined by DSC show a clear dependence on the generation whereas the transition is completely suppressed when all the polymer chains are intercalated. The dynamic investigation of the bulk polymers reveals two sub-Tg processes, with similar behavior for the three polymers with the segmental relaxation observed above the Tg of each. For the nanocomposites, where all polymers are severely confined, the dynamics show significant differences compared to that of the bulk polymers. The sub-Tg processes are similar for the three generations but significantly faster and with weaker temperature dependence than those in the bulk. The segmental process appears at temperatures below the bulk polymer Tg, it exhibits an Arrhenius temperature dependence and shows differences for the three generations. A slow process that appears at higher temperatures is due to interfacial polarization. Co-financed by the EU and Greek funds through the Operational Program ``Education and Lifelong Learning'' of the NSRF-Research Funding Program: THALES-Investing in knowledge society through the Eur. Social Fund (MIS 377278) and COST Action MP0902-COINAPO.

  6. Nanopatterned polymer brushes: conformation, fabrication and applications

    Science.gov (United States)

    Yu, Qian; Ista, Linnea K.; Gu, Renpeng; Zauscher, Stefan; López, Gabriel P.

    2015-12-01

    Surfaces with end-grafted, nanopatterned polymer brushes that exhibit well-defined feature dimensions and controlled chemical and physical properties provide versatile platforms not only for investigation of nanoscale phenomena at biointerfaces, but also for the development of advanced devices relevant to biotechnology and electronics applications. In this review, we first give a brief introduction of scaling behavior of nanopatterned polymer brushes and then summarize recent progress in fabrication and application of nanopatterned polymer brushes. Specifically, we highlight applications of nanopatterned stimuli-responsive polymer brushes in the areas of biomedicine and biotechnology.

  7. Properties of Fiber Reinforced Polymer Concrete

    Directory of Open Access Journals (Sweden)

    Marinela Bărbuţă

    2008-01-01

    Full Text Available Polymer concrete is a composite material realized with resin and aggregates. In the present study the epoxy resin was used for binding the aggregates. In the composition were introduced near the fly ash, used as filler, the cellulose fibers. The mechanical characteristics such as compressive strength, flexural strength and split tensile strength of polymer concrete with fibers were investigated. The fiber percentage was constant, the epoxy resin and the filler dosages were varied. The cellulose fiber had not improved the mechanical characteristics of the polymer concrete in comparison to that of polymer concrete without cellulose fibers.

  8. Radiation resistance of nano carbon polymers

    International Nuclear Information System (INIS)

    Present article is devoted to radiation resistance of polymers containing nano carbon fillers. Therefore, the influence of ultraviolet and gamma-irradiation on structure and radiation resistance of nano carbon polymers was studied. The light resistance of polymers was studied under the light ageing conditions and the radiation resistance was studied under the static radiation ageing conditions. It is defined that injection of fillers in to the polymers and irradiation them by ultraviolet and gamma beams changes their mechanical and thermal properties and their light and radiation resistance as well.

  9. Light-Emitting Devices with Conjugated Polymers

    Directory of Open Access Journals (Sweden)

    Xian-Yu Deng

    2011-03-01

    Full Text Available This article introduces a previous study and tremendous progress in basic theoretical modeling, material developments and device engineering for polymer light-emitting devices (PLEDs.

  10. Nanocomposites Derived from Polymers and Inorganic Nanoparticles

    Directory of Open Access Journals (Sweden)

    In-Yup Jeon

    2010-06-01

    Full Text Available Polymers are considered to be good hosting matrices for composite materials because they can easily be tailored to yield a variety of bulk physical properties. Moreover, organic polymers generally have long-term stability and good processability. Inorganic nanoparticles possess outstanding optical, catalytic, electronic and magnetic properties, which are significantly different their bulk states. By combining the attractive functionalities of both components, nanocomposites derived from organic polymers and inorganic nanoparticles are expected to display synergistically improved properties. The potential applications of the resultant nanocomposites are various, e.g. automotive, aerospace, opto-electronics, etc. Here, we review recent progress in polymer-based inorganic nanoparticle composites.

  11. Synthetic polymers from readily available monosaccharides.

    Science.gov (United States)

    Galbis, J A; García-Martín, M G

    2010-01-01

    The low degradability of petroleum-based polymers and the massive use of these materials constitute a serious problem because of the environmental pollution that they can cause. Thus, sustained efforts have been extensively devoted to produce new polymers based on natural renewing resources and with higher degradability. Of the different natural sources, carbohydrates stand out as highly convenient raw materials because they are inexpensive, readily available, and provide great stereochemical diversity. New polymers, analogous to the more accredited technical polymers, but based on chiral monomers, have been synthesized from natural and available sugars. This chapter describes the potential of sugar-based monomers as precursors to a wide variety of macromolecular materials.

  12. Cyclic Polymer with Alternating Monomer Sequence.

    Science.gov (United States)

    Zhu, Wen; Li, Zi; Zhao, Youliang; Zhang, Ke

    2015-11-01

    Cyclic polymers with alternating monomer sequence are synthesized for the first time based on the ring-closure strategy. Well-defined telechelic alternating polymers are synthesized by reversible addition-fragmentation chain transfer polymerization by copolymerizing the electron acceptor monomer of N-benzylmaleimide and donor monomer of styrene with a feed ratio of 1 between them. The corresponding cyclic alternating polymers are then produced by the UV-induced Diels-Alder click reaction to ring-close the linear alternating polymer precursors under highly diluted reaction solution.

  13. Biodegradable synthetic polymers for tissue engineering

    Directory of Open Access Journals (Sweden)

    Gunatillake P. A.

    2003-05-01

    Full Text Available This paper reviews biodegradable synthetic polymers focusing on their potential in tissue engineering applications. The major classes of polymers are briefly discussed with regard to synthesis, properties and biodegradability, and known degradation modes and products are indicated based on studies reported in the literature. A vast majority of biodegradable polymers studied belongs to the polyester family, which includes polyglycolides and polylactides. Some disadvantages of these polymers in tissue engineering applications are their poor biocompatibility, release of acidic degradation products, poor processability and loss of mechanical properties very early during degradation. Other degradable polymers such as polyorthoesters, polyanhydrides, polyphosphazenes, and polyurethanes are also discussed and their advantages and disadvantages summarised. With advancements in tissue engineering it has become necessary to develop polymers that meet more demanding requirements. Recent work has focused on developing injectable polymer compositions based on poly (propylene fumarate and poly (anhydrides to meet these requirements in orthopaedic tissue engineering. Polyurethanes have received recent attention for development of degradable polymers because of their great potential in tailoring polymer structure to achieve mechanical properties and biodegradability to suit a variety of applications.

  14. Factors influencing the polymer-polymer adhesion- strength during two shot moulding

    DEFF Research Database (Denmark)

    Islam, Mohammad Aminul; Hansen, Hans Nørgaard; Tang, Peter Torben

    At the present state of two shot moulding, the adhesion strength of the two different polymers is an important issue. Many fascinating applications of two component or multi component polymer parts are restricted due to the weak interfacial adhesion of the polymers. A thorough understanding of the...

  15. Using Polydispersity in Polymer Grafted Nanoparticles for Tuning Morphology in Polymer Nanocomposites

    Science.gov (United States)

    Martin, Tyler; Jayaraman, Arthi

    2013-03-01

    Polymer nanocomposites, consisting of nanoscale additives in a polymer matrix, are used in many applications where high thermal and wear resistance is important e.g. automotive tires. To achieve uniform mechanical and thermal properties of the nanocomposite, the nanoparticles need to be well dispersed in the polymer matrix. One way to control the nanoparticle spatial organization in the polymer matrix is by grafting the nanoparticle surface with polymers that are chemically similar to the matrix polymer and tuning the effective interactions between the particles by simply tuning the grafting density, graft length, matrix length, particle size, filler concentration, and matrix density. In this study, we demonstrate that polydisperse polymer grafts can stabilize dispersions of polymer grafted nanoparticles in a polymer matrix in cases where monodisperse grafts would cause aggregation of particles. The change in the effective inter-particle interactions with increasing polydisersity is because of increased wetting of the grafted polymers by the matrix polymers. The implication that polydispersity can stabilize particle dispersions in matrix shows that it can be used as a design tool to program inter-particle interactions in a polymer matrix.

  16. Actinic-radiation curable polymers prepared from a reactive polymer, halogenated cyclic anhydride and glycidyl ester

    International Nuclear Information System (INIS)

    A novel class of photosensitive polymers are disclosed which are prepared by the reaction, preferably in the presence of a catalyst, of a reactive polymer, a halogenated cyclic anhydride and glycidyl ester of an alpha, beta-unsaturated carboxylic acid. These polymers are capable of undergoing vinyl-type polymerization when exposed to actinic radiation

  17. Cyclic behaviors of amorphous shape memory polymers.

    Science.gov (United States)

    Yu, Kai; Li, Hao; McClung, Amber J W; Tandon, Gyaneshwar P; Baur, Jeffery W; Qi, H Jerry

    2016-04-01

    Cyclic loading conditions are commonly encountered in the applications of shape memory polymers (SMPs), where the cyclic characteristics of the materials determine their performance during the service life, such as deformation resistance, shape recovery speed and shape recovery ratio. Recent studies indicate that in addition to the physical damage or some other irreversible softening effects, the viscoelastic nature could also be another possible reason for the degraded cyclic behavior of SMPs. In this paper, we explore in detail the influence of the viscoelastic properties on the cyclic tension and shape memory (SM) behavior of an epoxy based amorphous thermosetting polymer. Cyclic experiments were conducted first, which show that although the epoxy material does not have any visible damage or irreversible softening effect during deformation, it still exhibits obvious degradation in the cyclic tension and SM behaviors. A linear multi-branched model is utilized to assist in the prediction and understanding of the mechanical responses of amorphous SMPs. Parametric studies based on the applied model suggest that the shape memory performance can be improved by adjusting programming and recovery conditions, such as lowering the loading rate, increasing the programming temperature, and reducing the holding time. PMID:26924339

  18. Cyclic behaviors of amorphous shape memory polymers.

    Science.gov (United States)

    Yu, Kai; Li, Hao; McClung, Amber J W; Tandon, Gyaneshwar P; Baur, Jeffery W; Qi, H Jerry

    2016-04-01

    Cyclic loading conditions are commonly encountered in the applications of shape memory polymers (SMPs), where the cyclic characteristics of the materials determine their performance during the service life, such as deformation resistance, shape recovery speed and shape recovery ratio. Recent studies indicate that in addition to the physical damage or some other irreversible softening effects, the viscoelastic nature could also be another possible reason for the degraded cyclic behavior of SMPs. In this paper, we explore in detail the influence of the viscoelastic properties on the cyclic tension and shape memory (SM) behavior of an epoxy based amorphous thermosetting polymer. Cyclic experiments were conducted first, which show that although the epoxy material does not have any visible damage or irreversible softening effect during deformation, it still exhibits obvious degradation in the cyclic tension and SM behaviors. A linear multi-branched model is utilized to assist in the prediction and understanding of the mechanical responses of amorphous SMPs. Parametric studies based on the applied model suggest that the shape memory performance can be improved by adjusting programming and recovery conditions, such as lowering the loading rate, increasing the programming temperature, and reducing the holding time.

  19. Focus on polymer chemistry papers in Science China Chemistry of the year 2010

    Institute of Scientific and Technical Information of China (English)

    TIAN Ying; ZHU XiaoWen; CAO Yong

    2011-01-01

    The journal Science China Chemistry published 63 papers in polymer fields in 2010,leading to a percentage increase of 473% compared to the year 2008 and 70% to the year 2009,respectively(Figure 1).In this year,three polymer Special Topics were designed and published:Biomedical Polymer(Number 3)[1],Advances in Principles of Polymerization(Number 8)[2]and Highly Branched Polymers-Promising Architectural Macromolecules(Number 12)[3].Several high qualified papers were published and great achievements have been obtained in the year 2010.

  20. Nanotribological study of grafted polymer

    Science.gov (United States)

    Bouhacina, T.; Aimé, J. P.; Attias, A. J.

    1998-06-01

    The frictional forces between grafted layers, organosilanes and polymer, on silica and a nanotip have been investigated as a function of the tip velocity. From the interpretation of these results and one gets a step forward for more quantitative information. Les forces de friction entre des couches greffées sur silice et une nanopointe ont été étudiées en fonction de la vitesse de la pointe. À partir de l'interprétation de ces résultats on s'avance vers plus d'infor mations quantitatives.

  1. 3-dimensional polymer gel dosimetry

    International Nuclear Information System (INIS)

    Recently developed techniques in conformal radiotherapy demand special properties of radiation dosimeters. Polymer gel dosimeter evaluated by nuclear magnetic resonance (NMR) is promising tool which can be used for measuring rather complicated 3-dimensional dose distributions with required precision of ± 5 %. This system is based on radiation-induced polymerisation and cross-linking of acrylic monomers which are uniformly dispersed in aqueous gel. The formation of cross-linked polymers in the irradiated regions of the gel increases the NMR relaxation rates of neighbouring water protons. BANG-2 type polymer gel was prepared. The composition of gel dosimeter was as follows: 3 % N,N'-methylene-bisacrylamide, 3 % acrylic acid, 1 % sodium hydroxide, 5 % gelatine, and 88 % water, where all percentages are by weight. The dosimeters in glass vessels were homogeneously irradiated by 60Co gamma photons in a Gammacell 220 unit and by 4 MV, 6 MV and 18 MV X ray photons on Varian Clinac 600C and 2100 C linear accelerators by doses in the range of 0-50 Gy. Evaluation of dosimeters was performed on Siemens EXPERT 1 T and Siemens VISION 1,5 T scanners. Multi-echo CPMG sequence with 16 echoes was used for the evaluation of T2-relaxation times in irradiated gel dosimeters. The dependence of 1/T2 response of dosimeters was studied on following factors: absorbed dose, energy of applied radiation, temperature during NMR evaluation, time since irradiation to NMR evaluation and strength of the magnetic field. An exponential dependence of 1/T2 response on absorbed dose in the range of 0-50 Gy was observed, in the range 0-10 Gy the data could be fitted by a linear function. There was observed no dependence of 1/T2 response on: energy (for three different photon energies used in this study), strength of magnetic field of NMR scanner, time from irradiation of the dosimeters to NMR evaluation. Increase of gel dosimeter 1/T2 response with the decrease of the temperature during NMR evaluation

  2. Enhanced flame retardant polymer nanocomposites

    OpenAIRE

    Elbasuney, Sherif

    2013-01-01

    Fire is a continuous threat to life and property. The total annual UK fire loss is estimated to be 0.25% of its gross domestic product (GDP) (Goddard, 1995). According to fire statistics, more than 12 million fires break out every year in the United States, Europe, Russia, and China killing about 166,000 people and injuring several hundreds of thousands (Morgan and Wilkie, 2007). Polymers which take up 80% of the organic chemical industry, are known for their high flammability with the produc...

  3. Polymers for electronic & photonic application

    CERN Document Server

    Wong, C P

    2013-01-01

    The most recent advances in the use of polymeric materials by the electronic industry can be found in Polymers for Electronic and Photonic Applications. This bookprovides in-depth coverage of photoresis for micro-lithography, microelectronic encapsulants and packaging, insulators, dielectrics for multichip packaging,electronic and photonic applications of polymeric materials, among many other topics. Intended for engineers and scientists who design, process, and manufacturemicroelectronic components, this book will also prove useful for hybrid and systems packaging managers who want to be info

  4. RAFT polymers for protein recognition

    Directory of Open Access Journals (Sweden)

    Alan F. Tominey

    2010-06-01

    Full Text Available A new family of linear polymers with pronounced affinity for arginine- and lysine-rich proteins has been created. To this end, N-isopropylacrylamide (NIPAM was copolymerized in water with a binding monomer and a hydrophobic comonomer using a living radical polymerization (RAFT. The resulting copolymers were water-soluble and displayed narrow polydispersities. They formed tight complexes with basic proteins depending on the nature and amount of the binding monomer as well as on the choice of the added hydrophobic comonomer.

  5. Recycling of polymers by pyrolysis

    OpenAIRE

    Kaminsky, W.

    1993-01-01

    The pyrolysis of plastic waste, scrap tires and other polymeric materials in a fluidized bed has been carried out based on a scale up program (laboratory plants 70 g/h, 500 g/h, 3000 g/h, and pilot plant 20-50 kg/h). The fluidized bed shows short residence times and high heat and mass transfers, and is heated indirectly up to 600 - 800°C. In the case of poly(methylmethacrylate) (PMMA) or polystyrene as feedstock up to 97 wt.% of the monomer can be recovered. Other polymers give a more unspeci...

  6. Surface dynamics of polymer films

    International Nuclear Information System (INIS)

    The dynamics of supported polymer films were studied by probing the surface height fluctuations as a function of lateral length scale using x-ray photon correlation spectroscopy. Measurements were performed on polystyrene (PS) films of thicknesses varying from 84 to 333 nm at temperatures above the PS glass transition temperature. Within a range of wave vectors spanning 10-3 to 10-2 nm-1, good agreement is found between the measured surface dynamics and the theory of overdamped thermal capillary waves on thin films. Quantitatively, the data can be accounted for using the viscosity of bulk PS

  7. Structured fluids polymers, colloids, surfactants

    CERN Document Server

    Witten, Thomas A

    2010-01-01

    Over the last thirty years, the study of liquids containing polymers, surfactants, or colloidal particles has developed from a loose assembly of facts into a coherent discipline with substantial predictive power. These liquids expand our conception of what condensed matter can do. Such structured-fluid phenomena dominate the physical environment within living cells. This book teaches how to think of these fluids from a unified point of view showing the far-reaching effects ofthermal fluctuations in producing forces and motions. Keeping mathematics to a minimum, the book seeks the simplest expl

  8. Forces between asymmetric polymer brushes

    OpenAIRE

    Shim, D.F.K.; Cates, M. E.

    1990-01-01

    We study the equilibrium compression of asymmetric polymer brushes grafted on flat plates, under athermal and theta solvent conditions, using a lattice self-consistent field (SCF) approach. We find that the separation d between two plates coated asymmetrically with brushes of type 1 and 2, as a function of the force F, obeys the "bisection rule", d(F) = (d1(F) + d 2(F)) /2 where d1(F)and d 2(F) are the corresponding separations for the symmetric brushes of type 1 and 2 respectively.The bisect...

  9. Release characteristics of selected carbon nanotube polymer composites

    Science.gov (United States)

    Multi-walled carbon nanotubes (MWCNTs) are commonly used in polymer formulations to improve strength, conductivity, and other attributes. A developing concern is the potential for carbon nanotube polymer nanocomposites to release nanoparticles into the environment as the polymer ...

  10. Synthesis and Electronic Properties of Transition Metal Containing Polymers

    Institute of Scientific and Technical Information of China (English)

    Wai Kin Chan

    2000-01-01

    @@ 1. Introduction Since the discovery of the first organic light emitting polymer in 1991, research in this area has been mainly focused on conjugated organic polymers. The use of polymer metal complexes for electroluminescence applications has received relatively few attention.

  11. Restructuring polymers via nanoconfinement and subsequent release

    Directory of Open Access Journals (Sweden)

    Alan E. Tonelli

    2012-08-01

    Full Text Available During the past several years my students and I have been utilizing certain small-molecule hosts to create nanostructured polymers. This is accomplished by first forming noncovalently bonded inclusion complexes (ICs between these small-molecule hosts and guest polymers, followed by the careful removal of the host crystalline lattice to obtain a coalesced bulk polymer. We have repeatedly observed that such coalesced polymer samples behave distinctly from those produced from their solutions or melts. Coalesced amorphous homopolymers exhibit higher glass-transition temperatures, while crystallizable homopolymers coalesced from their ICs display higher melting and crystallization temperatures, and sometimes different crystalline polymorphs. When ICs are formed with block copolymers or with two or more different homopolymers, the resulting coalesced samples can exhibit intimate mixing between the copolymer blocks, or between entire homopolymer chains. Each of the distinct behaviors observed for polymers coalesced from their ICs is a consequence of the structural organization of the polymer–host-ICs. Polymer chains in host-IC crystals are confined to occupy narrow channels (diameter ~0.5–1.0 nm formed by the small-molecule hosts around the included guest polymers during IC crystallization. This results in the separation and high extension of the included guest polymer chains, which leads, following the careful removal of the host molecule lattice, to unique behaviors for the bulk coalesced polymer samples. Apparently, substantial degrees of the extended and unentangled natures of the IC-included chains are retained upon coalescence. In this review we summarize the behaviors and uses of coalesced polymers, and attempt to draw conclusions on the relationship between their behavior and the organization/structures/conformations of the constituent polymer chains achieved upon coalescence from their ICs.

  12. Approaches to blue light emitting polymers

    International Nuclear Information System (INIS)

    Blue-light emitting polymers are important for full colour displays. Blue- light emitting polymers, such as poly(fluorene)s have been reported, but tend to be soluble in the conjugated form. The aim of the project was to produce insoluble polymers, prepared via processible soluble precursor polymers, so that multilayer devices could be easily fabricated. Multilayer devices are often required for more efficient light emission. The target materials were derivatives of poly(p-phenylenevinylene) (PPV), a green-yellow emitting polymer. To blue shift the emission of PPV, bulky substituents, namely chloro, phenyl and alkyl, were attached to the vinylic linkage. These bulky substituents were incorporated to introduce steric interactions between the side group and the backbone phenyl protons, to shorten the effective conjugation length and increase the HOMO-LUMO energy gap. Chloro substituents quenched the fluorescence. Phenyl substituents resulted in highly conjugated precursor polymers with low molecular weights, showing blue- green to green emission in the conjugated form. Alkyl substituted PPV derivatives, prepared via chloro or xanthate precursors, were blue-light emitting conjugated polymers, which were electroluminescent in ITO/polymer/AI devices. The PL quantum yields were found to be up to 38%. The incorporation of electron withdrawing groups into the polymers was attempted, to lower the barrier to electron injection. Chloro groups quenched fluorescence and methylsulfone substituents resulted in insoluble polymers, probably due to cross-linking. However a copolymer containing methylsulfone electron withdrawing groups could be prepared. Phenylsulfone substituents were found to give fluorescent polymers which were soluble in the precursor form. (author)

  13. Morphology diversity of injection moulded polymer composites

    Directory of Open Access Journals (Sweden)

    M. Bilewicz

    2006-02-01

    Full Text Available Purpose: This work was performed in the aim of exploring non-conventional injection moulding technique and to study the effect of processing thermomechanical treatment on the morphology and properties of polymer-polymer composites.Design/methodology/approach: Multilayered highly oriented skin regions induced by high shearing of the melt were obtained during non-conventional injection moulding process. Structure development has been observed in the polarized light microscope and by scanning electron microscopy. The fracture energy has been calculated from notched bar specimens.Findings: The processing variables (melt temperature, stroke time and number are determinant of the fracture energy of the neat PP. Higher setting of these processing variables gives enhanced fracture energy (25% higher. Immiscible polymer blend of PP/PC processed by melt manipulation techniques show improved fracture toughness compared to neat PP. Addition of MAP to PP/PC did not affect the fracture energy for low setting of the processing variables, but significantly decreased it for high adjustments. The fracture energy of nanoclay reinforced PP is the double of the neat PP, for both melt temperature settings. Lower values of fracture energy have been obtained for polymer-polymer composite of PP/PC reinforced with nanoparticles (3-fold lower.Research limitations/implications: Further work contains research of different materials’ ratio, as well different polymer-polymer compositions (e.g., PP/PS and PP/LCP. Other mechanical properties will be assessed.Practical implications: The improvement of mechanical response is sharply apparent by use of SCORIM technique and by the use of nanoparticles reinforcement.Originality/value: This polymer processing technology is promising route for morphology manipulation and improvement on the mechanical properties of polymer systems. Research studies on processing-structure-properties relationships of polymer-polymer composites and

  14. Les mélanges de polymères incompatibles Incompatible Polymer Mixtures

    Directory of Open Access Journals (Sweden)

    Serpe G.

    2006-11-01

    Full Text Available Les mélanges de polymères thermoplastiques font actuellement l'objet d'un effort considérable de recherche et de développement. Cette synthèse bibliographique concerne principalement les mélanges mécaniques de polymères incompatibles à l'état fondu. Ceux-ci ont une morphologie hétérogène qui dépend des conditions de mise en oeuvre autant que de la nature des constituants. De plus, pour ce type de matériaux, la nature de l'interface joue un rôle déterminant sur la formation de la morphologie hétérogène et donc sur les propriétés du produit final. D'autre part un problème important réside dans la stabilité des mélanges réalisés. L'ajout d'une faible quantité d'agent tensioactif de type copolymère séquencé, ou greffé, ou la modification chimique des constituants (greffage ou réticulation par exemple permet, dans certains cas d'améliorer très sensiblement les propriétés des mélanges en augmentant l'adhérence entre les phases immiscibles. L'ensemble de ces considérations permettent la réalisation industrielle de nouveaux matériaux polymères aux caractéristiques spécifiques. Thermoplastic polymer mixtures are currently the subject of considerable research and development efforts. This bibliographic synthesis deals mainly with melt blending process of incompatible polymers. These blends have a heterogeneous morphology that depends on the processing conditions as much as on the chemical structure of the componants. Likewise, for these materials the nature of the interface plays a decisive role on the formation of the heterogeneous morphology and hence on the properties on the end product. Furthermore, an important problem is to stabilize the morphology of the blends. Adding a small amount of surfactant of the sequenced of grafted copolymer type or, else, the chemical reaction of the constituents (e. g. grafting or branching during processing are ways in some cases of considerably improving the properties of

  15. Parallel Synthesis of photoluminescent π-conjugated polymers by polymer reactions of an organotitanium polymer with a titanacyclopentadiene unit.

    Science.gov (United States)

    Matsumura, Yoshimasa; Fukuda, Katsura; Inagi, Shinsuke; Tomita, Ikuyoshi

    2015-04-01

    A regioregular organometallic polymer with titanacyclopentadiene unit, obtained by the reaction of a 2,7-diethynylfluorene derivative and a low-valent titanium complex, is subjected to the reaction with three kinds of electrophiles (i.e., sulfur monochloride, hydrochloric acid, and dichlorophenylphosphine) to give π-conjugated polymers possessing both fluorene and building blocks originated from the transformation of the titanacycles in the main chain. For example, a phosphole-containing polymer whose number-average molecular weight is estimated as 5000 is obtained in 50% yield. The obtained thiophene, butadiene, and phosphole-containing polymers exhibit efficient photoluminescence (PL) with emission colors of blue, green, and yellow, respectively. For example, the phosphole-containing polymer exhibits yellow PL with an emission maximum (Emax ) of 533 nm and a quantum yield (Φ) of 0.37.

  16. Preparation and degradation mechanisms of biodegradable polymer: a review

    Science.gov (United States)

    Zeng, S. H.; Duan, P. P.; Shen, M. X.; Xue, Y. J.; Wang, Z. Y.

    2016-07-01

    Polymers are difficult to degrade completely in Nature, and their catabolites may pollute the environment. In recent years, biodegradable polymers have become the hot topic in people's daily life with increasing interest, and a controllable polymer biodegradation is one of the most important directions for future polymer science. This article presents the main preparation methods for biodegradable polymers and discusses their degradation mechanisms, the biodegradable factors, recent researches and their applications. The future researches of biodegradable polymers are also put forward.

  17. Polymer gratings based on photopolymerization for low-order distributed feedback polymer lasers

    Institute of Scientific and Technical Information of China (English)

    Xuanke Zhao; Qingwu Zhao; Qinghua Zhang

    2008-01-01

    Novel polymer distributed feedback(DFB)gratings are fabricated based on photopolymerization to reduce lasing threshold of polymer lasers.A photopolymer formulation sensitive to 355-nm ultraviolet(UV)light is proposed for the fabrication of polymer gratings and it can be used to form polymer films by spin-coating process.A very low surface-relief depth ranging from 12.5 to about 1.0 nm has been demonstrated with a refractive-index modulation of about 0.012.The experimental results indicate that such polymer gratings have promising potentials for the fabrication of low-order DFB organic semiconductor lasers.

  18. Thiophene in Conducting Polymers: Synthesis of Poly(thiophene)s and Other Conjugated Polymers Containing Thiophenes, for Application in Polymer Solar Cells

    DEFF Research Database (Denmark)

    Livi, Francesco; Carlé, Jon Eggert; Bundgaard, Eva

    2015-01-01

    Conducting polymers based on thiophene are described. The polymers include poly(thiophene) with and without side-chains and other conjugated polymers in general, based on thiophene. The synthesis and characteristics of the polymers are described along with the application of these as light-absorb...

  19. The two dimensional shapes of simple three and four junction ideal comb polymers

    Science.gov (United States)

    de Regt, Robin; Bishop, Marvin; Barillas, Adam J.; Borgeson, Tylor; von Ferber, Christian

    2016-09-01

    We redesign and apply a scheme originally proposed by Wei (1995) [2,3] to produce numerical shape parameters with high precision for arbitrary tree-branched polymers based on their Kirchhoff matrix eigenvalue spectrum. This algorithm and a Monte Carlo growth method on square and triangular lattices are employed to investigate the shapes of ideal three and four junction two dimensional comb polymers. We find that the extrapolated values obtained by all of these methods are in excellent agreement with each other and the available theory. We confirm that polymers with a complete set of interior branches display a more circular shape.

  20. Record high hole mobility in polymer semiconductors via side-chain engineering.

    Science.gov (United States)

    Kang, Il; Yun, Hui-Jun; Chung, Dae Sung; Kwon, Soon-Ki; Kim, Yun-Hi

    2013-10-01

    Charge carrier mobility is still the most challenging issue that should be overcome to realize everyday organic electronics in the near future. In this Communication, we show that introducing smart side-chain engineering to polymer semiconductors can facilitate intermolecular electronic communication. Two new polymers, P-29-DPPDBTE and P-29-DPPDTSE, which consist of a highly conductive diketopyrrolopyrrole backbone and an extended branching-position-adjusted side chain, showed unprecedented record high hole mobility of 12 cm(2)/(V·s). From photophysical and structural studies, we found that moving the branching position of the side chain away from the backbone of these polymers resulted in increased intermolecular interactions with extremely short π-π stacking distances, without compromising solubility of the polymers. As a result, high hole mobility could be achieved even in devices fabricated using the polymers at room temperature. PMID:24053786