Relevant bibliographies by topics / Polystyre

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Polystyre'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Polystyre"

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Masruroh, D. J. D. H. Djoko, Lalu A. Didik, Eka Rahmawati, Masdiana Pagaga, Abdurrouf, and S. P. Sakti. "Solvent Effect on Morphology of Polystyrene Coating and their Role to Improvement for Biomolecule Immobilization in Application of QCM Based Biosensor." Applied Mechanics and Materials 530-531 (February 2014): 54–57. http://dx.doi.org/10.4028/www.scientific.net/amm.530-531.54.

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This research is focused on the synthesis of a polystiren layer for biosensors based on a Quartz Crystal Microbalance sensor (QCM) to immobilize the biomolecule. The polystyrene thin film was deposited by means of spin coating method with various solvents, such as chloroform, toluene, xylene, and tetrahydrofuran (THF), containing a 3% polystyrene solution by mass. The morphologies of the polystyrene layers were observed via SEM/EDx. The polystyrene surface coated using chloroform as the solvent has a rougher morphology and the largest diameter pores compared with the other solvents. The result show the polystyrene surface coating produced with chloroform caused a higher frequency change, which resulted in the binding of a wider range of biomolecules.
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Ford, Warren T., Alanta L. Lary, and Thomas H. Mourey. "Addition of Polystyryl Radicals from TEMPO-Terminated Polystyrene to C60." Macromolecules 34, no. 17 (August 2001): 5819–26. http://dx.doi.org/10.1021/ma0020990.

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Donchak, Volodymyr, and Khrystyna Harhay. "Synthesis of fluorinated polystyrene." Chemistry & Chemical Technology 2, no. 1 (March 15, 2008): 11–14. http://dx.doi.org/10.23939/chcht02.01.011.

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Acylation of polystyrene with trifluoroacetic anhydride in a solution of aprotonic solvents, namely 1,2-dichloroethane, chlorobenzene at the presence of Lewis acid as catalyst results in obtaining of fluorinated polystyrene, which posses trifluoroacetic fragments in benzoic rings, preferably in position 4. In order to achieve a total substitution of benzene rings in polystyrene macromolecules, the ratio polystyrene : trifluoroacetic anhydride : AlCl3 must be at least 1:10:2.2 mol correspondingly
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Alahmad, Waed. "Sunlight Photodegradable Polystyrene-TiO2/SiO2 Composite." Chemistry & Chemical Technology 13, no. 2 (June 10, 2019): 190–97. http://dx.doi.org/10.23939/chcht13.02.190.

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Lee, Jong-Su, Hyun-Seok Shin, Jin-Woo Seok, Gyu-Wan Jang, and Yeong-Hwan Beag. "Surface Modification of Polystyrene (PS) by Atmospheric Pressure Plasma." Journal of the Korean Vacuum Society 18, no. 1 (January 30, 2009): 1–8. http://dx.doi.org/10.5757/jkvs.2009.18.1.001.

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Sytnik, O. U. "Polymer composite based on polystyrene containing GdF3 nanoparticles." Functional materials 20, no. 2 (June 25, 2013): 243–47. http://dx.doi.org/10.15407/fm20.02.243.

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Zhmurin, P. N. "Polystyrene-based plastic scintillator for n/γ -discrimination." Functional materials 21, no. 3 (September 30, 2014): 282–89. http://dx.doi.org/10.15407/fm21.03.282.

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Weidner, C. H., and T. E. Long. "Synthesis and characterization of 3-aryl-2-(polystyryl)cyclopropenones via cyclopropenium ion substitution on polystyrene." Journal of Polymer Science Part A: Polymer Chemistry 33, no. 1 (January 15, 1995): 1–6. http://dx.doi.org/10.1002/pola.1995.080330101.

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Kim, Doo-Hwan, and Sang-Woog Ryu. "Synthesis and Ionic Conductivity of Polystyrene Derivative Containing Cyclic Carbonate." Journal of the Korean Electrochemical Society 18, no. 1 (February 28, 2015): 1–6. http://dx.doi.org/10.5229/jkes.2015.18.1.1.

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Kim, Jae Seon, and Chung Kun Song. "Performance Improvement of TIPS-pentacene OTFTs by blending with Polystyrene." Journal of the Institute of Electronics and Information Engineers 50, no. 7 (July 25, 2013): 96–101. http://dx.doi.org/10.5573/ieek.2013.50.7.096.

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Dissertations / Theses on the topic "Polystyre"

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Pukančíková, Andrea. "Praktické aspekty blokové polymerace styrenu." Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2010. http://www.nusl.cz/ntk/nusl-216622.

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The diploma thesis deals with radical bulk polymerization of styrene. Recent knowledges about mono- and multifunctional initiators of radical polymerization and coordination polymerization of styrene with metalocene initiators are summarized in theoretical part. Experimental part of diploma thesis is focused on relationship between polymerization conditions and conversion, molecular mass and distribution of molecular mass. Experiments carried out with monofunctional initiators (dibenzoylperoxide, dilauroylperoxide, tert-butylperbenzoate) and with bifunctional initiators (Luperox 101 and Luperox 256). Polymerizations took place at temperatures from 80 to 134 °C, reaction time was from 1 to 24 hours, and pressure was 100 and 500 kPa. Conversion of monomer was determined by gravimetry and infrared spectroscopy. Molecular mass and indexes of polydisperzity were measured by gel permeation chromatography in solutions of polystyrene with tetrahydrofurane at temperature 23 °C.
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Dohnalová, Tea. "Skleněný pastýř." Master's thesis, Vysoké učení technické v Brně. Fakulta výtvarných umění, 2019. http://www.nusl.cz/ntk/nusl-396117.

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The topic of my thesis are menhirs. Specifically, the largest Czech menhir known as the Stone Shepherd (3200 cm). The aim of this work was to transfer the exact shape and size of this megalith and materialize it here in Brno. This goal required the use of many procedures. At the beginning there was a photo shoot, then a 3D program, 3D program editing, and slicing into contour lines. Then I projected the menhir on a wall in real size and traced it to polystyrene boards. The next step was to cut out all 104 plates on a band saw and I could go to gluing and folding the whole object. The final step was to paint the object in white. The result is a simple and clean polystyrene object. I did not cover the contour lines - I present the object in the most direct form possible. The styrofoam megalith, despite its size, is a sculpture in the interior. Ideally, I would create an installation that would create a separate, isolated space for the object.
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Mailhot-Jensen, Bénédicte. "Etude des mécanismes de photooxydation du polystyrène, du polyacrylonitrile et du polystyrene-co-acrylonitrile." Clermont-Ferrand 2, 1993. http://www.theses.fr/1993CLF21502.

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Les comportements photochimiques du polystyrène, du polyacrylonitrile et du poly(styrene-co-acrylonitrile), sous irradiations a courte longueur d'onde (egale a 254 nm) et a grandes longueurs d'onde (superieures ou egales a 300 nm), ont été étudiés. Différentes techniques d'identification des photoproduits formes lors de l'irradiation des polymères sous forme de films solides ont été utilisées: spectroscopies irtf et uv-visible, chromatographie hplc. D'autres méthodes, permettant de transformer spécifiquement les photoproduits, ont été associées a ces techniques analytiques: traitements chimiques (sf#4,nh#3,hcl,ch#3oh,h#2o) et traitements physiques (photolyse, thermolyse et thermooxydation). L'identification des photoproduits et la caractérisation de leur stabilité thermique et photochimique ont permis d'établir le mécanisme de photooxydation de chacun des trois polymères étudiés
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Merche, Delphine. "Synthèse et caractérisation de couches de polystyrène et de polystyrène sulfoné obtenues par polymérisation-plasma à pression (sub)-atmosphérique." Doctoral thesis, Universite Libre de Bruxelles, 2011. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209871.

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Lors de ce travail, de fins films de polystyrène ont été déposés dans la post-décharge d’une torche plasma atmosphérique commerciale, mais aussi dans la décharge d’une DBD (Décharge à Barrière Diélectrique), conçue et développée par nos soins au laboratoire. Une DBD est un procédé permettant d’obtenir des plasmas froids à pression atmosphérique.

Nos résultats ont montré que la DBD permettait d’obtenir des films de polystyrène de meilleure qualité (degré d’oxydation moindre…) qu’avec la torche commerciale en raison de l’atmosphère contrôlée de l’enceinte DBD. Les films sont déposés en présence d’un gaz porteur (Ar ou He dans la DBD). Nous avons pu mettre en évidence l’influence de la nature de ce gaz porteur sur la structure des films (degré de branchement, et de réticulation des films et de préservation des cycles aromatiques de la molécule de départ).

Les dépôts de polystyrène sulfoné ont été synthétisés dans la DBD en une seule étape, par « copolymérisation » de deux précurseurs (styrène et acide trifluorométhane sulfonique) injectés simultanément dans la décharge. Ces membranes pourraient servir d’électrolyte dans les piles à combustibles miniaturisées de type PEMFC (« Polymer Electrolyte Membrane Fuel Cell »), utilisant de l’hydrogène ou du méthanol et ce pour des applications portables.

L’acide trifluorométhane sulfonique permet le greffage de groupements sulfoniques échangeurs d’ions (nécessaires pour la conductivité de la membrane) sur le squelette de polystyrène.

La complémentarité des différentes techniques spectroscopiques utilisées -Spectroscopie des Photoélectrons X (XPS), Infra-Rouge à Transformée de Fourier (FTIR), Spectroscopie des Ions Secondaires (SIMS) statique et dynamique- ont montré que les groupements acides sulfoniques (bien préservés dans la décharge à pression sub-atmosphérique) étaient bien greffés dans la matrice de polystyrène, et ce sur toute l’épaisseur de la membrane. L’influence des paramètres (température de l’acide, tension appliquée entre les électrodes, nature du gaz porteur…) sur la quantité de groupements ionisables greffés, sur la vitesse de dépôt et aussi sur la morphologie des films a été étudiée respectivement par XPS et par microscopie.

En plus des dépôts sur substrats usuels (Si, acier…) utilisés pour les caractérisations chimiques, nous avons synthétisé les films directement sur des électrodes de carbone enrichies en platine.

Nous avons déposé le catalyseur à partir d’une solution colloïdale de platine nébulisée dans la post-décharge d’une torche plasma atmosphérique sur des couches de carbones poreuse et sur du carbone vitreux (utilisé comme modèle pour le profilage par SIMS dynamique) dans différentes configurations et ce pour différents paramètres afin de constituer des électrodes servant de substrat pour l’adhésion de la membrane-plasma pour des perspectives d’assemblage membrane-électrodes pour PAC. /

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Doctorat en Sciences
info:eu-repo/semantics/nonPublished

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Svačina, Zdeněk. "Příprava syndiotaktického polystyrenu pomocí monocyklopentadienylových komplexů titanu." Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2008. http://www.nusl.cz/ntk/nusl-216371.

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A series of four novel halosilylsubstitued monocyclopentadienyl titanium complexes; [Si(CH3)2FCp]TiCl3 – FSiTTC, [Si(CH3)F2Cp]TiCl3 F2SiTTC, [Si(CH3)Cl2Cp]TiCl3 - Cl2SiTTC, [Si(CH3)2ClCp]TiCl3 - ClSiTTC was tested as catalytic precursors for polymerization of styrene in toluene. The maximum polymerization activity was achieved after polymerization period of 20 minutes. Activity decreased in order FSiTTC/MAO > F2SiTTC/MAO > Cl2SiTTC/MAO > ClSiTTC /MAO. Prepared polystyrenes were characterized using 13C NMR spectroscopy and DSC analysis. Syndiotacticity index of obtained PSs was determined by means of Soxhlet extraction with butan-2-one as solvent. Syndiotacticity indexes of PSs obtained by investigated catalysts possessed higher values then those obtained by standard catalysts (CpTiCl3 a Cp*TiCl3) at comparable polymerization conditions.
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Yu, Ning. "Étude de la cinétique de polymérisation radicalaire du styrène dans un réseau tridimensionnel et application à la valorisation de pneus usagés." Thesis, Université de Lorraine, 2015. http://www.theses.fr/2015LORR0277.

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Cette thèse a pour objet de développer une nouvelle méthodologie pour valoriser les poudrettes de pneus usagés (PPU). Celles-ci résultent du broyage de la partie caoutchoutique des pneus usagés qui conserve l’excellente élasticité. L’idée est de profiter de leur élasticité pour renforcer la résistance au choc des polymères fragiles tels que le polystyrène (PS) en y incorporant les PPU. Cependant, la réalisation de cette idée a besoin de relever deux défis majeurs : (1) les PPU commerciales ont typiquement des diamètres de l’ordre de plusieurs centaines de micromètres. Or elles doivent être deux ordres de grandeur plus petits en taille pour pouvoir améliorer la résistance au choc des polymères fragiles. (2) L’adhésion interfaciale entre les polymères et les PPU est mauvaise et constitue donc des défauts mécaniques du matériau. Ces deux défis sont liés à la nature même des PPU qui sont intrinsèquement des réseaux réticulés chimiquement. Cette thèse choisit le PS pour représenter les polymères fragiles. La méthodologie visant à renforcer sa résistance au choc est de polymériser le styrène par voie radicalaire au sein des PPU. Cette polymérisation forme à la fois des chaines en PS libres et des greffons en PS liés chimiquement aux mailles du réseau des PPU. Les inclusions des chaines en PS libres facilitent la dispersion des PPU en taille plus petite lorsqu’une action mécanique leur est appliquée lors de l’extrusion par exemple. La formation des greffons en PS sur les mailles du réseau des PPU renforce l’adhésion interfaciale entre le PS et les PPU. Cette thèse a développé un modèle complet permettant de décrire la cinétique de polymérisation radicalaire du PS libre et celle des greffons en PS liés aux mailles du réseau des PPU. Elle l’a validé par un plan d’expériences judicieux
This thesis aims to develop a novel approach to value ground tire rubber (GTR). The latter results from grounding of the rubber part of used tires which retains excellent elasticity. The idea is to take the advantage of its elasticity to toughen brittle polymers such as polystyrene (PS) upon incorporating GTR into them. However, two challenges have to be overcome to realize this idea. (1) Commercial GTR is typically in the form of particles of a few hundreds of micrometers in diameter. However, it has to be at least one to two orders of magnitude smaller when incorporated in a brittle polymer so as to be able to improve its impact resistance. (2) The interfacial adhesion between the polymer and GTR is weak. These two challenges are related to the intrinsic nature of the GTR which is chemically cross-linked. This thesis chooses PS to represent brittle polymers. The approach aiming at toughening it is to polymerize styrene in a free radical manner inside cross-linked GTR particles. This leads to the formation of both free PS and PS that is grafted onto the GTR, denoted as grafted PS. The inclusions of the free PS inside the GTR particles help break them down by mechanical shear in a screw extruder for example and the formation of grafted PS improves the interfacial adhesion between the PS and the GTR. This thesis has developed a comprehensive kinetic model for the polymerization of free PS and that of grafted PS. This model is validated by experimental designs
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Bao, Jin-Biao. "Elaboration de polypropylène ou de polystyrène à l'aide du dioxyde de carbone supercritique : procédé – microstructure – propriétés mécaniques." Thesis, Vandoeuvre-les-Nancy, INPL, 2011. http://www.theses.fr/2011INPL111N/document.

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Le moussage du polypropylène (PP) et du polystyrène (PS) par le scCO2 est étudié de manière systématique avec l’accent sur la relation entre le procédé, la microstructure et les propriétés mécaniques. La première partie de cette thèse porte sur l’amélioration de la résistance au choc du PP par cristallisation induite par le scCO2. Dans un deuxième temps, le PP fortement orienté avec des structures shish-kebab et sphérolite est utilisé pour étudier l’influence de la structure cristalline sur la nucléation et la croissance des cellules pendant le procédé de moussage sous le scCO2. Ensuite, les influences des conditions de moussage ainsi que celles des paramètres structuraux de la mousse de PS ont été étudiées. Les mousses de PS à cellules isotropes ont été comparées avec celles de PS à cellules orientées. Enfin, un procédé de moussage discontinu en deux étapes est développé afin de produire des mousses de PS à cellules bi-modales en utilisant le scCO2 en tant qu’agent de moussage. Cette structure unique de petites et grandes cellules réparties de manière homogène au travers de l’ensemble du volume de la mousse confère à cette dernière des propriétés particulières
In this work, scCO2 induced foaming of PP or PS is systematically studied with emphasis on the relationship between process, microstructure and mechanical properties. The first part of the thesis deals with the toughening of iPP by scCO2 induced crystallization for the fine separation of rigid crystalline domains and soft amorphous ones in the polymer matrix. The highly oriented iPP with “shish-kebab” and “spherulite” are then used for CO2 foaming to investigate the effect of crystalline structure on the formation of cell nucleation and growth. In addition, the effect of the foaming conditions and the cell structural parameters of PS foams on the mechanical properties are studied systematically. PS foams with isotropic cell morphology and oriented cell one are prepared. Finally, a two-step depressurization batch process is developed to produce bi-modal cell structure PS foams by using scCO2 as the blowing agent. This unique cell structure with both small and large cells homogenously distributed throughout the entire volume of the foam sample might have particular properties
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Zhang, Hui [Verfasser], and Günter [Akademischer Betreuer] Reiter. "Pattern formation on single crystals of isotatic polystyrene in thin films = Strukturbildung von Einkristallen aus isotaktischem Polystyrol in dünnen Filmen." Freiburg : Universität, 2014. http://d-nb.info/1123481717/34.

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Benbayer, Chahinez. "Nanocomposites à base d'argile et de surfactants polymérisables (surfmers) : synthèse et propriétés." Thesis, Nice, 2014. http://www.theses.fr/2014NICE4151/document.

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Le travail présenté dans ce mémoire de thèse porte sur la préparation de nouveaux nanocomposites polystyrène-argile en utilisant des argiles modifiées par divers tensioactifs cationiques polymérisables fluorés. Des systèmes de référence ont aussi été envisagés en utilisant des tensioactifs classiques de structure proche de celles des surfmers (surfmers et tensioactifs hydrocarbonés) et ce, afin de mettre en évidence le rôle joué par le groupement polymérisable et l’atome de fluor sur la structure et les propriétés des nanocomposites obtenus. Les propriétés de surface des tensioactifs ont été étudiées en termes de CMC, tensions de surface et enthalpies de micellisation de Gibbs afin d’évaluer le comportement en solution de ces tensioactifs. Ces tensioactifs ont été par la suite utilisés pour modifier une montmorillonite sodée via un processus d’échange cationique. Les organoargiles ainsi obtenues ont été caractérisées par IR, ATG et DRX. Les données DRX obtenues sont en faveur d’un alignement de la majorité des surfmers fluorés en bicouche La préparation des nanocomposites polystyrène-argile contenant diverses quantités d’organoargiles variant de 1 à 15% en utilisant la technique de polymérisation radicalaire en masse ou en solution, a montré l’effet positif de l’introduction d’une chaîne fluorée et d’une fonction polymérisable sur la stabilité thermique des nanocomposites. Des morphologies exfoliées ont été obtenues pour la majorité des nanocomposites fluorés préparés. Une relation structure-propriétés de surface et propriétés thermique a été établie sur la base des analyses ATG, DRX et TEM/MEB
The work presented in this thesis focuses on the preparation of new polystyrene-clay nanocomposites using fluorinated polymerizable cationic surfactants as modifiers. Reference systems have also been proposed using conventional surfactants of similar structure than surfmers. The main objective is to highlight the role of the polymerizable group and the fluorine atoms on the structure and the properties of the obtained nanocomposites. The surface properties of surfactants were studied in terms of CMC, surface tensions and Gibbs enthalpies of micellization to evaluate the solution behavior of these surfactants. These surfactants were subsequently used to modify a sodium montmorillonite via cation exchange process. The resultant organoclays were characterized by IR, TGA and XRD analysis. XRD data are in favor of an alignment of the majority of fluorinated surfmers to form a bilayer structure while conventional surfactants tend to form a pseudotrimolecular layer. Determination of surfmer reactivity ratios by NMR was used to predict the behavior of these derivatives in radical copolymerization with styrene. Preparation of polystyrene-clay nanocomposite containing various amounts of organoclays from 1 to 15 wt% by radical polymerization process in bulk or solution, showed the positive effect of the introduction of fluorinated chain and polymerizable functional group on thermal stability of nanocomposites. Exfoliated morphologies were obtained for the majority of the fluorinated nanocomposite. A structure-surface and thermal properties relationship was established on the basis of TGA, XRD and TEM / SEM analysis
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Mucklo, Matthew Joseph. "API federation in a polystore." Thesis, Massachusetts Institute of Technology, 2018. https://hdl.handle.net/1721.1/121633.

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This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Thesis: M. Eng., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2018
Cataloged from student-submitted PDF version of thesis.
Includes bibliographical references (pages 97-101).
This thesis describes the design, implementation, test, and evaluation of an extension to a well-known polystore called BigDAWG. As a polystore, BigDAWG binds together multiple diverse data sources into a single system that allows primarily analytical queries to be easily executed against the most appropriate engine for the job. The extension described allows the polystore to source data from APIs such as those publicly available on the internet. Further, an administrative interface was constructed to facilitate the adding, editing, and deleting of access to these APIs. These additions place power into the hands of the BigDAWG polystore user such that not only do they have the ability to source data from many new sources, but can process that data quickly and easily by using the built-in polystore casting facilities, cutting down on the time necessary to create custom ETLs to achieve the same result.
by Matthew Joseph Mucklo.
M. Eng.
M.Eng. Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science
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Books on the topic "Polystyre"

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Ita, Paul A., and Pam Safarek. World polystyrene. Cleveland, Ohio: Freedonia Group, 1998.

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Schellenberg, Jrgen, ed. Syndiotactic Polystyrene. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2009. http://dx.doi.org/10.1002/9780470557006.

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Crevecoeur, J. Water expandable polystyrene (weps). Eindhoven: Eindhoven University ofTechnology, 1997.

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executive, Health and safety. Expanded polystyrene moulding machines. London: H.M.S.O., 1986.

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Books, Roof, ed. Styrofoam. New York: Roof Books, 2009.

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Gray, James E. Polystyrene: Properties, performance, and applications. New York: Nova Science Publishers, 2011.

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Hancox, Robert Neil. Polystyrene pyrolysis: Kinetics and mechanisms. Birmingham: University of Birmingham, 1989.

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Hammond, Timothy. A study of polystyrene pyrolysis. Birmingham: University of Birmingham, 1986.

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Schellenberg, Jürgen. Syndiotactic polystyrene: Synthesis, characterization, processing, and applications. Hoboken, N.J: Wiley, 2010.

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Gadepally, Vijay, Timothy Mattson, Michael Stonebraker, Fusheng Wang, Gang Luo, Yanhui Laing, and Alevtina Dubovitskaya, eds. Heterogeneous Data Management, Polystores, and Analytics for Healthcare. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-33752-0.

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Book chapters on the topic "Polystyre"

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Begoli, Edmon, Sudarshan Srinivasan, and Maria Mahbub. "The Transformers for Polystores - The Next Frontier for Polystore Research." In Heterogeneous Data Management, Polystores, and Analytics for Healthcare, 72–77. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-71055-2_7.

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Bährle-Rapp, Marina. "Polystyrene." In Springer Lexikon Kosmetik und Körperpflege, 441. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_8218.

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Gooch, Jan W. "Polystyrene." In Encyclopedic Dictionary of Polymers, 571–72. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9215.

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Gooch, Jan W. "Polystyrol." In Encyclopedic Dictionary of Polymers, 572. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9221.

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Baker, Ian. "Polystyrene." In Fifty Materials That Make the World, 175–78. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-78766-4_33.

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Peacock, Andrew J., and Allison Calhoun. "Polystyrene." In Polymer Chemistry, 309–23. München: Carl Hanser Verlag GmbH & Co. KG, 2006. http://dx.doi.org/10.3139/9783446433434.021.

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Beyer, Leslie A., and Julie E. Goodman. "Polystyrene/Styrene." In Hamilton & Hardy's Industrial Toxicology, 809–14. Hoboken, New Jersey: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118834015.ch79.

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Gooch, Jan W. "Impact Polystyrene." In Encyclopedic Dictionary of Polymers, 383. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6221.

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Gooch, Jan W. "Expanded Polystyrene." In Encyclopedic Dictionary of Polymers, 285. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_4658.

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Steiner, G., and C. Zimmerer. "Polystyrene (PS)." In Polymer Solids and Polymer Melts – Definitions and Physical Properties I, 997–1005. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32072-9_113.

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Conference papers on the topic "Polystyre"

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Singhal, Rekha, Nathan Zhang, Luigi Nardi, Muhammad Shahbaz, and Kunle Olukotun. "Polystore++: Accelerated Polystore System for Heterogeneous Workloads." In 2019 IEEE 39th International Conference on Distributed Computing Systems (ICDCS). IEEE, 2019. http://dx.doi.org/10.1109/icdcs.2019.00163.

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Jananthan, Hayden, Ziqi Zhou, Vijay Gadepally, Dylan Hutchison, Suna Kim, and Jeremy Kepner. "Polystore mathematics of relational algebra." In 2017 IEEE International Conference on Big Data (Big Data). IEEE, 2017. http://dx.doi.org/10.1109/bigdata.2017.8258298.

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Khan, Yasar, Antoine Zimmermann, AlokKumar Jha, Dietrich Rebholz-Schuhmann, and Ratnesh Sahay. "Querying web polystores." In 2017 IEEE International Conference on Big Data (Big Data). IEEE, 2017. http://dx.doi.org/10.1109/bigdata.2017.8258299.

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Gadepally, Vijay, Peinan Chen, Jennie Duggan, Aaron Elmore, Brandon Haynes, Jeremy Kepner, Samuel Madden, Tim Mattson, and Michael Stonebraker. "The BigDAWG polystore system and architecture." In 2016 IEEE High Performance Extreme Computing Conference (HPEC). IEEE, 2016. http://dx.doi.org/10.1109/hpec.2016.7761636.

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Wang, Jing, David F. James, Chul B. Park, Albert Co, Gary L. Leal, Ralph H. Colby, and A. Jeffrey Giacomin. "Planar Extensional Viscosity of Polystyrene and Polystyrene∕CO[sub 2] Solution." In THE XV INTERNATIONAL CONGRESS ON RHEOLOGY: The Society of Rheology 80th Annual Meeting. AIP, 2008. http://dx.doi.org/10.1063/1.2964859.

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Altavilla, Claudia, Filippo Fedi, Andrea Sorrentino, Salvatore Iannace, and Paolo Ciambelli. "Polystyrene/MoS2@oleylamine nanocomposites." In TIMES OF POLYMERS (TOP) AND COMPOSITES 2014: Proceedings of the 7th International Conference on Times of Polymers (TOP) and Composites. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4876811.

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Podkorytov, Maksim, and Michael Gubanov. "Hybrid.Poly: A Consolidated Interactive Analytical Polystore System." In 2019 IEEE 35th International Conference on Data Engineering (ICDE). IEEE, 2019. http://dx.doi.org/10.1109/icde.2019.00223.

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Zuohao She, Surabhi Ravishankar, and Jennie Duggan. "BigDAWG polystore query optimization through semantic equivalences." In 2016 IEEE High Performance Extreme Computing Conference (HPEC). IEEE, 2016. http://dx.doi.org/10.1109/hpec.2016.7761584.

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Leclercq, Éric, and Marinette Savonnet. "A Tensor Based Data Model for Polystore." In the 22nd International Database Engineering & Applications Symposium. New York, New York, USA: ACM Press, 2018. http://dx.doi.org/10.1145/3216122.3216152.

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Du, Jiang, John Meehan, Nesime Tatbul, and Stan Zdonik. "Towards Dynamic Data Placement for Polystore Ingestion." In BIRTE '17: International Workshop on Real-Time Business Intelligence and Analytics. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3129292.3129297.

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Reports on the topic "Polystyre"

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Abrefah, John, and George S. Klinger. Thermal Decomposition of Radiation-Damaged Polystyrene. Office of Scientific and Technical Information (OSTI), September 2000. http://dx.doi.org/10.2172/965178.

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J Abrefah GS Klinger. Thermal Decomposition of Radiation-Damaged Polystyrene. Office of Scientific and Technical Information (OSTI), September 2000. http://dx.doi.org/10.2172/763386.

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Mulholland, George, Gary Hembree, and Arie Hartman. Sizing of polystyrene spheres produced in microgravity. Gaithersburg, MD: National Bureau of Standards, 1985. http://dx.doi.org/10.6028/nbs.ir.84-2914.

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Guttman, C. M., W. R. Blair, and J. R. Maurey. Recertification of the SRM 706a, a polystyrene. Gaithersburg, MD: National Institute of Standards and Technology, 1998. http://dx.doi.org/10.6028/nist.ir.6091.

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Rao, G. R., L. Riester, and E. H. Lee. Depth-independent hardness improvements in ion irradiated polystyrene. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/34424.

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Cazzaniga, L., and R. E. Cohen. Synthesis and Characterization of Isotactic Polystyrene-Polybutadiene Block Copolymers. Fort Belvoir, VA: Defense Technical Information Center, October 1988. http://dx.doi.org/10.21236/ada201701.

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Largo, Sherly R., Timothy S. Haddad, Rene I. Gonzalez, and Constance Schlaefer. The Specific Refractive Index Increment for Isobutyl Poss-Polystyrene Copolymers. Fort Belvoir, VA: Defense Technical Information Center, January 2003. http://dx.doi.org/10.21236/ada419049.

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Kesavanathan, Jana, and Robert W. Doherty. Test Procedure for Removing Polystyrene Latex Microspheres from Membrane Filters. Fort Belvoir, VA: Defense Technical Information Center, July 1999. http://dx.doi.org/10.21236/ada367979.

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Lettieri, Thomas R., and Gary G. Hembree. Certification of NBS SRM 1691: 0.3�m-diameter polystyrene spheres. Gaithersburg, MD: National Bureau of Standards, January 1988. http://dx.doi.org/10.6028/nbs.ir.87-3730.

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Ding, Zheng-You, Shenmin Ma, Dennis Kriz, J. J. Aklonis, and R. Salovey. Model Filled Polymers .11. Synthesis of Uniformly Crosslinked Polystyrene Microbeads. Fort Belvoir, VA: Defense Technical Information Center, June 1991. http://dx.doi.org/10.21236/ada237472.

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