Добірка наукової літератури з теми "Phosphonate polymers"
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Статті в журналах з теми "Phosphonate polymers"
Amjad, Zahid, and Amannie Kweik. "HYDROXYAPATITE DISPERSION BY PHOSPHONATES, POLYMERS AND PHOSPHONATE/POLYMER BLENDS." Phosphorus Research Bulletin 30 (2015): 19–25. http://dx.doi.org/10.3363/prb.30.19.
Повний текст джерелаDolan, Ciarán, Briar Naysmith, Simon F. R. Hinkley, Ian M. Sims, Margaret A. Brimble, David E. Williams, and Jianyong Jin. "Synthesis of Novel Triazole-Containing Phosphonate Polymers." Australian Journal of Chemistry 68, no. 4 (2015): 680. http://dx.doi.org/10.1071/ch14513.
Повний текст джерелаSqueo, Benedetta Maria, Francesco Carulli, Elisa Lassi, Francesco Galeotti, Umberto Giovanella, Silvia Luzzati, and Mariacecilia Pasini. "Benzothiadiazole-based conjugated polyelectrolytes for interfacial engineering in optoelectronic devices." Pure and Applied Chemistry 91, no. 3 (March 26, 2019): 477–88. http://dx.doi.org/10.1515/pac-2018-0925.
Повний текст джерелаMeng, Bin, Yingying Fu, Zhiyuan Xie, Jun Liu, and Lixiang Wang. "Phosphonated conjugated polymers for polymer solar cells with a non-halogenated solvent process." Polymer Chemistry 6, no. 5 (2015): 805–12. http://dx.doi.org/10.1039/c4py01294a.
Повний текст джерелаJordan, Myles M., and Michael Johnston. "Enhanced Carbonate Scale Inhibition in the North Sea via Synergistic Inhibitor Molecule Blends." Journal of Petroleum Technology 75, no. 01 (January 1, 2023): 44–49. http://dx.doi.org/10.2118/0123-0044-jpt.
Повний текст джерелаVenkatramaiah, Nutalapati, Ricardo F. Mendes, Artur M. S. Silva, João P. C. Tomé, and Filipe A. Almeida Paz. "A ladder coordination polymer based on Ca2+and (4,5-dicyano-1,2-phenylene)bis(phosphonic acid): crystal structure and solution-state NMR study." Acta Crystallographica Section C Structural Chemistry 72, no. 9 (August 25, 2016): 685–91. http://dx.doi.org/10.1107/s2053229616012328.
Повний текст джерелаGelfand, Benjamin S., Jared M. Taylor, and George K. H. Shimizu. "Extracting structural trends from systematic variation of phosphonate/phosphonate monoester coordination polymers." CrystEngComm 19, no. 27 (2017): 3727–36. http://dx.doi.org/10.1039/c7ce00579b.
Повний текст джерелаPapathanasiou, Konstantinos E., Maria Vassaki, Argyro Spinthaki, Fanouria-Eirini G. Alatzoglou, Eleftherios Tripodianos, Petri Turhanen, and Konstantinos D. Demadis. "Phosphorus chemistry: from small molecules, to polymers, to pharmaceutical and industrial applications." Pure and Applied Chemistry 91, no. 3 (March 26, 2019): 421–41. http://dx.doi.org/10.1515/pac-2018-1012.
Повний текст джерелаParvulescu, Viorica, Adriana Popa, Gabriela Paun, Ramona Ene, Corneliu-Mircea Davidescu, and Gheorghe Ilia. "Effect of polymer support functionalization on enzyme immobilization and catalytic activity." Pure and Applied Chemistry 86, no. 11 (November 1, 2014): 1793–803. http://dx.doi.org/10.1515/pac-2014-0715.
Повний текст джерелаBrianna Barbu. "Phosphonate polymers for greener MRI color." C&EN Global Enterprise 101, no. 27 (August 21, 2023): 7. http://dx.doi.org/10.1021/cen-10127-scicon5.
Повний текст джерелаДисертації з теми "Phosphonate polymers"
Cave, Dale. "Synthesis of phosphonate chains, rings and polymers." Thesis, University of Cambridge, 2004. https://www.repository.cam.ac.uk/handle/1810/251903.
Повний текст джерелаWolf, Thomas [Verfasser]. "Poly(phosphonate)s: versatile polymers for biomedical applications / Thomas Wolf." Mainz : Universitätsbibliothek Mainz, 2018. http://d-nb.info/1154464571/34.
Повний текст джерелаZoulalian, Vincent. "Functionalization of titanium oxide surfaces by means of poly(alkyl-phosphonate) polymers." Zürich : ETH, 2008. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=17618.
Повний текст джерелаSingla, Nisha. "Synthesis and characterization of diorganotin(IV) coordination polymers derived from silaalkylphosphonate and sulfonate based ligands." Thesis, IIT Delhi, 2016. http://localhost:8080/iit/handle/2074/7092.
Повний текст джерелаHeering, Christian [Verfasser], Christoph [Akademischer Betreuer] [Gutachter] Janiak, and Christian [Gutachter] Ganter. "New metal-organic frameworks and coordination polymers constructed from bifunctional linkers with carboxylate, pyrazolate and phosphonate / Christian Heering. Betreuer: Christoph Janiak. Gutachter: Christoph Janiak ; Christian Ganter." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2016. http://d-nb.info/1107540216/34.
Повний текст джерелаYoule, Peter. "Phosphonated polymers for nanofibrous tissue scaffolds." Thesis, University of Manchester, 2017. https://www.research.manchester.ac.uk/portal/en/theses/phosphonated-polymers-for-nanofibrous-tissue-scaffolds(74ec59c4-a062-4b98-b86a-7cefe5b59f4b).html.
Повний текст джерелаNegrell-Guirao, Claire. "Synthèse de monomères, télomères et (co)polymères allyliques phosphonés et leurs applications en ignifugation." Thesis, Montpellier 2, 2010. http://www.theses.fr/2010MON20021/document.
Повний текст джерелаSince July 2008, a wide rnage of halogenated flame retardants was withdrawed from the market for environmental problems by the European Union. The phosphorous products turn out to be promising candidates. Within the framework of my thesis, the synthesis of allyl cyclic phosphonated monomers is described as well as their telomerization, polymerization and copolymerization in solution using a radical process). Their flame retardant behavior was also evaluated. Allyl cyclic phosphonated monomers are synthesized by transesterification between a glycol with a double bond and hydrogenophosphonate. An NMR study of the obtained diastereoisomers allowed us to fully understand the structure of these compounds. Radical homopolymerization of hydrogenated dioxaphosphorinane, in the presence of AIBN as initiator, allowed us to obtain polymers with two molar mass distributions: one for oligomers and one for polymers of higher molar mass. This second species is due to a hyperbranched structure showing poor solubility in common solvents, which damage the future applications. The telomerization of the same monomer was carried out using dimethyl hydrogenophosphonate as chain transfer agent leading only one population of oligomers. Furtehrmore, the replacement of the hydrogen linked to phosphorus by an alkyl or aryl group simplify the mechanism of polymerization since only linear oligomers are obtained. Acceptor-donor copolymerization of maleic anhydride and phosphonated allyl ethers, allowed producing alternated copolymers with the opportunity to introduce different reactive groups such as carboxylic acids. Then, oligomers were produced by radical polymerization of phosphonated allyl amine in order to potentially use the nitrogen-phosphorus synergy. An overview of all the phosphonated polymers previously synthesized, was done with the aim of testing their flame retardant performances. Thermogravimetric analysis showed a good thermal behavior of the telomers and the copolymers, similar heat release rate was observed by microcalorimeter compare to commercial product. High efficiency of these phosphorus-containing flame retardants polymers was finally evidenced by using the cone calorimeter on textile
Ju, Lin. "Non-Covalent Interactions in Polymeric Materials: From Ionomers to Polymer Blends." Diss., Virginia Tech, 2019. http://hdl.handle.net/10919/102651.
Повний текст джерелаDoctor of Philosophy
Lu, Ling. "Synthesis and properties of pillared and non-pillared metal organo-phosphates and phosphonates." Thesis, University of Liverpool, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385318.
Повний текст джерелаMyrex, Ronald Dustan. "Synthesis and characterization of phosphorus-containing inorganic polymers." Birmingham, Ala. : University of Alabama at Birmingham, 2007. https://www.mhsl.uab.edu/dt/2007r/myrex.pdf.
Повний текст джерелаAdditional advisors: Houston Boyd, Tracy Hamilton, Christopher Lawson, Charles Watkins. Description based on contents viewed Feb. 8, 2008; title from title screen. Includes bibliographical references.
Книги з теми "Phosphonate polymers"
Troev, Kolio D. Polyphosphoesters: Chemistry and Application. Elsevier, 2012.
Знайти повний текст джерелаTroev, Kolio D. Polyphosphoesters: Chemistry and Application. Elsevier Science & Technology Books, 2012.
Знайти повний текст джерелаЧастини книг з теми "Phosphonate polymers"
Gooch, Jan W. "Dibutyl Butyl Phosphonate." In Encyclopedic Dictionary of Polymers, 207. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3526.
Повний текст джерелаGooch, Jan W. "Di(2-ethylhexyl) 2-Ethylhexyl Phosphonate." In Encyclopedic Dictionary of Polymers, 217. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3632.
Повний текст джерелаPapathanasiou, Konstantinos E., and Konstantinos D. Demadis. "Polymeric Matrices for the Controlled Release of Phosphonate Active Agents for Medicinal Applications." In Handbook of Polymers for Pharmaceutical Technologies, 89–124. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119041559.ch4.
Повний текст джерелаSakaguchi, Yoshimitsu, Kota Kitamura, Junko Nakao, Shiro Hamamoto, Hiroshi Tachimori, and Satoshi Takase. "Preparation and Properties of Sulfonated or Phosphonated Polybenzimidazoles and Polybenzoxazoles." In Functional Condensation Polymers, 95–104. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/0-306-47563-4_8.
Повний текст джерелаPapathanasiou, Konstantinos E., Maria Vassaki, Argyro Spinthaki, Argyri Moschona, and Konstantinos D. Demadis. "Silica-Based Polymeric Gels as Platforms for Delivery of Phosphonate Pharmaceutics." In Polymer Gels, 127–40. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6083-0_5.
Повний текст джерелаSouthard, G. E., K. A. Van Houten, Edward W. Ott, and G. M. Murray. "Synthesis and Spectroscopic Characterization of Molecularly Imprinted Polymer Phosphonate Sensors." In ACS Symposium Series, 19–37. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0980.ch002.
Повний текст джерелаSchwetlick, Klaus. "Mechanisms of Antioxidant Action of Phosphite and Phosphonite Esters." In Mechanisms of Polymer Degradation and Stabilisation, 23–60. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-3838-3_2.
Повний текст джерелаWolf, Thomas, and Frederik R. Wurm. "Chapter 10. Organocatalytic Ring-opening Polymerization Towards Poly(cyclopropane)s, Poly(lactame)s, Poly(aziridine)s, Poly(siloxane)s, Poly(carbosiloxane)s, Poly(phosphate)s, Poly(phosphonate)s, Poly(thiolactone)s, Poly(thionolactone)s and Poly(thiirane)s." In Polymer Chemistry Series, 406–72. Cambridge: Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/9781788015738-00406.
Повний текст джерела"Dibutyl butyl phosphonate." In Encyclopedic Dictionary of Polymers, 277. New York, NY: Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-30160-0_3473.
Повний текст джерела"Di(2-ethylhexyl) 2-ethylhexyl phosphonate." In Encyclopedic Dictionary of Polymers, 290. New York, NY: Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-30160-0_3579.
Повний текст джерелаТези доповідей конференцій з теми "Phosphonate polymers"
Shaw, S. S. S., and K. S. S. Sorbie. "Synergistic Properties of Phosphonate and Polymeric Scale Inhibitor Blends for Barium Sulphate Scale Inhibition." In SPE International Oilfield Scale Conference and Exhibition. SPE, 2014. http://dx.doi.org/10.2118/spe-169752-ms.
Повний текст джерелаJordan, Myles, Kim Vikshåland, and Michael Johnston. "Synergistic Scale Inhibitor Blends Provide Enhanced Carbonate Scale Management- Laboratory to Field." In SPE International Conference on Oilfield Chemistry. SPE, 2023. http://dx.doi.org/10.2118/213843-ms.
Повний текст джерелаSilva, Célia, Alan Beteta, Katherine McIver, and Ken Sorbie. "The Impact of EOR Polymers on the Adsorption of Phosphonate Scale Inhibitors." In SPE International Conference on Oilfield Chemistry. SPE, 2023. http://dx.doi.org/10.2118/213820-ms.
Повний текст джерелаZhang, Y., J. K. K. Daniels, J. Hardy-Fidoe, C. Durnell, M. E. Broussard, E. Hammond, and X. Huang. "Scale Inhibitor Residual Analysis: Twenty-first Century Approach." In SPE International Oilfield Scale Conference and Exhibition. SPE, 2014. http://dx.doi.org/10.2118/spe-169773-ms.
Повний текст джерелаYao, Xuanzhu, Xin Wang, Saebom Ko, Cianna Leschied, Yu Yi Shen, Daniel Pimentel, Chanaka Navarathna, et al. "Fate and Transport of Sulfonated Polymeric Inhibitors in the Reservoir: Studied by Column Experiments With Calcite Media." In SPE International Conference on Oilfield Chemistry. SPE, 2023. http://dx.doi.org/10.2118/213787-ms.
Повний текст джерелаYan, Fei, Amy T. Kan, Chao Yan, Lu Wang, Ya Liu, and Mason B. Tomson. "Experimental and Modeling Study on Enhancement of Squeeze Treatment in Sandstone by the Addition of Zinc Ion." In SPE International Oilfield Scale Conference and Exhibition. SPE, 2014. http://dx.doi.org/10.2118/spe-169753-ms.
Повний текст джерелаXu, Bo, Tao Chen, Ping Chen, Harry Montgomerie, Thomas Hagen, Qi Guo, and Xu Yang. "Influence of Calcium and Bicarbonate Ions on the Kinetics of CaCO3 Formation at High Temperature in the Absence and Presence of Scale Inhibitors." In SPE International Oilfield Scale Conference and Exhibition. SPE, 2014. http://dx.doi.org/10.2118/spe-169769-ms.
Повний текст джерелаLiu, Ya, Rebecca Vilain, and Dong Shen. "How Does EOR Polymer Impact Scale Control During ASP Flooding?" In SPE International Conference on Oilfield Chemistry. SPE, 2021. http://dx.doi.org/10.2118/204350-ms.
Повний текст джерелаJohnston, Clare, and Louise Sutherland. "The Influence of Turbulence (or Hydrodynamic Effects) on Strontium Sulphate Scale Formation and Inhibitor Performance." In SPE International Oilfield Scale Conference and Exhibition. SPE, 2014. http://dx.doi.org/10.2118/spe-169760-ms.
Повний текст джерелаShaw, S. S., and K. S. Sorbie. "Synergistic Properties of Phosphonate and Polymeric Scale Inhibitor Blends for Barium Sulphate Scale Inhibition." In SPE International Oilfield Scale Conference and Exhibition. Society of Petroleum Engineers, 2014. http://dx.doi.org/10.2118/169752-ms.
Повний текст джерела