Academic literature on the topic 'Polyketone'

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Journal articles on the topic "Polyketone"

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Kalinina, I. A., G. P. Belov, K. Z. Gumargalieva, Yu A. Shlyapnikov, and G. E. Zaikov. "Inhibition of polyketone oxidation." Journal of Applied Polymer Science 89, no. 5 (2003): 1182–85. http://dx.doi.org/10.1002/app.12034.

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Lee, Han Ki, Dae Sik Kim, Jong Sung Won, Da Young Jin, Hyun Jae Lee, and Seung Goo Lee. "Effects of Thermal and Humidity Aging on the Interfacial Adhesion of Polyketone Fiber Reinforced Natural Rubber Composites." Advances in Materials Science and Engineering 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/4159072.

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Polyketone fiber is considered as a reinforcement of the mechanical rubber goods (MRG) such as tires, automobile hoses, and belts because of its high strength and modulus. In order to apply it to those purposes, the high adhesion of fiber/rubber interface and good sustainability to aging conditions are very important. In this study, polyketone fiber reinforced natural rubber composites were prepared and they were subjected to thermal and humidity aging, to assess the changes of the interfacial adhesion and material properties. Also, the effect of adhesive primer treatment, based on the resorci
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Du, Jia Yao, Liang Chen, Wen Wei, Lin Deng, Ling Gao, and Jing Wang. "Studies on Influencing Factors of Polyketone Molecular Weight by Palladium Catalyzed Alternating Copolymerization with Carbon Monoxide and Ethylene." Advanced Materials Research 634-638 (January 2013): 2014–18. http://dx.doi.org/10.4028/www.scientific.net/amr.634-638.2014.

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With Pd(AcO)2DPPP as catalytic precursor of CO/C2H4 alternating copolymerization. The main factors which affect the molecular weight of polyketone were studied. The results showed that: Temperature was the most important factor in copolymerization. The polyketone molecular weight lower faster with increasing temperature, have a decrease of 53% when system temperature rise from 70°C to 80°C, and the palladium-catalyzed progenitor easy to decomposition and become deactivation. Adding pressure was in favor of the increase of copolymerization rate and molecular weight. Water content in methanol so
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Marklund, E., U. W. Gedde, M. S. Hedenqvist, and G. Wiberg. "Properties of polyketone/polypropylene blends." Polymer 42, no. 7 (2001): 3153–60. http://dx.doi.org/10.1016/s0032-3861(00)00605-4.

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Lee, Juchul, Kwang Hoon Lee, Daehum Kim, Soonho Lim, and Sang-Soo Lee. "Layered nanofiller-reinforced polyketone composites." Macromolecular Research 21, no. 11 (2013): 1270–73. http://dx.doi.org/10.1007/s13233-013-1173-8.

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Zuiderduin, W. C. J., D. P. N. Vlasveld, J. Huétink, and R. J. Gaymans. "Influence of sample thickness on fracture behaviour of a polyketone and a polyketone-rubber blend." Polymer 46, no. 23 (2005): 10321–30. http://dx.doi.org/10.1016/j.polymer.2005.07.107.

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Kim, Ho-Bae, Seung Yong Lee, and Taek Sung Hwang. "Optimization of Synthesis Process for Aminated Polyketone Anion Exchange Membranes via Response Surface Methodology (RSM)." Polymer Korea 44, no. 4 (2020): 459–70. http://dx.doi.org/10.7317/pk.2020.44.4.459.

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Zuiderduin, W. C. J., J. Huétink, and R. J. Gaymans. "Rigid particle toughening of aliphatic polyketone." Polymer 47, no. 16 (2006): 5880–87. http://dx.doi.org/10.1016/j.polymer.2006.05.077.

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Voortman, Thomas P., Davide Bartesaghi, L. Jan Anton Koster, and Ryan C. Chiechi. "Cross-Conjugated n-Dopable Aromatic Polyketone." Macromolecules 48, no. 19 (2015): 7007–14. http://dx.doi.org/10.1021/acs.macromol.5b01387.

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Bogdanova, Yu G., O. N. Golodkov, S. R. Allayarov, and G. P. Belov. "Adhesive properties of gamma-irradiated polyketone." High Energy Chemistry 51, no. 1 (2017): 6–10. http://dx.doi.org/10.1134/s0018143916060035.

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Dissertations / Theses on the topic "Polyketone"

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Malinova, Violeta. "Synthesis of novel functional poly(1,4-ketone)s bearing pendant bioactive moieties: an approach to design biocompatible materials." [S.l. : s.n.], 2006. http://nbn-resolving.de/urn:nbn:de:bsz:289-vts-56265.

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Lommerts, Bert Jan. "Structure development in polyketone and polyalcohol fibers." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 1994. http://irs.ub.rug.nl/ppn/290728010.

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Sunjuk, Mahmoud Shaker Ahmed. "Emulsion copolymerization of alpha-olefins with carbon monoxide using water-soluble palladium(II) complexes." [S.l. : s.n.], 2003.

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Li, Maohua. "Synthesis of Polyketones from Zwitterionic Nickel Compound Catalyzed Copolymerization of Carbon Monoxide And Olefins." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1461772542.

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He, Shiyu. "Synthesis of New Zwitterionic Nickel(II) Catalyst For Ethylene and Carbon Monoxide Copolymerization." University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1524763348307418.

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Jiang, Bo. "Homo- and co-polymerization of disubstituted ketenes." Thesis, Normandie, 2019. http://www.theses.fr/2019NORMIR02/document.

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Ce travail vise à synthétiser avec un rendement satisfaisant de nouvelles architectures de polymères à hautes performances, possédant une structure définie et une bonne fenêtre de transformation, sur la base de cétènes aliphatiques ou aromatiques disubstitués. Les synthèses de diméthylcétène (DMK), méthyléthylcétène (MEK), diéthylcétène (DEK), éthylphénylcétène (EPK) et diphénylcétène (DPK) ont été étudiées. Puis l’homo- et la copolymérisation de ces monomères avec différents amorceurs ont été étudiées. L’influence de l’encombrement stérique présent sur les cétènes influence grandement leur ré
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Hayki, Najib. "Synthèse et caractérisation de nouveaux polymères obtenus à partir de l'éthylcétène." Phd thesis, INSA de Rouen, 2011. http://tel.archives-ouvertes.fr/tel-00633323.

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L'objectif de cette étude est de synthétiser de nouveaux polymères aux propriétés spécifiques, en utilisant pour la première fois comme monomère un aldocétène : l'éthylcétène. La synthèse de l'éthylcétène a été entreprise en utilisant deux procédés distincts :d'une part la méthode de McCarney, qui a permis de le préparer dans un solvant par entraînement à la vapeur, et d'autre part le craquage de l'anhydride butyrique à 575°C sous 40mbar.La polymérisation ionique de l'éthylcétène a ensuite été réalisée, dans différentes conditions de solvant, de température et avec plusieurs amorceurs. La poly
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Wang, Hanbin. "Synthèse et caractérisation de nouvellespolycétones aliphatiques à partir des cétènes." Phd thesis, INSA de Rouen, 2013. http://tel.archives-ouvertes.fr/tel-00973486.

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L'objectif de cette étude est de synthétiser de nouvelles architectures de polycétones aliphatiques à base de cétènes, possédant une température de fusion plus basse que le polydiméthylcétène, tout en conservant une température de dégradation élevée, afin d'élargir sa fenêtre de mise en œuvre.La synthèse du diméthylcétène et / ou de l'éthylcétène a été réalisée par pyrolyse de l'anhydride isobutyrique et/ou butyrique à 625°C sous 40 mbar. Un copolymère statistique a été d'abord synthétisé par copolymérisation entre le diméthylcétène et l'éthylcétène, par voie cationique à -78°C ; ensuite en ut
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Ndiege, Isaiah Omolo. "Polyketide biosynthesis." Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315331.

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Ignatenko, Vasily A. "MOLECULAR LIBRARY SYNTHESIS USING NATURAL PRODUCTS: EXPANDING THE FRAMEWORK OF STEROIDS AND PENTACYCLIC TRITERPENOIDS." Case Western Reserve University School of Graduate Studies / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=case1384382654.

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Books on the topic "Polyketone"

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O'Hagan, David. The polyketide metabolites. E. Horwood, 1991.

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O'Hagan, David. The polyketide metabolites. Ellis Horwood, 1991.

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Evans, Bradley S., ed. Nonribosomal Peptide and Polyketide Biosynthesis. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3375-4.

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1957-, Rimando Agnes M., Baerson Scott R, and American Chemical Society. Division of Agricultural and Food Chemistry., eds. Polyketides: Biosynthesis, biological activity, and genetic engineering. American Chemical Society, 2007.

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Jenner, Matthew. Using Mass Spectrometry for Biochemical Studies on Enzymatic Domains from Polyketide Synthases. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-32723-5.

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Ahmed Kassem Abd El-Samad El-Sayed. Molecular biological studies on the genes of Pseudomonas fluorescens NC1B10586 which encode biosynthesis of the polyketide antibiotic mupirocin. University of Birmingham, 2001.

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Whatling, Carl Andrew. Molecular analysis of the genes involved in the biosynthesis of pseudomonic acid, a polyketide antibiotic produced by Pseudomonas fluorescens NCIB10586. University of Birmingham, 1993.

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(Editor), Agnes M. Rimando, and Scott R. Baerson (Editor), eds. Polyketides: Biosynthesis, Biological Activity, and Genetic Engineering (Acs Symposium Series). An American Chemical Society Publication, 2006.

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Jenner, Matthew. Using Mass Spectrometry for Biochemical Studies on Enzymatic Domains from Polyketide Synthases. Springer, 2016.

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Fuller, Geoffrey A. Cloning and characterization of a polyketide-like gene cluster from Streptomyces murayamaensis. 1995.

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Book chapters on the topic "Polyketone"

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Gooch, Jan W. "Polyketone Resins." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9115.

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Bashford, David. "Polyketones." In Thermoplastics. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-1531-2_73.

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Martin, Robert, and Jean-Pierre Buisson. "Butanones: Polyketones." In Aromatic Hydroxyketones: Preparation & Physical Properties. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-14185-5_2.

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Nozaki, Kyoko. "Optically Active Polyketones." In Polymeric Chiral Catalyst Design and Chiral Polymer Synthesis. John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118063965.ch14.

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Bashford, David. "Aliphatic Polyketones (APK)." In Thermoplastics. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-1531-2_70.

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Hill, Alison M. "Polyketide Polyethers." In Natural Products in Chemical Biology. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118391815.ch8.

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Katz, Leonard. "Polyketide diversity." In Macrolide Antibiotics. Birkhäuser Basel, 2002. http://dx.doi.org/10.1007/978-3-0348-8105-0_9.

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Buchholz, Tonia J., Jeffrey D. Kittendorf, and David H. Sherman. "Modular Polyketide Synthases." In Natural Products in Chemical Biology. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118391815.ch7.

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Hothersall, Joanne, and Christopher M. Thomas. "Polyketide Antibiotics of Pseudomonas." In Pseudomonas. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9088-4_23.

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Gokhale, Rajesh S., and Dipika Tuteja. "Biochemistry of Polyketide Synthases." In Biotechnology. Wiley-VCH Verlag GmbH, 2008. http://dx.doi.org/10.1002/9783527620937.ch12.

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Conference papers on the topic "Polyketone"

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Matsutani, Hiroshi, Nanako Arima, Youhei Ishikawa, Masahiro Matsunaga, and Yutaka Okada. "Thermally Stable and Transparent Polyketone Resin." In 2019 IEEE CPMT Symposium Japan (ICSJ). IEEE, 2019. http://dx.doi.org/10.1109/icsj47124.2019.8998746.

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Pilz, Gerald, and Peter Guttmann. "Dynamic mechanical profile of polyketone compared to conventional technical plastics." In PROCEEDINGS OF THE REGIONAL CONFERENCE GRAZ 2015 – POLYMER PROCESSING SOCIETY PPS: Conference Papers. Author(s), 2016. http://dx.doi.org/10.1063/1.4965540.

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Waters, Dixie, and Att van Veelen. "Aliphatic Polyketones in Automotive Fuel Systems." In International Congress & Exposition. SAE International, 1995. http://dx.doi.org/10.4271/950364.

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TOWNSEND, CRAIG A. "DECONSTRUCTION OF ITERATIVE POLYKETIDE SYNTHASES." In 23rd International Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2014. http://dx.doi.org/10.1142/9789814603836_0042.

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Nassar, S., B. Liu, and L. Beerhues. "Polyketide-related biosynthesis of plant anthranoids." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399796.

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Bunzel, C., B. Liu, and L. Beerhues. "Novel dual-function type III polyketide synthase from Hypericum polyphyllum." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399659.

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Erokhin, D. V., O. D. Mikityuk, L. A. Shcherbakova, and V. G. Dzhavakhiya. "Inhibition of the biosynthesis of polyketide mycotoxins by microbial metabolites." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.065.

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6-Demethylmevinoliin, a secondary metabolite of Penicillum citrinum, is able to efficiently inhibit the biosynthesis of two polypeptide mycotoxins, aflatoxin B1 and zearalenone, by 92 and 78% of the control, respectively.
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Prediger, Patrícia, and Luiz Carlos Dias. "Synthesis of Polyketide Fragments in Order to Study the Elaiophylin Biosynthesis." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391515128.

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Hiebl, V., D. Wang, EH Heiss, R. Mueller, AG Atanasov, and VM Dirsch. "The polyketide soraphen A exerts beneficial effects on cholesterol homeostasis in macrophages." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3400099.

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Bunnak, W., P. Wonnapinij, A. Sriboonlert, CM Lazarus, and P. Wattana-Amorn. "Assembly of a fungal macrocyclic polylactone is catalyzed by two iterative polyketide synthases." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399787.

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Reports on the topic "Polyketone"

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Barron, Andrew R. Tert-butylalumoxanes: Synthetic Analogs for Methylalumoxane (MAO) and New Catalytic Routes to Polyolefins and Polyketones. Defense Technical Information Center, 1994. http://dx.doi.org/10.21236/ada280511.

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Marimo, Patience. Steps Towards Deciphering the Post-Polyketide Synthase Tailoring Steps in the Phoslactomycin Biosynthesis Pathway. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2405.

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