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Journal articles on the topic 'Polyketone'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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1

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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2

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 resorcinol formaldehyde resin and latex (RFL), of polyketone fiber for high interfacial adhesion was evaluated. Morphological and property changes of the rubber composites were analyzed by using various instrumental analyses. As a result, the rubber composite was aged largely by thermal aging at high temperature rather than humidity aging condition. Interfacial adhesion of the polyketone/NR composites was improved by the primer treatment and its effect was maintained in aging conditions.

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3

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 solvent was sensitive to copolymerization rate, as far as molecular weight was concerned, it made no difference. HClO4 and other strong acids in the catalytic system will help improve the molecular weight of the polyketone.

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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Mensitieri, G., M. A. Del Nobile, A. Sommazzi, and L. Nicolais. "Water transport in a polyketone terpolymer." Journal of Polymer Science Part B: Polymer Physics 33, no. 9 (1995): 1365–70. http://dx.doi.org/10.1002/polb.1995.090330906.

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12

Zuiderduin, W. C. J., J. Huétink, and R. J. Gaymans. "Notch sensitivity of aliphatic polyketone terpolymers." Journal of Applied Polymer Science 91, no. 4 (2003): 2558–75. http://dx.doi.org/10.1002/app.13420.

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13

Nam, Jeong Ung, Eun Yeob Choi, Hye Jin Park, and C. K. Kim. "Fabrication of polyketone-grafted multi-walled carbon nanotubes using Grignard reagent and their composites with polyketone." Composites Science and Technology 167 (October 2018): 199–205. http://dx.doi.org/10.1016/j.compscitech.2018.07.043.

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14

Zhang, Lei, Liang Cheng, Haochen Wu, Tomohisa Yoshioka, and Hideto Matsuyama. "One-step fabrication of robust and anti-oil-fouling aliphatic polyketone composite membranes for sustainable and efficient filtration of oil-in-water emulsions." Journal of Materials Chemistry A 6, no. 47 (2018): 24641–50. http://dx.doi.org/10.1039/c8ta10071c.

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15

Zhou, Yi-Cun, Zheng-Min Zhang, Ling Zhou, et al. "Imidazole-functionalized polyketone-based polyelectrolytes with efficient ionic channels and superwettability for alkaline polyelectrolyte fuel cells and multiple liquid purification." Journal of Materials Chemistry A 9, no. 26 (2021): 14827–40. http://dx.doi.org/10.1039/d1ta03460j.

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16

Hou, Jian, Chanju Park, Wongi Jang, and Hongsik Byun. "Facile fabrication and characterization of aliphatic polyketone (PK) micro/nano fiber membranes via electrospinning and a post treatment process." RSC Advances 11, no. 2 (2021): 678–83. http://dx.doi.org/10.1039/d0ra08119a.

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17

Zuiderduin, W. C. J., D. P. N. Vlasveld, J. Huétink, and R. J. Gaymans. "Mechanical properties of polyketone terpolymer/rubber blends." Polymer 45, no. 11 (2004): 3765–79. http://dx.doi.org/10.1016/j.polymer.2004.03.080.

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18

Backman, A., J. Lange, and M. S. Hedenqvist. "Transport properties of uniaxially oriented aliphatic polyketone." Journal of Polymer Science Part B: Polymer Physics 42, no. 6 (2004): 947–55. http://dx.doi.org/10.1002/polb.10688.

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19

Ibidapo, T. Adesanya. "Polyketone and complex formation of some halatopolymers." Polymer Engineering and Science 29, no. 12 (1989): 777–81. http://dx.doi.org/10.1002/pen.760291205.

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20

Bulakh, Neelima, S. M. Kulkarni, J. P. Jog, and R. V. Chaudhari. "Preparation and Characterization of Polyketone/Clay Nanocomposites." Journal of Macromolecular Science, Part B 42, no. 5 (2003): 963–73. http://dx.doi.org/10.1081/mb-120023551.

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21

Chiechi, R. C., G. Sonmez, and F. Wudl. "A Robust Electroactive n-Dopable Aromatic Polyketone." Advanced Functional Materials 15, no. 3 (2005): 427–32. http://dx.doi.org/10.1002/adfm.200400291.

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22

Yang, Yan, Si-Yuan Li, Rui-Ying Bao, et al. "Progress in polyketone materials: blends and composites." Polymer International 67, no. 11 (2018): 1478–87. http://dx.doi.org/10.1002/pi.5624.

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23

Vodyakov, Vladimir N., Alexandr V. Kotin, Vyacheslav V. Kuznetsov, Kseniya A. Kulikovskaya, Elena A. Radaykina, and Mariya I. Murneva. "The Effect of Thermal Degradation Processes on the Physical-Mechanical and Rheological Properties of Polyketone." Key Engineering Materials 869 (October 2020): 140–45. http://dx.doi.org/10.4028/www.scientific.net/kem.869.140.

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The effect of polyketone thermal processing duration on the rheological properties of the melts and the physical and mechanical characteristics of the samples, obtained by injection and compression molding methods, is studied.

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24

Hiroyuki Hata, Sakayu Shimizu, Shizuo Hattori, and Hideaki Yamada. "Ketopantoyl lactone reductase is a conjugated polyketone reductase." FEMS Microbiology Letters 58, no. 1 (1989): 87–90. http://dx.doi.org/10.1111/j.1574-6968.1989.tb03023.x.

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25

Nozaki, Kyoko, Naoyuki Kosaka, Shin-ichi Muguruma та Tamejiro Hiyama. "Asymmetric Reduction of an Enantiomerically Pure γ-Polyketone". Macromolecules 33, № 15 (2000): 5340–46. http://dx.doi.org/10.1021/ma000424d.

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26

Lu, Xuehong, Kim Yong Lim, Fang Yin Lim, Lihua Liu, Shing-Chung Wong, and Jianhong Zhao. "Morphology and structures of polypropylene-aliphatic polyketone blends." Plastics, Rubber and Composites 31, no. 4 (2002): 147–50. http://dx.doi.org/10.1179/146580102225001382.

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27

Guo, JinTang, YaQin Ye, Shan Gao, and YaKai Feng. "Synthesis of polyketone catalyzed by Pd/C catalyst." Journal of Molecular Catalysis A: Chemical 307, no. 1-2 (2009): 121–27. http://dx.doi.org/10.1016/j.molcata.2009.03.017.

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28

Hayki, Najib, Nicolas Desilles, and Fabrice Burel. "Aliphatic polyketone obtained by cationic polymerization of ethylketene." Polymer Chemistry 2, no. 10 (2011): 2350. http://dx.doi.org/10.1039/c1py00199j.

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29

Wakker, A. "Lower critical demixing of a polyketone in hexafluoroisopropanol." Polymer 32, no. 2 (1991): 279–83. http://dx.doi.org/10.1016/0032-3861(91)90014-a.

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30

Zuigyo, Yugo, and Masahiko Yamamoto. "Basic Study of PK Fiber Tire Cord3." Tire Science and Technology 35, no. 4 (2007): 317–25. http://dx.doi.org/10.2346/1.2802609.

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Abstract Rayon, nylon, and polyester have been used for a long time as general tire reinforcements. Recently application of p-aramid fiber, which has high tenacity and high modulus properties, is gradually increasing in order to satisfy high-performance requirements, large tires, and tire weight reduction. However, in working with high-strength and high-modulus fibers such as p-aramid it is normally difficult to obtain excellent adhesion with simple processing methods and their fatigue resistances are not good. This time we have focused on a new high-tenacity and high-modulus “polyketone” fiber obtained by gel-spun technology and performed a basic study in tire cord application. Through laboratory evaluation, we have confirmed that polyketone cord fiber has excellent adhesion, comparable with rayon and nylon, and good fatigue resistance in comparison with rayon. In addition, through its tire evaluation as a body-ply cord and cap-ply cord for PCR tires, we have confirmed its performance advantage in comparison to current tire cords.

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31

Araya-Hermosilla, Esteban Alejandro, Marco Carlotti, Francesco Picchioni, Virgilio Mattoli, and Andrea Pucci. "Electrically-Conductive Polyketone Nanocomposites Based on Reduced Graphene Oxide." Polymers 12, no. 4 (2020): 923. http://dx.doi.org/10.3390/polym12040923.

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In this work, we investigated the functionalization of polyketone 30 (PK30) with glycyl-glycine (Gly-Gly) via the Paal–Knorr reaction with the aim of homogenously dispersing two types of reduced graphene oxide (rGO, i.e., lrGO and hrGO, the former characterized by a lower degree of reduction in comparison to the latter) by non-covalent interactions. The functional PK30-Gly-Gly polymer was effective in preparing composites with homogeneously distributed rGO characterized by an effective percolation threshold at 5 wt. %. All the composites showed a typical semiconductive behavior and stable electrical response after several heating/cooling cycles from 30 to 115 °C. Composites made by hrGO displayed the same resistive behaviour even if flanked by a considerable improvement on conductivity, in agreement with the more reduced rGO content. Interestingly, no permanent percolative network was shown by the composite with 4 wt. % of lrGO at temperatures higher than 45 °C. This material can be used as an ON–OFF temperature sensor and could find interesting applications as sensing material in soft robotics applications.

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32

Kosaka, Naoyuki, Tamejiro Hiyama, and Kyoko Nozaki. "Baeyer−Villiger Oxidation of an Optically Active 1,4-Polyketone." Macromolecules 37, no. 12 (2004): 4484–87. http://dx.doi.org/10.1021/ma0359638.

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33

Ol'khov, Yu A., Yu N. Smirnov, O. A. Golodkov, and G. P. Belov. "Molecular Topology Structure of a Polyketone Modified with Amines." International Polymer Science and Technology 32, no. 1 (2005): 46–56. http://dx.doi.org/10.1177/0307174x0503200108.

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34

Qin, Hui-Min, Akihiro Yamamura, Takuya Miyakawa, et al. "Structure change for substrate recognition in conjugated polyketone reductase." Acta Crystallographica Section A Foundations of Crystallography 69, a1 (2013): s303. http://dx.doi.org/10.1107/s0108767313097377.

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35

Brookhart, M., and Mark I. Wagner. "Synthesis of a Stereoblock Polyketone through Ancillary Ligand Exchange." Journal of the American Chemical Society 118, no. 30 (1996): 7219–20. http://dx.doi.org/10.1021/ja9610141.

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36

Iasilli, Giuseppe, Marco Scatto, and Andrea Pucci. "Vapochromic polyketone films based on aggregation‐induced enhanced emission." Polymers for Advanced Technologies 30, no. 5 (2018): 1160–64. http://dx.doi.org/10.1002/pat.4317.

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37

Koide, Yoshihiro, and Andrew R. Barron. "Polyketone Polymers Prepared Using a Palladium/Alumoxane Catalyst System." Macromolecules 29, no. 4 (1996): 1110–18. http://dx.doi.org/10.1021/ma951369p.

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38

Frapper, Gilles, Chang-Xing Cu, Miklos Kertesz, et al. "Can carbon monoxide polymerize? A theoretical investigation of polyketone." Chemical Communications, no. 20 (1997): 2011. http://dx.doi.org/10.1039/a705721k.

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39

Hamarneh, A. I., H. J. Heeres, A. A. Broekhuis, K. A. Sjollema, Y. Zhang, and F. Picchioni. "Use of soy proteins in polyketone-based wood adhesives." International Journal of Adhesion and Adhesives 30, no. 7 (2010): 626–35. http://dx.doi.org/10.1016/j.ijadhadh.2010.06.002.

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40

Agostinelli, E., F. Belli, G. Tempera, et al. "Polyketone polymer: A new support for direct enzyme immobilization." Journal of Biotechnology 127, no. 4 (2007): 670–78. http://dx.doi.org/10.1016/j.jbiotec.2006.08.011.

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41

Del Nobile, M. A., G. Mensitieri, and A. Sommazzi. "Gas and water vapour transport in a polyketone terpolymer." Polymer 36, no. 26 (1995): 4943–50. http://dx.doi.org/10.1016/0032-3861(96)81619-3.

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42

You, Jiwan, Han-Hyeong Choi, Tae Ann Kim, et al. "High-performance polyketone nanocomposites achieved via plasma-assisted mechanochemistry." Composites Science and Technology 183 (October 2019): 107800. http://dx.doi.org/10.1016/j.compscitech.2019.107800.

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43

Nozaki, K. "Asymmetric catalytic synthesis of polyketones and polycarbonates." Pure and Applied Chemistry 76, no. 3 (2004): 541–46. http://dx.doi.org/10.1351/pac200476030541.

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Two examples are presented for the synthesis of optically active polymers with main-chain chirality from achiral monomers using chiral metal-complexes as catalysts. Asymmetric alternating copolymerization of α-olefins with carbon monoxide provided optically active polyketones when catalyzed by an (R,S)-BINAPHOS-Pd complex. From propene and CO, highly isotactic polyketone with high enantioselectivity (>97 % like diad and >95 % ee). Spectroscopic and theoretical studies revealed that the olefin insertion is the key step for the enantiofacial selection and that this step takes place at cis to the phosphine part of (R,S)-BINAPHOS. The catalyst is applicable not only to propene/CO but also to styrene/CO, which enabled the first asymmetric terpolymerization of propene/styrene/CO. The catalyst tolerates funational groups such as fluorocarbons and a nitrile group so that they can be incorporated in the side chain. Optically active polycarbonate was also synthesized by the alternating copolymerization of cyclohexene oxide with carbon dioxide via the desymmetrization of the meso-epoxide. Dinuclei zinc species prepared from diethylzinc, ethanol, and α,α'-diphenylprolinol, was revealed to be the real active species.

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44

Yang, Jinlian, та Harry W. Gibson. "Polyketone Synthesis Involving Nucleophilic Substitution via Carbanions Derived from Bis(α-amino nitrile)s. 2.1Wholly Aromatic Polyketones without Ether Linkages". Macromolecules 30, № 19 (1997): 5629–33. http://dx.doi.org/10.1021/ma961417l.

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45

A. Paquette, Leo, and Ryan E. Hartung. "Homologation of Vicinal Polyketone Networks to Epoxy Ketones with Diazomethane." HETEROCYCLES 64, no. 1 (2004): 23. http://dx.doi.org/10.3987/com-04-s(p)9.

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46

Araya-Hermosilla, Rodrigo, Andrea Pucci, Patrizio Raffa, et al. "Electrically-Responsive Reversible Polyketone/MWCNT Network through Diels-Alder Chemistry." Polymers 10, no. 10 (2018): 1076. http://dx.doi.org/10.3390/polym10101076.

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This study examines the preparation of electrically conductive polymer networks based on furan-functionalised polyketone (PK-Fu) doped with multi-walled carbon nanotubes (MWCNTs) and reversibly crosslinked with bis-maleimide (B-Ma) via Diels-Alder (DA) cycloaddition. Notably, the incorporation of 5 wt.% of MWCNTs results in an increased modulus of the material, and makes it thermally and electrically conductive. Analysis by X-ray photoelectron spectroscopy indicates that MWCNTs, due to their diene/dienophile character, covalently interact with the matrix via DA reaction, leading to effective interfacial adhesion between the components. Raman spectroscopy points to a more effective graphitic ordering of MWCNTs after reaction with PK-Fu and B-Ma. After crosslinking the obtained composite via the DA reaction, the softening point (tan(δ) in dynamic mechanical analysis measurements) increases up to 155 °C, as compared to the value of 130 °C for the PK-Fu crosslinked with B-Ma and that of 140 °C for the PK-Fu/B-Ma/MWCNT nanocomposite before resistive heating (responsible for crosslinking). After grinding the composite, compression moulding (150 °C/40 bar) activates the retro-DA process that disrupts the network, allowing it to be reshaped as a thermoplastic. A subsequent process of annealing via resistive heating demonstrates the possibility of reconnecting the decoupled DA linkages, thus providing the PK networks with the same thermal, mechanical, and electrical properties as the crosslinked pristine systems.

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47

Kim, Yongho, Choon Soo Lee, Sunghun Kim, Hogun Jung, and Jae Young Jho. "Reactive compatibilization of polyketone/ethylene-octene rubber blends by diaminodecane." Macromolecular Research 23, no. 10 (2015): 965–70. http://dx.doi.org/10.1007/s13233-015-3119-9.

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48

Golodkov, O. N., Yu A. Ol’khov, S. R. Allayarov та ін. "The effect of γ-irradiation on laser ablation of polyketone". High Energy Chemistry 47, № 3 (2013): 77–82. http://dx.doi.org/10.1134/s001814391303003x.

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49

Ohsawa, Osamu, Keun-Hyung Lee, Byoung-Suhk Kim, Sumin Lee, and Ick-Soo Kim. "Preparation and characterization of polyketone (PK) fibrous membrane via electrospinning." Polymer 51, no. 9 (2010): 2007–12. http://dx.doi.org/10.1016/j.polymer.2010.02.045.

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50

Held, Anke, Ludmila Kolb, Martin A. Zuideveld, et al. "Aqueous Polyketone Latices Prepared with Water-Insoluble Palladium(II) Catalysts." Macromolecules 35, no. 9 (2002): 3342–47. http://dx.doi.org/10.1021/ma0120411.

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