Academic literature on the topic 'Hyper-Crosslinked polymers'

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Journal articles on the topic "Hyper-Crosslinked polymers"

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Rubin Pedrazzo, Alberto, Fabrizio Caldera, Marco Zanetti, Silvia Lucia Appleton, Nilesh Kumar Dahkar, and Francesco Trotta. "Mechanochemical green synthesis of hyper-crosslinked cyclodextrin polymers." Beilstein Journal of Organic Chemistry 16 (June 29, 2020): 1554–63. http://dx.doi.org/10.3762/bjoc.16.127.

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Cyclodextrin nanosponges (CD-NS) are nanostructured crosslinked polymers made up of cyclodextrins. The reactive hydroxy groups of CDs allow them to act as multifunctional monomers capable of crosslinking to bi- or multifunctional chemicals. The most common NS synthetic pathway consists in dissolving the chosen CD and an appropriate crosslinker in organic polar aprotic liquids (e.g., N,N-dimethylformamide or dimethyl sulfoxide), which affect the final result, especially for potential biomedical applications. This article describes a new, green synthetic pathway through mechanochemistry, in part
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Guo, Ziyang, Xiaodong Tian, Yan Song, et al. "Hard Carbons Derived from Phenyl Hyper-Crosslinked Polymers for Lithium-Ion Batteries." Coatings 13, no. 2 (2023): 421. http://dx.doi.org/10.3390/coatings13020421.

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Hyper-crosslinked polymers are attracting extensive attention owing to their ease of design and synthesis. Based on the flexibility of its molecular design, a hyper-crosslinked polymer with a π-conjugated structure and its derived carbon were synthesized by the Friedel–Crafts reaction. The polymer and its derived hard carbon material were characterized by FTIR, 13C NMR, Raman, BET, and other characterization tools. The electrochemical properties of both materials as anode electrodes of lithium-ion batteries were investigated. Benefiting from the highly cross-linked skeleton and conjugated stru
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Jeon, Hyo Jin, Dong Ok Kim, Jea Sung Park, et al. "Synthesis of Hyper Crosslinked Polymer Particle Having Hydroxyl Group." Polymer Korea 35, no. 1 (2011): 66–71. http://dx.doi.org/10.7317/pk.2011.35.1.66.

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Nikoshvili, L., A. Bertova, E. Sulman, and L. Kiwi-Minsker. "Hyper-crosslinked Polystyrene as a Support for Development of Hydrogenation Catalysts: Influence of Porosity." Bulletin of Science and Practice 5, no. 12 (2019): 47–53. http://dx.doi.org/10.33619/2414-2948/49/05.

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This paper is devoted to the prospects for the use of hyper-crosslinked polystyrene as a support for the development of catalysts for selective hydrogenation of alkynols for synthesis of fragrant substances and fat-soluble vitamins E and K. Various types of hyper-crosslinked polystyrene, characterized by different porosity, were used for the synthesis of palladium catalysts by wet-impregnation of polymers with palladium acetate. It was shown that in the case of C5 alkynol, the pore structure of the polymers does not significantly affect the observed catalytic activity, whereas for C10 and C20
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Jia, Ziyan, Jiannan Pan, Chen Tian, and Daqiang Yuan. "Twisted molecule-based hyper-crosslinked porous polymers for rapid and efficient removal of organic micropollutants from water." RSC Advances 8, no. 64 (2018): 36812–18. http://dx.doi.org/10.1039/c8ra04792h.

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Быков, Алексей Владимирович, and Галина Николаевна Демиденко. "THERMAL STABILITY AND POROSITY OF HYPER-CROSSLINKED AROMATIC POLYMERS." Вестник Тверского государственного университета. Серия: Химия, no. 2(40) (June 6, 2020): 62–72. http://dx.doi.org/10.26456/vtchem2020.2.8.

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В работе методами сопряженной с масс-спектрометрией термогравиметрии, физической адсорбции азота, инфракрасной спектроскопии диффузного отражения и рентгенофотоэлектронной спектроскопии проведено исследование изменений пористости и состава функциональных групп полимера MN270 в температурном диапазоне от 30 до 600С. В ходе исследования показано, что при разогреве ненаполненного металлами полимера его микропористая структура рушится при температурах ниже 300С, в то время как разрушение, связанное с деструкцией и деполимеризацией самой полимерной матрицы, происходит при температурах выше 350С. Th
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Ramirez-Vidal, Pamela, Fabián Suárez-García, Rafael L. S. Canevesi, et al. "Irreversible deformation of hyper-crosslinked polymers after hydrogen adsorption." Journal of Colloid and Interface Science 605 (January 2022): 513–27. http://dx.doi.org/10.1016/j.jcis.2021.07.104.

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Meng, Bo, Haiying Li, Shannon M. Mahurin, Honglai Liu, and Sheng Dai. "Hyper-crosslinked cyclodextrin porous polymer: an efficient CO2 capturing material with tunable porosity." RSC Advances 6, no. 111 (2016): 110307–11. http://dx.doi.org/10.1039/c6ra18307g.

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Several cyclodextrin (CD)-based hyper-crosslinked porous polymers (HCPPs) were designed and synthesized for selective CO<sub>2</sub> adsorption and storage. A feasible way to tailor the porosity of the materials was also established.
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Li, Haiying, Bo Meng, Shannon M. Mahurin, et al. "Carbohydrate based hyper-crosslinked organic polymers with –OH functional groups for CO2 separation." Journal of Materials Chemistry A 3, no. 42 (2015): 20913–18. http://dx.doi.org/10.1039/c5ta03213j.

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A class of novel hyper-crosslinked microporous polymers, based on green and renewable carbohydrates, was synthesized for carbon capture and storage with high CO<sub>2</sub>/N<sub>2</sub> selectivity by hydrogen bonding and dipole–quadrupole interactions.
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Fayemiwo, Kehinde A., Goran T. Vladisavljević, Seyed Ali Nabavi, et al. "Nitrogen-rich hyper-crosslinked polymers for low-pressure CO2 capture." Chemical Engineering Journal 334 (February 2018): 2004–13. http://dx.doi.org/10.1016/j.cej.2017.11.106.

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Dissertations / Theses on the topic "Hyper-Crosslinked polymers"

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Ramirez, Vidal Pamela. "Matériaux nanoporeux à haute surface spécifique pour le stockage et la compression de l’hydrogène." Electronic Thesis or Diss., Université de Lorraine, 2021. http://www.theses.fr/2021LORR0178.

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Dans cette thèse, les performances d’adsorption d’hydrogène de trois familles de matériaux poreux à grande surface spécifique : les polymères hyper-réticulés (HCP), les charbons actifs commerciaux (CAC) et les réseaux organométalliques (MOF) ont été étudiées. Cette étude se compose de deux parties interconnectées : (i) l’évaluation expérimentale des performances de stockage de l’hydrogène dans les trois familles de matériaux ; et (ii) la modélisation du stockage de l’hydrogène dans les CAC et MOF à des températures comprises entre 77 et 273 K et à des pressions allant jusqu’à 14 MPa. La déform
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Books on the topic "Hyper-Crosslinked polymers"

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Korolev, G. V. Three-Dimensional Free-Radical Polymerization: Cross-Linked and Hyper-Branched Polymers. Springer Berlin Heidelberg, 2009.

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Book chapters on the topic "Hyper-Crosslinked polymers"

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Arcentales-Vera, Belén, Lisandra Bastidas, Moises Bustamante-Torres, Paul Maldonado Pinos, and Emilio Bucio. "Hyper-crosslinked Polymers." In Porous Polymer Science and Applications. CRC Press, 2022. http://dx.doi.org/10.1201/9781003169604-2.

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Conference papers on the topic "Hyper-Crosslinked polymers"

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Castaldo, R., V. Ambrogi, R. Avolio, et al. "Hyper-crosslinked resins filled with multiwalled carbon nanotubes." In VIII INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2016. http://dx.doi.org/10.1063/1.4949638.

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Song, Tao, Mohamed Ahdaya, Shuda Zhao, Yang Zhao, Thomas Schuman, and Baojun Bai. "Comprehensive Evaluation of a Novel Recrosslinkable Hyper Branched Preformed Particle Gels for the Conformance Control of High Temperature Reservoirs." In SPE Improved Oil Recovery Conference. SPE, 2022. http://dx.doi.org/10.2118/209451-ms.

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Abstract The existence of high conductivity features such as fractures, karst zones, and void space conduits can severely restrict the sweep efficiency of water or polymer flooding. Preformed particle gel (PPG), as a cost-effective technology, has been applied to control excessive water production. However, conventional PPG has limited plugging efficiency in high-temperature reservoirs with large fractures or void space conduits. After water breakthrough, gel particles can easily be washed out from the fractures due to the lack of particle-particle association and particle-rock adhesion. This
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