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Relevant bibliographies by topics / Cationic polymerisation

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Academic literature on the topic 'Cationic polymerisation'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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Journal articles on the topic "Cationic polymerisation"

1

Williams, M., N. J. W. Penfold, and S. P. Armes. "Cationic and reactive primary amine-stabilised nanoparticles via RAFT aqueous dispersion polymerisation." Polymer Chemistry 7, no. 2 (2016): 384–93. http://dx.doi.org/10.1039/c5py01577d.

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Synthesis of cationic reactive primary amine-functionalized diblock copolymer nano-objects via polymerisation-induced self-assembly (PISA) using a RAFT aqueous dispersion polymerisation formulation is reported.

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Tran, Anh Dung, Thomas Koch, Robert Liska, and Patrick Knaack. "Radical-induced cationic frontal polymerisation for prepreg technology." Monatshefte für Chemie - Chemical Monthly 152, no. 1 (2021): 151–65. http://dx.doi.org/10.1007/s00706-020-02726-y.

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AbstractIn this study, a new type of prepreg technology has been established using a dual curing system consisting of 1,6-hexanediol diacrylate (HDDA) and frontally polymerisable components based on the epoxide resin. The study of the polymerisation of HDDA revealed (tert-butylcyclohexyl)peroxydicarbonate (BCPC) as the most suitable radical thermal initiator. The presence of BCPC resulted in a fast radical polymerisation of HDDA and no cationic ring-opening reaction of the epoxy, which was observed by monitoring the double bond and epoxy group conversion in real time-NIR rheology measurement.

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Irawan, Yan, Ika Juliana, and Emil Budianto. "Synthesis of palm oil based polymeric ester through cationic addition polymerisation method." Malaysian Journal of Fundamental and Applied Sciences 17, no. 1 (2021): 16–19. http://dx.doi.org/10.11113/mjfas.v17n1.1524.

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In this study, the synthesis of palm oil-based polymeric ester for application as a polymeric surfactant was carried out by a cationic addition polymerisation method through two steps. The initial step is a synthesis of fatty acid methyl esters oleate (FAMEO) through esterification reaction between oleic acid and methanol. The optimum conditions of the esterification reaction were carried out at a temperature of 70–80oC for 4 hours with the addition of 1wt% sulfuric acid as a catalyst. The molar ratio between oleic acid and methanol was 1:3. FAMEO was analysed using GCMS to determine the methy

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4

Plesch, Peter H. "Pseudo-cationic polymerisation after 24 years." Makromolekulare Chemie. Macromolecular Symposia 13-14, no. 1 (1988): 375–87. http://dx.doi.org/10.1002/masy.19880130126.

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5

Decker, Christian, Danielle Decker, Trieu Nguyen Thi Viet, and Hien Le Xuan. "Photoinitiated cationic polymerisation of multifunctional systems." Macromolecular Symposia 102, no. 1 (1996): 63–71. http://dx.doi.org/10.1002/masy.19961020110.

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6

Grace, James L., Johnny X. Huang, Soon-Ee Cheah, et al. "Antibacterial low molecular weight cationic polymers: dissecting the contribution of hydrophobicity, chain length and charge to activity." RSC Advances 6, no. 19 (2016): 15469–77. http://dx.doi.org/10.1039/c5ra24361k.

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7

Gomes, Clara S. B., Alejandro F. G. Ribeiro, Anabela C. Fernandes та ін. "Reactivity of cationic α-diimine cyclopentadienyl nickel complexes towards AlEt2Cl: synthesis, characterisation and ethylene polymerisation". Catalysis Science & Technology 7, № 14 (2017): 3128–42. http://dx.doi.org/10.1039/c7cy00875a.

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8

Williams, M., N. J. W. Penfold, J. R. Lovett, et al. "Bespoke cationic nano-objects via RAFT aqueous dispersion polymerisation." Polymer Chemistry 7, no. 23 (2016): 3864–73. http://dx.doi.org/10.1039/c6py00696e.

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9

Camerlynck, Stephanie, Peter A. G. Cormack, and David C. Sherrington. "Synthesis of branched polystyrenes via cationic polymerisation." European Polymer Journal 42, no. 12 (2006): 3286–93. http://dx.doi.org/10.1016/j.eurpolymj.2006.08.019.

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10

Nuyken, Oskar, Stephen D. Pask, Axel Vischer, and Michael Walter. "Telechelics from methyl propene via cationic polymerisation." Makromolekulare Chemie. Macromolecular Symposia 3, no. 1 (1986): 129–52. http://dx.doi.org/10.1002/masy.19860030111.

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Dissertations / Theses on the topic "Cationic polymerisation"

1

Tranter, Kenneth Shaun. "Remote cationic curing." Thesis, City University London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340378.

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Sarker, Prodip Kumar. "Reactive polymers by ab initio cationic polymerisation." Thesis, University of Sheffield, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400001.

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Forder, Clive. "Water-soluble block copolymers via living cationic polymerisation." Thesis, University of Sussex, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318608.

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Yeates, Terence. "Synthesis and solution of polystyrene-block-polyisobutene copolymers." Thesis, University of Manchester, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.237269.

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Penfold, Nicholas. "Synthesis of cationic nanoparticles via polymerisation-induced self-assembly." Thesis, University of Sheffield, 2017. http://etheses.whiterose.ac.uk/18126/.

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Norström, Emelie. "Terpenes as renewable monomers for biobased materials." Thesis, KTH, Skolan för kemivetenskap (CHE), 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-49875.

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With the ambition to decrease the utilization of fossil fuels, a development of those raw materials that today only are seen as waste products is necessary. One of those waste products is turpentine. Turpentine is the largest natural source of terpenes in the world today. The main components are the terpenes α-pinene, β-pinene and 3-carene. In this project, different polymerisation techniques have been evaluated to polymerise limonene with the aim to make a material out of the green raw material, turpentine. Limonene is a terpene that can be found in turpentine. It has a planar structure and

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Shorrock, Jennifer Kate. "Cationic polymerisation of alicene monomers by silica-supported aluminium chloride." Thesis, University of York, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.250624.

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Krishnamoorthy, Mahentha. "Developing cationic nanoparticles for gene delivery." Thesis, Queen Mary, University of London, 2016. http://qmro.qmul.ac.uk/xmlui/handle/123456789/23193.

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Gene delivery can potentially treat acquired and genetic diseases such as cystic fibrosis, haemophilia and cancer. Non-viral gene delivery vectors are attractive candidates over viral vectors such as recombinant viruses, due to their lower cytotoxicity and immunogenicity, despite significantly lower transfection efficiencies. To improve efficiency of non-viral vectors, the investigation of the various parameters influencing DNA transfection is essential. The present study developed a versatile gene delivery system with tailored physicochemical and biological properties. The system used polymer

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DesaÌ„iÌ„, Hemanta. "Studies of the cationic polymerisation of vinylic energetic cyclic ether monomers." Thesis, Aston University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294631.

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Lang, Weihong. "Synthesis of oligo (vinyl ether)s in ab initio cationic polymerisation." Thesis, University of Sheffield, 2002. http://etheses.whiterose.ac.uk/10205/.

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Terminally functionalised oligo(vinyl ether)s were produced in ab initio cationic polymerisations. Various polymerisations and chain end functionalisation systems were investigated. MALDI-TOF mass spectrometry was applied to analyse the obtained oligomers and thus the polymerisation and chain end functionalisation process. Oligo(isobutyl vinyl ether), also oligo(ethyl vinyl ether) and oligo(methyl vinyl ether) were synthesised in cationic polymerisation. Silyl enol ethers were added to the polymerisation as end-capping agents before initiations and they compete with monomer to cap the carbocat

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Books on the topic "Cationic polymerisation"

1

Lancaster, Simon John. Cationic group IV metal alkyls as polymerisation catalysts. University of East Anglia, 1992.

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2

Desai, Hemant. Studies of the cationic polymerisation of vinylic and energetic cyclic ether monomers. Aston University. Department of Chemical Engineering and Applied Chemistry, 1995.

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3

Gandini, A., and H. Cheradame. Cationic Polymerisation: Initiation Processes with Alkenyl Monomers. Springer, 2013.

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4

Penczek, S. Cationic Ring-Opening Polymerization: Part 2, Synthetic Applications (Advances in Polymer Science, Vol 68/69). Springer, 1985.

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5

Plesch, P. H. Developments in the Theory of Cationoid Polymerisations. Smithers Rapra Technology, 2002.

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Book chapters on the topic "Cationic polymerisation"

1

Timpe, H. J. "Kinetic Aspects of Light-Induced Cationic Polymerisation." In Radiation Curing in Polymer Science and Technology—Volume II. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1876-7_11.

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2

"Chain Polymerisation." In Fundamentals of Inorganic and Organometallic Polymer Science. Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781837672325-00064.

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Chain polymerisation involves the reaction of unsaturated monomers to form polymers. Compared to step polymerisation (discussed in Chapter 2), chain polymerisation is the pre-eminent technique to synthesise high molecular weight polymers, particularly transition metal-containing polymers. The techniques can be classified into radical, cationic, anionic, ring-opening, and ring-opening metastasis polymerisations depending on the mechanism of initiation and propagation or the structure of the monomer. By the end of the chapter, we expect the student to understand important mechanistic and kinetic

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3

"7. Polyether polyols by cationic polymerisation processes." In [Set Polyols for Polyurethanes, Volume 1+2]. De Gruyter, 2019. http://dx.doi.org/10.1515/9783110644104-007.

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4

FRENKING, GERNOT, HIROSHI KATO, and KENICHI FUKUI. "An MO-Theoretical Treatment of the Cationic Ring-Opening Polymerisation.: I. Ethylene Oxide." In Frontier Orbitals and Reaction Paths. WORLD SCIENTIFIC, 1997. http://dx.doi.org/10.1142/9789812795847_0031.

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Conference papers on the topic "Cationic polymerisation"

1

Gaspar, Jorge, and Paulo Jorge Ba´rtolo. "Metallic Stereolithography." In ASME 2008 9th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2008. http://dx.doi.org/10.1115/esda2008-59418.

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The rising of consumers’ demands and an ever increasing pressure of international markets imposed a deep change in the product development process to respond to an increasing product complexity and higher quality, as well to the need to promptly introduce products into the market. Stereolithography plays an important role on this new product development context. This technology produces models for thermosetting resins through a polymerisation process that transforms liquid resins into solid materials. In this work, a new route to produce metallic parts through stereolithography is explored. Th

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2

You, J., X. Tang, F. Zhang, et al. "Quantitative studies on the microstructures of ternary CaO-Al2O3-SiO2 glasses, melts and correlation with their high-temperature viscosities." In 12th International Conference of Molten Slags, Fluxes and Salts (MOLTEN 2024) Proceedings. Australasian Institute of Mining and Metallurgy (AusIMM), 2024. http://dx.doi.org/10.62053/lnvg1782.

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Microstructure of CaO-SiO2-based glassy samples with various Al2O3 contents were examined quantitatively by Raman spectroscopy and 27Al MAS NMR (magic-angle spinning nuclear magnetic resonance). Sequence of multiple cluster models of aluminosilicate system modified with Ca2+ and Na+ cations have been designed, and Raman spectra simulation were carried out after geometric optimisation by quantum chemistry (QC) ab initio calculation. The functional relationship between Raman scattering cross-section (RSCS) and stress index of silicon-oxygen tetrahedron (SIT) for aluminosilicates was established,

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