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20231120010457.0 |
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200620s2020 ne o 000 0 eng d |
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|a EBLCP
|b eng
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|d OPELS
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|a 019790710
|2 Uk
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|a 1159206478
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|a 9780128219584
|q (electronic bk.)
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|a 0128219580
|q (electronic bk.)
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|z 9780128219669
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|z 0128219661
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|a (OCoLC)1159164789
|z (OCoLC)1159206478
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|a QD383.F48
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|a 668.4/238
|2 23
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|a Opportunities for fluoropolymers :
|b synthesis, characterization, processing, simulation and recycling /
|c edited by Bruno Ameduri and Sergey Fomin.
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| 260 |
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|a Amsterdam :
|b Elsevier,
|c 2020.
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| 300 |
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|a 1 online resource (382 pages)
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| 336 |
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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1 |
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|a Progress in Fluorine Science series
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|a Print version record.
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|a Cover -- Title -- Copyright -- Contents -- Contributors -- About the editors -- Preface -- Chapter 1 -- Semi-fluorinated aromatic ether polymers via step-growth polymerization of fluoroalkenes -- 1 -- Introduction -- 2 -- Synthesis of perfluorocyclobutyl (pfcb) aromatic ether polymers from trifluorovinyl ether-bearing monomers -- 2.1 -- Synthesis of trifluorovinyl aromatic ethers (TFVE) -- 2.2 -- Synthesis of multifunctional trifluorovinyl ether (TFVE)-bearing monomers -- 2.3 -- PFCB containing monomers for classical polymerization
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|a 2.4 -- Postpolymerization modification on PFCB aryl ether polymers -- 2.5 -- Characterization of TFVE monomers and PFCB aromatic ether polymers -- 2.5.1 -- Infrared and Raman spectroscopy of TFVE monomers and PFCB aromatic ether polymers -- 2.5.2 -- Carbon nuclear magnetic resonance (NMR) spectroscopy -- 2.5.3 -- Fluorine NMR spectroscopy -- 2.5.4 -- Differential scanning calorimetry (DSC) -- 3 -- Synthesis and characterization of perfluorocycloalkenyl (PFCA) aromatic ether polymers -- 3.1 -- Select perfluorocycloalkenyl monomers used for synthesizing PFCA aromatic ether polymers
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|a 3.1.1 -- Direct step-growth polycondensation of perfluorocycloalkenes with bisphenols -- 3.1.2 -- Step-growth polycondensation of PFCA-end capped monomers bis(AA)-type with bisphenols -- 3.1.3 -- AB-type difunctional monomers in PFCA synthesis -- 3.1.4 -- PFCA as building block toward PFCA-enchained polymer synthesis -- 4 -- Synthesis and characterization of semi-fluorinated arylene vinylene ether (FAVE) polymers -- 4.1 -- Synthesis of FAVE polymers from the step-growth polycondensation of TFVE monomers and bisphenols -- 4.1.1 -- Direct step-growth polycondensation of TFVE and bisphenols
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|a 4.1.2 -- Step-growth polycondensation of TFVE- and hydroxyl-group containing oligomers -- 4.1.3 -- Postpolymerization modification of FAVE polymers -- 4.1.4 -- Enchainment of chromophoric units in FAVE polymers -- 5 -- Conclusion -- Abbreviations -- References -- CHAPTER 2 -- Iodine transfer emulsion polymerizations of vinylidene fluoride -- 1 -- Introduction -- 2 -- Results and discussion -- 2.1 -- Experimental considerations -- 2.2 -- Pressure impact on VDF ITP in emulsion -- 2.3 -- Impact of CTA structure and concentration on particle size distributions -- 3 -- Conclusions -- References
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|a Chapter 3 -- Fluorinated initiators, mediators, and solvents in controlled radical polymerization -- 1 -- Introduction: general aspects of controlled radical polymerization -- 2 -- Fluorinated agents in CRP -- 2.1 -- Fluorinated iniferters and chain transfer agents (for RAFT) -- 2.2 -- Fluorinated alkoxyamines and nitroxides for nitroxide mediated polymerization -- 2.3 -- Fluorinated alkyl halides and ligands for ATRP -- 3 -- Fluorine-containing macroinitiators -- 4 -- Fluorinated solvents -- 5 -- Conclusion and outlooks -- 6 -- Acknowledgments -- References
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| 505 |
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|a Chapter 4 -- Specifics of the Mn2(CO)10 photomediated synthesis of PVDF block copolymers
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| 650 |
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|a Fluoropolymers.
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| 650 |
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7 |
|a Fluoropolymers
|2 fast
|0 (OCoLC)fst00928184
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| 700 |
1 |
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|a Am�eduri, B.
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| 700 |
1 |
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|a Fomin, Sergey.
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| 776 |
0 |
8 |
|i Print version:
|a Ameduri, Bruno.
|t Opportunities for Fluoropolymers : Synthesis, Characterization, Processing, Simulation and Recycling.
|d San Diego : Elsevier, �2020
|z 9780128219669
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| 830 |
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0 |
|a Progress in fluorine science series.
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| 856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780128219669
|z Texto completo
|
