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Cation initiating

CINNAMICACID,CINNAMALDEHYDEANDCINNAMYLALCOHOL] (Vol6) -as polymerization initiator [INITIATORS - CATIONIC INITIATORS] (Vol 14)... [Pg.220]

One product is poly(2-ethyl-2-oxa2oline) (PEOX). It is prepared by the ring-opening polymerization of 2-ethyl-2-oxazoline (19) with a cationic initiator (48) (eq. 6). [Pg.320]

Since the discovery of living cationic systems, cationic polymerization has progressed to a new stage where the synthesis of designed materials is now possible. The rapid advances in this field will lead to useful new polymeric materials and processes that will greatiy increase the economic impact of cationic initiation. [Pg.246]

Higher a-olefins can also be polymerized with cationic initiators to fiquid oligomeric materials with isomerized stmctures. These fiquids are manufactured commercially and used as lubricating oils. [Pg.425]

Trichloromethanesulfenyl chloride can be added across double bonds under either free-radical or cationic-initiated conditions (55,56) ... [Pg.132]

VEs such as MVE polymerize slowly in the presence of free-radical initiators to form low mol wt products of no commercial importance (9). Examples of anionic polymerization are unknown, whereas cationic initiation promotes rapid polymerization to high mol wt polymers in excellent yield and has been extensively studied (10). [Pg.514]

In the presence of cationic initiators, the possibiUty for loss of pendant ether groups to form free alcohol is another side reaction that usually results in color formation because of the highly conjugated products formed. [Pg.515]

Radiation curing of epoxies with cationic initiators is well known [20—28]. UV-visible light has been the predominant radiation source the process has been limited to thin coatings due to the low penetration of the visible-UV light [22,23], Thermal and mechanical properties of these materials are low and the curing is incomplete. Several studies have shown that commercially available epoxies with various cationic initiators can be polymerized with EB curing [20,29-34]. [Pg.1022]

An analogous mechanism should also produce polymers on irradiation of epoxies. Crivello s recent mechanistic suggestions [29] are consistent with the mechanisms given above. One can conclude that radiation-induced polymerization of epoxies can proceed via several mechanisms. However, further work is needed to determine the relative contributions of the different mechanisms, which might vary from one epoxy to another. As part of the Interfacial Properties of Electron Beam Cured Composites CRADA [37], an in-depth study of the curing mechanism for the cationic-initiated epoxy polymerization is being undertaken. [Pg.1023]

Materials and additives that are chemically basic in nature have a detrimental effect on the curing of cationic-initiated epoxy systems. These substances can either stop the curing mechanism completely or produce under-cured polymers. Therefore such additives as amines or imides that are known to be adhesion promoters cannot be used in the EB-curable epoxy adhesive formulations. [Pg.1023]

Studies on the dimerization and hydrogenation of olefins with transition metal catalysts in acidic chloroaluminate(III) ionic liquids report the formation of higher molecular weight fractions consistent with cationic initiation [L7, 20, 27, 28]. These... [Pg.320]

Cationic polymerizations work better when the monomers possess an electron-donating group that stabilizes the intermediate carbocation. For example, isobutylene produces a stable carbocation, and usually copolymerizes with a small amount of isoprene using cationic initiators. The product polymer is a synthetic rubber widely used for tire inner tubes ... [Pg.307]

Cationic initiators can also polymerize aldehydes. For example, BF3 helps produce commercial polymers of formaldehyde. The resulting polymer, a polyacetal, is an important thermoplastic (Chapter 12) ... [Pg.307]

Problem 31.6 Draw the structure of an alternating segment of butyl rubber, a copolymer of iso-prene (2-methyl-],3-butadiene) and isobutylene (2-methylpropene) prepared using a cationic initiator. [Pg.1212]


See other pages where Cation initiating is mentioned: [Pg.5]    [Pg.129]    [Pg.144]    [Pg.175]    [Pg.246]    [Pg.302]    [Pg.423]    [Pg.513]    [Pg.513]    [Pg.528]    [Pg.529]    [Pg.529]    [Pg.576]    [Pg.747]    [Pg.748]    [Pg.767]    [Pg.778]    [Pg.857]    [Pg.938]    [Pg.1012]    [Pg.1054]    [Pg.58]    [Pg.244]    [Pg.244]    [Pg.244]    [Pg.245]    [Pg.246]    [Pg.430]    [Pg.432]    [Pg.514]    [Pg.525]    [Pg.1022]    [Pg.1022]    [Pg.1034]    [Pg.424]    [Pg.541]   
See also in sourсe #XX -- [ Pg.124 , Pg.126 , Pg.128 ]

See also in sourсe #XX -- [ Pg.124 , Pg.126 , Pg.128 ]




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Acids in Cationic Initiations

Alkyls in Initiations of Cationic Polymerizations

Allylic cations initiators

Cation-exchange resins initiator

Cation-initiated reaction

Cation-pool Initiated Polymerization of Vinyl Ethers Using a Microflow System

Cation-pool initiated

Cation-pool initiated microsystem

Cation-pool initiated polymerization

Cationic Polymerization with Lewis Acids as Initiators

Cationic chain polymerization initiation

Cationic coordination polymerization initiation

Cationic heterocyclic polymerization Initiation mechanism

Cationic initiation

Cationic initiation

Cationic initiators

Cationic initiators

Cationic initiators from

Cationic initiators from anionic leaving groups

Cationic initiators from electrophilic

Cationic initiators from olefins

Cationic initiators vinyl ether polymerization

Cationic initiators, ring-opening polymerization

Cationic polymerization CF3SO3H initiation

Cationic polymerization Initiators properties

Cationic polymerization Initiators structure

Cationic polymerization cation-pool initiation

Cationic polymerization initiation

Cationic polymerization protonic acid initiation

Cationic radical initiators

Cationic-Initiated MBFTs

Cationic-initiated chain polymerization

Cationic-initiated chain polymerization polyisobutylene

Cationic-initiated polymerization

Cycloaddition reactions radical cation-initiated

Epichlorohydrin cationic polymerization mechanism initiation

Formation of initiating cation

Ideal living cationic initiation

Immonium cations initiators

Initiation in cationic polymerization

Initiation of cationic polymerization

Initiation with triphenylmethyl cation

Initiator cationic polymerization

Initiator of cationic polymerization

Initiator, anionic cationic

Initiators Friedel-Crafts, cationic

Initiators for cationic polymerization

Initiators in cationic polymerization

Initiators, anionic cationic polymerization

Lewis acids cationic initiators

Photo-initiated cationic polymerization

Photo-initiated cationic polymerization epoxides

Photoinitiated cationic polymerization Bronsted acid Initiation

Polymerization, cationic macromonomer initiators

Polymerization, initiators cationic type

Polymerization, “cation pool initiator

Radiation-induced cationic initiation

Ring-Opening Polymerization of Dilactide with Cationic Initiators in Solution

Theoretical Attempts at Improving Initiators for Cationic Polymerisation of Alkenes

Thermally Initiated cationic

Thermally Initiated cationic Initiation

Thermally Initiated cationic arylation

Thermally Initiated cationic polymerization

Thermally Initiated cationic temperatures

Thermally Initiated cationic with free radicals

Triphenylmethyl cation, initiation

Vinyl ethers, “cation pool polymerization initiator

Vinylindoles, cycloaddition radical cation-initiated

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