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Polymeric triblock

The above polymeric triblocks can be applied as dispersants, whereby the assumption is made that the hydrophobic PPO chain resides at the hydrophobic surface, leaving the two PEO chains dangling in aqueous solution and hence providing steric repulsion. Although these triblock polymeric surfactants have been widely used in various appHcations suspensions, some doubt has arisen as to how effective these can be. It is generally accepted that the PPO chain is not sufficiently hydrophobic to provide a strong anchor to a hydrophobic surface. [Pg.51]

The above polymeric triblocks can be applied as emulsifiers or dispersants, whereby the assumption is made that the hydrophobic PPO chain resides at the hydrophobic surface, leaving the two PEO chains dangling in aqueous solution and hence providing steric repulsion. [Pg.347]

Thermoplastic elastomers have the important advantage over conventional elastomers that there is no need for the additional chemical crosslinking reaction and fabrication is achieved in the same way as for thermoplastics. However, only certain polymerization methods can be used to synthesis block copolymers — primarily living anionic chain polymerization and certain step polymerizations. Triblock copolymers are produced by living anionic polymerization by sequential addition of different momomer charges to a living anionic system, for example, a styrene-isoprene-styrene is synthesized by the sequence... [Pg.14]

Several examples of block and graft copolymers may be quoted. Triblock polymeric surfactants [ Pluronics (BASF) or Synperonic PE (ICI)] - two poly-A blocks of PEO and one block poly-B of poly(propylene oxide) (PPO) several chain lengths of PEO and PPO are available. Triblocks of PPO-PEO-PEO (inverse Pluronics ) are also available. Polymeric triblock surfactants can be applied as emulsifiers and dispersants. The hydrophobic PPO chain resides at the hydrophobic surface, leaving the two PEO chains dangling in aqueous solution (providing steric stabilisation). [Pg.95]

Butadiene copolymers are mainly prepared to yield mbbers (see Styrene-butadiene rubber). Many commercially significant latex paints are based on styrene—butadiene copolymers (see Coatings Paint). In latex paint the weight ratio S B is usually 60 40 with high conversion. Most of the block copolymers prepared by anionic catalysts, eg, butyUithium, are also elastomers. However, some of these block copolymers are thermoplastic mbbers, which behave like cross-linked mbbers at room temperature but show regular thermoplastic flow at elevated temperatures (45,46). Diblock (styrene—butadiene (SB)) and triblock (styrene—butadiene—styrene (SBS)) copolymers are commercially available. Typically, they are blended with PS to achieve a desirable property, eg, improved clarity/flexibiHty (see Polymerblends) (46). These block copolymers represent a class of new and interesting polymeric materials (47,48). Of particular interest are their morphologies (49—52), solution properties (53,54), and mechanical behavior (55,56). [Pg.507]

Ring-Opening Metathesis Polymerization. Several new titanacyclobutanes have been shown to initiate living ring-opening metathesis polymerization (ROMP) systems. These have been used to make diblock and triblock copolymers of norbomene [498-66-8] (N) and its derivatives (eg, dicyclopentadiene [77-73-6] (D)) (Fig. 2) (41). [Pg.181]

Thermoplastic Elastomers. These represent a whole class of synthetic elastomers, developed siace the 1960s, that ate permanently and reversibly thermoplastic, but behave as cross-linked networks at ambient temperature. One of the first was the triblock copolymer of the polystyrene—polybutadiene—polystyrene type (SheU s Kraton) prepared by anionic polymerization with organoHthium initiator. The stmcture and morphology is shown schematically in Figure 3. The incompatibiHty of the polystyrene and polybutadiene blocks leads to a dispersion of the spherical polystyrene domains (ca 20—30 nm) in the mbbery matrix of polybutadiene. Since each polybutadiene chain is anchored at both ends to a polystyrene domain, a network results. However, at elevated temperatures where the polystyrene softens, the elastomer can be molded like any thermoplastic, yet behaves much like a vulcanized mbber on cooling (see Elastomers, synthetic-thermoplastic elastomers). [Pg.471]

Block copolymer chemistry and architecture is well described in polymer textbooks and monographs [40]. The block copolymers of PSA interest consist of anionically polymerized styrene-isoprene or styrene-butadiene diblocks usually terminating with a second styrene block to form an SIS or SBS triblock, or terminating at a central nucleus to form a radial or star polymer (SI) . Representative structures are shown in Fig. 5. For most PSA formulations the softer SIS is preferred over SBS. In many respects, SIS may be treated as a thermoplastic, thermoprocessible natural rubber with a somewhat higher modulus due to filler effect of the polystyrene fraction. Two longer reviews [41,42] of styrenic block copolymer PSAs have been published. [Pg.479]

The earliest SIS block copolymers used in PSAs were nominally 15 wt% styrene, with an overall molecular weight on the order of 200,000 Da. The preparation by living anionic polymerization starts with the formation of polystyryl lithium, followed by isoprene addition to form the diblock anion, which is then coupled with a difunctional agent, such as 1,2-dibromoethane to form the triblock (Fig. 5a, path i). Some diblock material is inherently present in the final polymer due to inefficient coupling. The diblock is compatible with the triblock and acts... [Pg.480]

Sequential one styrene block is polymerized, then the mid-block monomer is added and polymerized, then more styrene is added and the second styrene block polymerized. This process is used to produce 100% triblock rubbers, for maximum strength [5]. Termination is commonly with alcohols, which produces a lithium alkoxide salt as the by-product. [Pg.713]

The preparation of ABA triblock polymers requires use of a telechelie bisthiol prepared by termination of anionic polymerization initiated by a difunctional initiator. The relative yields of homopolymer, di- and triblock obtained in these experiments depend critically on conversion.273... [Pg.388]

Poly(dimethyl siloxanc) with vinyl or hydrosilanc (Si-H) chain ends have been converted to ATRP initiator ends e.g. Scheme 9.62) by hydrosilylalion, Bis-functional dimethyl siloxane polymers prepared in this way were used in polymerizations of S, MA, tsobornyl acrylate and BA to form ABA triblock copolymers. [Pg.546]

Polystyrene-Woc -polysulfone-/ /oc -polystyrene and poly(butyl acrylate)-Woc -polysulfone-/ /oc -poly(butyl acrylate) triblock copolymers were prepared using a macroinitiator.214 The hydroxyl-terminated polysulfone was allowed to react with 2-bromopropionyl bromide, an atomic transfer radical polymerization (ATRP) initiator, in the presence of pyridine. The modified macroinitiator could initiate die styrene polymerization under controlled conditions. [Pg.359]

Bifunctional initiators are sometimes needed e.g., for the synthesis of triblock copolymers, networks, or a,co-difunctional macromolecules. Whenever it is possible to carry out the polymerization in a polar solvent no major difficulty is involved, as bifunctional initiators covering a wide range of nucleophilicities are available (Table 2). [Pg.151]

Vinyl copolymers contain mers from two or more vinyl monomers. Most common are random copolymers that are formed when the monomers polymerize simultaneously. They can be made by most polymerization mechanisms. Block copolymers are formed by reacting one monomer to completion and then replacing it with a different monomer that continues to add to the same polymer chain. The polymerization of a diblock copolymer stops at this point. Triblock and multiblock polymers continue the polymerization with additional monomer depletion and replenishment steps. The polymer chain must retain its ability to grow throughout the process. This is possible for a few polymerization mechanisms that give living polymers. [Pg.470]

Linear triblock copolymers of the type styrene-butadiene-styrene (SBS) and styrene-isoprene-styrene (SIS) are produced commercially by anionic polymerization through sequential addition of monomers in the reaction chamber [10] as shown below ... [Pg.107]

Recently, Cohn and Salomon synthesized and characterized a series of PLCL thermoplastic bioelastomers by two-step synthesis procedure. First, ring-opening polymerization of L-lactide initiated by the hydroxyl terminal groups of the PCL chain. Second, chain extension polymerization of these PLA-PCL-PLA triblocks initiated by the hexamethylene diisocyanate (HDl). [Pg.229]

Based on the synthesis of polyphosphazenes and of diblock copolyphosp-hazenes by the living cationic polymerization of phosphoranimines [237,241], the triblock poly(phosphazene-ethylene oxide) copolymer XVIII was synthesized by Allcock [223]. [Pg.212]

The anionic method of polymerization is most useful for the synthesis of low molecular weight hydroxy-terminated oligomers and polymers that are to be further processed. For example, the treatment of hydroxy-terminated oligomers with isocyanates has been used to obtain polyester-urethanes (9,20), while triblock copolymers (PCL-PEG-PCL) are prepared by initiating the polymerization of e-caprolactone with the disodium alcoholate from polyethylene glycol (26). [Pg.73]

A related strategy has been employed to prepare a triblock copolymer of styrene and e-caprolactone by initiating the polymerization... [Pg.73]

The living nature of PCL obtained in the presence of Zn(OAl-(OPri)2)2 has been used to prepare both di- and triblock copolymers of e-caprolactone and lactic acid (42,43). Treatment of the initial living PCL with dilactide afforded a PCL-PLA diblock with M /Mn = 1.12, with each block length determined by the proportions of the reactants, i.e., the ratio of [monomer]/[Zn]. While the living diblock copolymer continued to initiate dilactide polymerization, it failed to initiate e-caprolactone polymerization. To obtain a PCL-PLA-PCL triblock, it was necessary to treat the living PCL-PLA-OAIR2 intermediate with ethylene oxide, then activate the hydroxy-terminated PCL-PLA-(OCH2CH2)nOH with a modified Teyssie catalyst (Fig. 5). [Pg.78]

Brzezinska KR, Deming TJ (2001) Synthesis of ABA triblock copolymers via acyclic diene metathesis polymerization and living polymerization of alpha-amino acid-N-carboxyanhy-drides. Macromolecules 34 4348 354... [Pg.25]

Statistical and block copolymers based on ethylene oxide (EO) and propylene oxide (PO) are important precursors of polyurethanes. Their detailed chemical structure, that is, the chemical composition, block length, and molar mass of the individual blocks may be decisive for the properties of the final product. For triblock copolymers HO (EO) (PO)m(EO) OH, the detailed analysis relates to the determination of the total molar mass and the degrees of polymerization of the inner PPO block (m) and the outer PEO blocks (n). [Pg.403]


See other pages where Polymeric triblock is mentioned: [Pg.78]    [Pg.92]    [Pg.194]    [Pg.78]    [Pg.92]    [Pg.194]    [Pg.239]    [Pg.467]    [Pg.183]    [Pg.472]    [Pg.130]    [Pg.481]    [Pg.500]    [Pg.309]    [Pg.742]    [Pg.759]    [Pg.545]    [Pg.547]    [Pg.616]    [Pg.6]    [Pg.29]    [Pg.69]    [Pg.107]    [Pg.108]    [Pg.141]    [Pg.202]    [Pg.300]    [Pg.880]    [Pg.8]    [Pg.15]   
See also in sourсe #XX -- [ Pg.78 ]




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