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Polymer block-copolymer

Finally, we briefly mention interactions due to adsorbing polymers. Block copolymers, witli one block strongly adsorbing to tire particles, have already been mentioned above. Flere, we focus on homopolymers tliat adsorb moderately strongly to tire particles. If tliis can be done such tliat a high surface coverage is achieved, tire adsorbed polymer layer may again produce a steric stabilization between tire particles. [Pg.2680]

Kennedy and co-workers 2 117) used the changing effect of the initiation ability of the Lewis acids according to Eq. (17) and the termination tendency of the anion formed according to Eq. (18) in order to obtain telechelic polymers , block copolymers and graft copolymers in a controlled manner. Quantum chemical calculations provide the possibility to discuss structural influences which work on the equilibrium Eq. (19) and therefore on the stability of the two adjacent ions. [Pg.207]

Block copolymers with organic polymers Block copolymers with polysiloxanes Comb copolymers Fuel cell membranes ROMP polymerizations Azide coupling to organic polymers ADMET polymerizations... [Pg.146]

Synthesis of Well Defined Copolymer Structures Starting from Ozonized Polymers Block Copolymers, Graft Copolymers, Telechelic Oligomers... [Pg.58]

Cationic polymerizations are among the most important synthetic methods in polymer chemistry. They are used to prepare a variety of commodity and specialty polymers. More recently, controlled cationic polymerizations have been used to synthesize novel functional polymers, block copolymers, and macromolecules with new topologies. The importance of reactions involving cationic active species is continuously increasing, and was recently recognized by the awarding of the 1994 Nobel Prize in Chemistry to George Olah. [Pg.775]

Keywords Hydrogen bonding Polymers Block copolymers Self-assembly Tunability Responsivity... [Pg.114]

The properties of silicones can be modified by combination with organic polymers. Block copolymers of poly(organo-siloxanes) and poly(ethers) as well as thermoplastic-modified silicones are industrially important, in addition to silicone combination resins. [Pg.323]

System 2 By application of an Impact modifier containing groups which are reactive to the accelerator ("solution I"), graft polymers (block copolymer) can be formed. [Pg.184]

One of the most distinguishable characteristics of the metal-catalyzed living radical polymerization is that it affords polymers with controlled molecular weights and narrow MWDs from a wide variety of monomers under mild conditions even in the presence of a protic compound such as water. This permits the synthesis of a vast number of polymers with controlled structures such as end-functionalized polymers, block copolymers, star polymers, etc., where they are widely varied in comparison with those obtained by other living polymerizations. This is primarily due to the tolerance to various functional groups and the polymerizability/controllability of various vinyl monomers as mentioned above. [Pg.483]

Polymer-colloids refer to particles consisting of a solid core surrounded by a polymeric corona. Tills broad class of materials encompasses systems as different as star polymers, block copolymer micelles, and grafted particles. [Pg.126]

Small-angle X-ray scattering techniques provide a route to information at a larger scale, particularly in multi-phase materials such as semi-crystalline polymers, block copolymers, and blends. Quantitative details on crystalline lamellar size or on preferred orientation are just two examples of the structural parameters which can be obtained using this powerful technique.2" 2>243... [Pg.25]

The composite systems studied by Takayanagi et al. (1980) used the polyaramides poly(p-phenylene terephthamide), PPDT, or pol.y-p-benzamide (PBA) as the reinforcing component with nylon 6 or nylon 66 as the ductile matrix polymer. Block copolymers of one of the aromatic polyamides with one of the nylon polymers were also evaluated. The blends were prepared by extruding the sulfuric acid solutions of polymers into a... [Pg.272]

The International Union of Pure and Applied Chemistry (lUPAC) formed a Subcommission on Nomenclature of Macromolecules in 1952 and has proceeded to study various topics related to cyclic polymers, blends, composites, cross-linked polymers, block copolymers, etc. lUPAC periodically reports its decisions regarding nomenclature (1, 7, and ). Even so, these rules have not been generally accepted for common polymers by the majority of those in polymer science. [Pg.41]

Random Copolymers Alternating Copolymers Graft Polymers Block Copolymers... [Pg.219]

ZYLAR series of alloys of brittle polymer, ductile polymer and rubbery polymer are available from Novacor Chemicals, Inc. The components are brittle polymer, styrene (70 wt%) and methyl methacrylate (30 wt%) (Novacor s NAS30) ductile polymer, block copolymer derived from styrene (75 wt%) and butadiene (25 wt%) and rubbery polymer, a tapered polymer derived from styrene (43 wt%) and butadiene (57 wt%). No specific gamma stabilizers were added to these polymer alloys. [Pg.848]

AFM is widely used in the analysis of polymer surfaces, such as morphology and molecidar structure of crystalline and oriented polymers, block copolymers, and polymer blends. The example shown in Figure 10.13(b) is the AFM three-dimensional smface image of the fracture surface of a composite. A lamellar structure is clearly observed, with periodicity of about 200 nm, comparable to values obtained from the SEM micrographs [Figure 10.13(a)]. [Pg.276]

There have been other types of approaches also for the synthesis of hybrid polymers. Block copolymers containing polysiloxane segments and polyphosphazene segments have been synthesized by the reaction of hydride-terminated polysiloxane H-[Si(Me2)-0]n-SiMe2H with the telechelic polyphosphazene containing an amino end-group (Fig. 6.28) [33]. [Pg.240]

The polymers may be introduced into the chromatographic column as powders of appropriate particle size, as in the case of melting transition, thus avoiding the preceding dissolution of samples. The retention diagrams recorded with powders of poly(vinyl chloride) [153], polyacrylonitrile [200] and polybutadiene [207] assume exactly the shape in Figure 5.13. This aspect is useful in the case of semi-crystalline polymers, block copolymers with incompatible blocks, and fibres [176] because it makes possible the study of the effect of thermal treatment on the transitions. [Pg.170]

In these two decades remarkable progress has been made in the development of excellent catalysts for living and stereospecific acetylene polymerizations (10,26-28). The r-conjugated polymers prepared by the sequential polsrmerization are strictly limited to polyacetylenes, except for only a few examples. Thus, synthesis of tailor-made conjugated macromolecules such as end-functionalized polymers, block copolymers, star-shaped polymers is possible only in the case of substituted acetylenes. [Pg.18]

One of the major advantages of living free radical chemistry, when compared to other living procednres for the polymerization of vinyl monomers, is the stability of the initiating, or propagating, centers. This has enabled the development of a wide variety of functionalized unimolecular initiators for the synthesis of well-de ned linear polymers, block copolymers, and other complex macromolecnlar structures. ATRP of monomers with functionalized alkyl halide initiators leads... [Pg.607]


See other pages where Polymer block-copolymer is mentioned: [Pg.189]    [Pg.67]    [Pg.107]    [Pg.124]    [Pg.149]    [Pg.35]    [Pg.326]    [Pg.367]    [Pg.1121]    [Pg.106]    [Pg.1]    [Pg.1121]    [Pg.72]    [Pg.976]    [Pg.176]    [Pg.99]    [Pg.586]    [Pg.1154]    [Pg.240]    [Pg.775]    [Pg.76]    [Pg.292]    [Pg.206]    [Pg.1205]    [Pg.475]    [Pg.750]    [Pg.175]    [Pg.160]   
See also in sourсe #XX -- [ Pg.104 , Pg.105 , Pg.106 , Pg.107 , Pg.108 , Pg.109 ]

See also in sourсe #XX -- [ Pg.157 , Pg.159 ]




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