Triblock copolymers structure

Structural Analysis of Hexagonal Mesoporous Silica Films Produced from Triblock-Copolymer-Structuring Sol-Gel... 

CHEMICAL NAME Linear styrene-butadiene-styrene triblock copolymer STRUCTURE [-CH-CH2-] ,-[-CH2-CH=CH-CH2-] -[-CH-CH2-] ... 

Block copolymers made from ethylene and propylene are valuable industrial materials. They can be used as thermoplastic elastomers and as compatibOizing agents for homopolymer blends. The properties of this type of copolymer depend on the microstructure of the blocks, the relative lengths of the blocks, and the overall molecular v eight. An ABA triblock copolymer structure containing crystalline A blocks and an amorphous B block can exhibit elastomeric behavior. The crystalline "hard" blocks can consist of isotactic or syndiotactic polypropylene (iPP or sPP) units or linear polyethylene (PE). The amorphous "soft" blocks can consist of atactic polypropylene (aPP) or ethylene-propylene copolymer (ethylene-propylene rubber, EPR). 

Thermodynamically stable, bicontinuous microemulsions have recently been shown to be obtainable in symmetric ternary blends of two homopolymers and a diblock copolymer by formulating alloys with compositions near mean-field isotropic Lifshitz points. In the present paper, it is argued that practical apphcation of this design criterion could require use of homopolymers of unequal molec.wts. and block copolymers of different structure. The existence of, and explicit location of, mean-field isotropic Lifshitz points in ternary blends with homopolymer molec.wt. asymmetry and either AB diblock or ABA triblock copolymer structures were demonstrated. These calculations significantly expanded the parameter space for observing bicontinuous miCToemulsions and allowed for more flexibility in tailoring melt rheological properties and solid-state mechanical properties. 29 refs. 

Novel polyimide-g-nylon 6 and nylon 6- polyiniide-] nylon 6 copolymers were synthesized by polycondensation and subsequent anionic, ring-opening polymerization methods. The graft and triblock copolymer structures were characterized with FTIR, GPC, selective extractions, DSC,TGA, tensile test and DMA. The effective reinforcement of nylon 6 with the incorporation of only a few wt% polyimide was demonstrated by the sigmOcant improvements in the copolymers thermal and mechanical properties, and chemical resistance. 

What are the two possible triblock copolymer structures of polybutadiene and cellulose ... 

Recently, the enhanced control of bulk and surface ordering of polypeptides has been employed to drive the processing and self-assembly of conductive rigid segments. Mainly triblock copolymer structures have been studied (see the following section). Manners and Winnik (Wang et al., 2008) synthesized a new type of metaUopolymer-polypeptide block copolymer poly(ferrocenyldimethylsilane)-fc-poly(8-benzyloxycarbonyl-L-lysine) (PFS-( -PZLLys) and studied their self-organization behavior in both the bulk state and in solution. In the bulk state, a cylindrical in-lamellar structure was observed in a compositionally asymmetric sample. Rod-like micelles with a polyferrocenylsilane core formed in a polypeptide selective solvent alone or in the presence of a common solvent. 

Mortensen K 1996 Structural studies of PEO-PPO-PEO triblock copolymers, their micellar aggregates and mesophases a small-angle neutron scattering study J. Phys. Condens Matters A103-A104... 

Figure 3.8. Schematic representation of the polystyrene domain structure in styrene-butadiene-styrene triblock copolymers. (After Holden, Bishop and Legge )...

At r = 0.5 (Fig. 9b), the most interesting and novel morphology can be observed. This morphology can be described as follows. The P4VP cores of the microspheres form a regular structure, and a P4VP bilayer surrounds each microsphere with a honeycomb-like structure, similar to a cell wall, as the number of the microsphere surrounded by the P4VP wall ( T) was 1.08. Similar structures have been observed for ABC triblock copolymers [39]. Our honeycomb-like novel structure, however, is different from that of the ABC triblock co-... 

Morphology of the anionically synthesized triblock copolymers of polyfp-methyl-styrene) and PDMS and their derivatives obtained by the selective chlorination of the hard segments were investigated by TEM 146). Samples with low PDMS content (12%) showed spherical domains of PDMS in a poly(p-methylstyrene) matrix. Samples with nearly equimolar composition showed a continuous lamellar morphology. In both cases the domain structure was very fine, indicating sharp interfaces. Domain sizes were estimated to be of the order of 50-300 A. 

Triblock copolymers of ABA type, where B is the central elastomeric block and A is the rigid end-block, are well-known commercially available polymers [7,8]. The chemical structures of some common TPEs based on styrenic block copolymers are given in Eigure 5.1. Synthesis of such ABA-type polymers can be achieved by three routes [9] ... 

This polypeptide is structurally identical to ABA-type triblock copolymer with a central hydrophdic elastomeric end-block capped with two hydrophobic plastic end-blocks and exhibits amphiphilic characteristics. The end-blocks of the polymer were chosen in such a way that their LCST would reside at or near room temperature. Thus the polymer exhibits phase separation, which is analogue to conventional TPEs, and offers TPE gels under physiological relevant conditions [104]. Glutamic acid residue is placed periodically in the elastomeric mid-block to increase its affinity towards the aqueous... 

Tailoring block copolymers with three or more distinct type of blocks creates more exciting possibilities of exquisite self-assembly. The possible combination of block sequence, composition, and block molecular weight provides an enormous space for the creation of new morphologies. In multiblock copolymer with selective solvents, the dramatic expansion of parameter space poses both experimental and theoretical challenges. However, there has been very limited systematic research on the phase behavior of triblock copolymers and triblock copolymer-containing selective solvents. In the future an important aspect in the fabrication of nanomaterials by bottom-up approach would be to understand, control, and manipulate the self-assembly of phase-segregated system and to know how the selective solvent present affects the phase behavior and structure offered by amphiphilic block copolymers. 

FIGURE 5 Stepwise synthesis of a triblock copolymer (PCL-PLA-PCL) of PCL and polylactic acid using aluminum coordination catalysts to minimize randomization of the block structure by transesterification. (From Ref. 43.)... 

The second case study. This involves all silica micro- and mesoporous SBA-15 materials. SBA-15 materials are prepared using triblock copolymers as structure-directing templates. Typically, calcined SBA-15 displays pore sizes between 50 and 90 A and specific surface areas of 600-700 m g with pore volumes of 0.8-1.2cm g h Application of the Fenton concept to mesoporous materials looks simpler since mass transfer would be much less limited. However, it is not straightforward because hydrolysis can take place in the aqueous phase. 

Drug Release from PHEMA-l-PIB Networks. Amphiphilic networks due to their distinct microphase separated hydrophobic-hydrophilic domain structure posses potential for biomedical applications. Similar microphase separated materials such as poly(HEMA- -styrene-6-HEMA), poly(HEMA-6-dimethylsiloxane- -HEMA), and poly(HEMA-6-butadiene- -HEMA) triblock copolymers have demonstrated better antithromogenic properties to any of the respective homopolymers (5-S). Amphiphilic networks are speculated to demonstrate better biocompatibility than either PIB or PHEMA because of their hydrophilic-hydrophobic microdomain structure. These unique structures may also be useful as swellable drug delivery matrices for both hydrophilic and lipophilic drugs due to their amphiphilic nature. Preliminary experiments with theophylline as a model for a water soluble drug were conducted to determine the release characteristics of the system. Experiments with lipophilic drugs are the subject of ongoing research. 

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). 

There has been considerable interest recently in an alternative type of ABA triblock structure, where the end blocks could form crystalline domains, by crystallization, rather than amorphous domains by phase separation. It was felt that, since such a crystallization process need not depend on the incompatibility between the blocks, it should be possible to have a homogeneous melt, which should exhibit a much lower viscosity, and hence much easier processing, than the heterogeneous media of the conventional triblock copolymers. Furthermore, thermoplastic... 

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