Polyethylene block copolymers

Couman W.J., Heikens D., and Sjoerdsma S.D., Dilatometric investigation of deformation mechanism in polystyrene-polyethylene block copolymer blend Correlation between Poisson ratio and adhesion. 

LLDPE linear low density polyethylene block copolymer... 

PEG-PE poly(ethylene glycol)-polyethylene block copolymers... 

Figure 21 illustrates the separation of polystyrene-polyethylene blends at LCCC conditions. As can be seen, polyethylene elutes in the SEC mode whereas polystyrene elutes irrespective of its molar mass. The full separation of the blend components is accomplished within only 4 min. In addition to the separation of blends, the critical conditions for polystyrene were used for the separation of polystyrene/polyethylene block copolymers. 

To extend the use of polyethylene, it is desirable to enhance polyethylene s polarity, toughness, adhesion and compatibility with other materials. One approach is by incorporating polyethylene in block copolymer structures (Hong et al, 2002). Polyethylene block copolymers can maintain some of the superior properties of polyethylene while introducing the desired new properties from the other copolymer segments. In this way, the utility of polyethylene can be expanded to higher value areas, especially in polymer blends or composites, the preparation of micelles and the fabrication of nanoporous membranes (Wang and Hillmyer, 2001 Chen et al, 2009 Uehara et al, 2006 Uehara et al, 2009). 

The properties of polyethylene block copolymers depend on the structural and compositional parameters including the distribution and relative amounts of each segment, as well as... 

Polymethylene-1,3-cyclopentane) polyethylene block copolymer Microcrystal of PE Microcry stal/glassy state of pmcp... 

Polyethylene, block copolymer, random copolymer, blend compatibilizer, interfacial adhesion... 

Annis B K, Noid D W, Sumpter B G, Reffner J R and Wunderlich B 1992 Application of atomic force microscopy (AFM) to a block copolymer and an extended chain polyethylene Makromol. Chem., Rapid. Commun. 13 169 Annis B K, Schwark D W, Reffner J R, Thomas E L and Wunderlich B 1992 Determination of surface morphology of diblock copolymers of styrene and butadiene by atomic force microscopy Makromol. Chem. 193 2589... 

Similarly, the random introduction by copolymerization of stericaHy incompatible repeating unit B into chains of crystalline A reduces the crystalline melting point and degree of crystallinity. If is reduced to T, crystals cannot form. Isotactic polypropylene and linear polyethylene homopolymers are each highly crystalline plastics. However, a random 65% ethylene—35% propylene copolymer of the two, poly(ethylene- (9-prop5lene) is a completely amorphous ethylene—propylene mbber (EPR). On the other hand, block copolymers of the two, poly(ethylene- -prop5iene) of the same overall composition, are highly crystalline. X-ray studies of these materials reveal both the polyethylene lattice and the isotactic polypropylene lattice, as the different blocks crystallize in thek own lattices. 

By block copolymerisation so that one component of the block copolymer has a Tg well below the expected service temperature range (e.g polypropylene with small blocks of polyethylene or preferably polypropylene with small amorphous blocks of ethylene-propylene copolymer). 

Around Izod notch Low-density polyethylene Ethylene-propylene block copolymers Cellulose nitrate and propionate ABS and high-impact polystyrene Bis-phenol A polycarbonate... 

Whilst it is inevitable that polypropylene will be compared more frequently with polyethylene than with any other polymer its use as an injection moulding material also necessitates comparison with polystyrene and related products, cellulose acetate and cellulose acetate-butyrate, each of which has a similar rigidity. When comparisons are made it is also necessary to distinguish between conventional homopolymers and the block copolymers. A somewhat crude comparison between these different polymers is attempted in Table 11.7 but further details should be sought out from the appropriate chapters dealing with the other materials. 

The use of small amounts (0.5-3%) of polyethylene-polydimethylsiloxane or polystyrene-polydimethylsiloxane block copolymers in blends with a host... 

Compatibility and various other properties such as morphology, crystalline behavior, structure, mechanical properties of natural rubber-polyethylene blends were investigated by Qin et al. [39]. Polyethylene-b-polyiso-prene acts as a successful compatibilizer here. Mechanical properties of the blends were improved upon the addition of the block copolymer (Table 12). The copolymer locates at the interface, and, thus, reduces the interfacial tension that is reflected in the mechanical properties. As the amount of graft copolymer increases, tensile strength and elongation at break increase and reach a leveling off. 

RAFT polymerization has been used to prepare poly(ethylene oxide)-/ /wA-PS from commercially available hydroxy end-functional polyethylene oxide).4 5 449 Other block copolymers that have been prepared using similar strategies include poly(ethylene-co-butylene)-6/oci-poly(S-eo-MAH), jl poly(ethylene oxide)-block-poly(MMA),440 polyethylene oxide)-Moe -poly(N-vinyl formamide),651 poly(ethylene oxide)-Wot A-poly(NlPAM),651 polyfethylene ox de)-b ock-polyfl,1,2,2-tetrahydroperfluorodecyl acrylate),653 poly(lactic acid)-block-poly(MMA)440 and poly( actic acid)-6focA-poly(NIPAM),4 8-<>54... 

In a similar manner polyisoprene-polyethylene oxide block copolymers can prepared301. It is surprising that the poly(methyl methacrylate) anion can be successfully used for the polymerization of ethylene oxide without chain transfer302. Graft copolymers are also prepared by successive addition of ethylene oxide to the poly-... 

Multiblock polyethylene-polydimethylsiloxane copolymers were obtained by the reaction of silane terminated PDMS and hydroxyl terminated polyethylene oligomers in the presence of stannous octoate as the catalyst 254). The reactions were conducted in refluxing xylene for 24 hours. PDMS block size was kept constant at 3,200 g/mole, whereas polyethylene segment molecular weights were varied between 1,200 and 6,500 g/mole. Thermal analysis and dynamic mechanical studies of the copolymers showed the formation of two-phase structures with crystalline polyethylene segments. 

Short fiber reinforcement of TPEs has recently opened up a new era in the field of polymer technology. Vajrasthira et al. [22] studied the fiber-matrix interactions in short aramid fiber-reinforced thermoplastic polyurethane (TPU) composites. Campbell and Goettler [23] reported the reinforcement of TPE matrix by Santoweb fibers, whereas Akhtar et al. [24] reported the reinforcement of a TPE matrix by short silk fiber. The reinforcement of thermoplastic co-polyester and TPU by short aramid fiber was reported by Watson and Prances [25]. Roy and coworkers [26-28] studied the rheological, hysteresis, mechanical, and dynamic mechanical behavior of short carbon fiber-filled styrene-isoprene-styrene (SIS) block copolymers and TPEs derived from NR and high-density polyethylene (HOPE) blends. 

VandeVondele S, Voros J, Hubbell JA (2003) Rgd-grafted poly-l-lysine-graft- (polyethylene glycol) copolymers block non-specific protein adsorption while promoting cell adhesion. Biotechnol Bioeng 82 784—790... 

Under these conditions, the polyethylene oxide blocks behave chromatographi-cally invisible and retention of the block copolymer is solely directed by the polypropylene oxide block, yielding fractions of different degrees of polymerization (m) with respect to PPO. The assignment of the peaks was based on comparison with the chromatogram of a polypropylene glycol. 

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