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Polycapro-lactone

Controlled block copolymerization of olefins with polar monomers was performed with a lanthanide complex by the successive polymerization of hexene (or pentene) and methylmethacrylate (or caprolactone). Polyhexene-block-poly(methyl methacrylate), polyhcxcnc-fo/ock-polycaprolactone, poly-pentene-fc/ock-poly(methyl methacrylate), and polypentene-Wock-polycapro-lactone were synthesized using a lanthanide complex as initiator [140-143]. [Pg.112]

The most direct way of looking at the specific interactions is by using spectroscopic measurements. Infra-red spectroscopy is the technique which has been most commonly used to study mixtures involving polymers. Studies of blends of PVC with polycaprolactone showed shifts of 4-6 cm in the carbonyl band of polycapro-lactone relative to the pure polymer but this Figure should be treated with... [Pg.157]

The most direct way of looking at the specific interactions is by using spectroscopic measurements. Infra-red spectroscopy is the technique which has been most commonly used to study mixtures involving polymers. Studies of blends of PVC with polycaprolactone showed shifts of 4-6 cm 1 in the carbonyl band of polycapro-lactone relative to the pure polymer 99 l00), but this Figure should be treated with caution as the peak probably consists of the sum of a shifted and an unshifted peak and it is difficult to say what the frequency of the shifted peak would be, or what fraction of the carbonyl groups are, or can be, involved in the interaction. Frequency shifts have also been shown to exist in blends of poly(methyl methacrylate) with poly(vinylidene fluoride)63). [Pg.157]

Most synthetic polymers are not biodegradable. However, there are a few synthetic polymers which are truly biodegradable. Some are water-soluble and become biodegradable once dissolved. Others are insoluble in water. The major families are lactic acid-based polymers, polycapro-lactone, other synthetic polyesters, and polyvinyl alcohol. [Pg.1074]

S4620 Poly- ester S8300 Poly- ether S4351 Polycapro- lactone 480A Not known 192A Not known 355D Not known 385 Not known J88 Not known PU 1478 Not known... [Pg.259]

PHB) [21] have a relatively large HSP distance and are experimentally found to be immiscible or at least only somewhat compatible. However [20], PBS can help the PLA to crystallize if a higher crystallinity version is desired. If it is not possible to find a good biopolymer match, HSP can be used to identify compatible polymers that are at least biodegradable. For example, the HSP match with polycapro-lactone is excellent and it is reported to be a useful polymer for blending with PLA [22]. [Pg.88]

Averous L., Moro L., Dole P, Fringant C. Properties of thermoplastic blends staich-polycapro-lactone, Po/> wer41 (2000)4157. [Pg.69]

Several studies are being conducted in order to improve PHBV mechanical properties and/or decrease its cost and enabling its industrial application. Among many studies it is possible to find addition of plasticizers (Choi and Park 2004), production of blends, including blends with natural polymers such as polycapro-lactone, poly(L-lactic acid), starch, and cellulose (El-Hadi et al. 2002 Ferreira et al. 2002) and also with synthetic polymers such as polyvynyl phenol (Fei et al. 2004), oxidized polyethylene, and polypropylene (Avella et al. 2002), blends with natural rubber (Han et al. 2004), among others. [Pg.84]

The N-cyanourea terminated resin synthesized from polycapro-lactone-diol, tolyene diisocyanate and cyanamide was applied on an aluminum plate about 3 mil of thickness, heated at 135 C for 10 minutes and stood at room temperature overnight. The cured film had an MEK rub over 100, and an excellent adhesion on aluminum. [Pg.104]

Because of their lesser ability to control shrinkage, the non-polar polymers such as polystyrene and polyethylene are often classified as low shrink rather than low profile additives. Usually, low profile additives are supplied as 30-40% polymer solutions in styrene monomer. Polyester resin manufacturers also package the low profile additives dissolved in their resins. These are referred to as one pack systems. As the industry has expanded, other thermoplastics have been identified which have shrinkage control properties. These are also now used commercially in a variety of applications. Examples of these other polyers are saturated polyesters, polyurethanes, stryene-butadiene copolymers and polycapro-lactones. Polyfvinyl acetate) based materials are probably still the most used low profile additives, being useful with the broadest range of unsaturated polyester resin structures. Relative proportions of the organics used in most formulations are 30-50% polyester alkyd, 10-20% thermoplastic and 40-50% styrene. [Pg.446]

A special polyester glycol type, polycapro-lactone glycol (XXVI), has become well established as a polyurethane adhesive component. And still another macroglycol type, poly butadiene glycol (Poly BD glycol) (XXVII) has gained use in polyurethane adhesive systems. [Pg.360]

Woodruff, M.A., Hutmacher, D.W., 2010. The return of a forgotten polymer—polycapro-lactone in the 21st century. Progress in Polymer Science 35 (10), 1217-1256. Available at http //linkinghub.elsevier.eom/retrieve/pii/S0079670010000419 (accessed... [Pg.28]

We will consider these groups one after the other and systematically try to understand the processes of crystallization as it concerns each group. To simplify these processes, we will consider first, the system of neat blends (i.e., without the deliberate addition of nanoparticles). The nanoparticles will be considered as one of the heterogeneities inside the blend. However, we should remember that the effect of the nanoparticles will depend greatly on the localization of the nanoparticles. In such ternary blends, preferential localization of the third component could be in either of the two polymers [21,22], which eventually affects the crystallization behavior. The preferential localization is driven by factors such as (i) thermodynamic (enthalpic interaction between each polymer and the third material) and/or (ii) kinetic factors (e.g., viscosity ratios of the two polymers) [36]. Wu et al. [22] reported the effect of localization of nanofillers, clay, and CNTs, on the morphology and crystallization of PLA/polycapro-lactone (PCL) blends. [Pg.291]

The 15N is a unique series of TPU grades based on polyether-polycapro-lactone copolymers offering excellent hydrolysis resistance in combination with good heat resistance and mechanical properties. Additionally, the 15N Series excels for its outstanding low temperature performance and elastic properties. [Pg.518]


See other pages where Polycapro-lactone is mentioned: [Pg.19]    [Pg.348]    [Pg.94]    [Pg.310]    [Pg.692]    [Pg.19]    [Pg.16]    [Pg.119]    [Pg.202]    [Pg.19]    [Pg.35]    [Pg.165]    [Pg.369]    [Pg.314]    [Pg.522]    [Pg.38]    [Pg.10]    [Pg.1057]    [Pg.153]    [Pg.624]    [Pg.139]    [Pg.2136]    [Pg.348]    [Pg.638]    [Pg.1387]   
See also in sourсe #XX -- [ Pg.119 ]




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