Search results for "Polyester"

Morphology, rheology, and mechanical properties of a new nanobiocomposite

2015

Nanobiocomposites are a new class of biodegradable polymer materials with an ultrafine phase dispersion of the order of a few nanometers in a biodegradable polymer matrix that shows very interesting properties often very different from those of conventional filled polymers. In this work the morphology and the rheological and mechanical properties of a new nanobiocomposite made of a biodegradable copolyester based blend with an organomodified montmorillonite have been investigated to evaluate its possible use in several applications. SAXS diffractograms and TEM micrographs show that the in both the adopted processing conditions an hybrid intercalated/exfoliated morphology is observed. Rheolo…

Effects of filler type and mixing method on the physical properties of a reinforced semirigid liquid crystal polymer

1996

Semirigid liquid crystalline polymers (LCPs) show some advantages with respect to rigid LCP: in particular lower processing temperatures, better compatibility with flexible thermoplastics, but also some disadvantages. Thermal resistance of rigid LCPs is much better and the maximum working temperature is, in general, very high. The thermomechanical properties can be improved by adding inorganic fillers. In this work processing, mechanical and thermomechanical properties of a filled semirigid liquid crystal copolyester are reported. Several inorganic fillers have been used in order to put in evidence the influence of shape and dimensions of the particles on the properties of the filled materi…

Rheological behavior of a semirigid liquid crystal polymer

1993

The rheological behavior of liquid crystal polymers is still far from completely clarified from both experimental and theoretical points of view. In this paper, the shear flow and the non-isothermal elongation flow behavior of a semi-rigid liquid crystal copolyester is discussed. The viscosity strongly decreases when the test temperature is increased above the crystal-nematic transition temperature; below this temperature the viscosity is very high. The thermal history strongly affects the shear viscosity. The elongational flow behavior depends also on temperature. Above the crystal-nematic transition temperature and the mesophase is easily spinnable, whereas below this temperature, the spi…

THERMOTROPIC HOMOPOLYESTERS. IV. STUDY OF FIBER FORMATION.

1983

We report a melt spinning and viscosity study of two semiflexible homopolyesters containing both rigid and flexible segments in the repeating unit. Single filaments of the polyesters formed from 4,4′-diacetoxybiphenyl and azelaic acid (PB7) and sebacic acid (PB8), and from 4′-hydroxyphenyl-4-hydroxycinnamate and azelaic acid (C7), were spun at temperatures between 205 and 255°C. The temperature dependence of the Newtonian melt viscosity of PB7 and C7 was investigated, and a range of molecular weights was studied for PB7. The spinning parameters, fiber characteristics, and viscosity-temperature behavior are related to the type of mesophase formed. The mechanical properties of fibers spun fro…

Biopolymer based nanocomposites reinforced with graphene nanoplatelets

2016

In this work, biopolymer based nanocomposites filled with graphene nanoplatelets (GnP) were prepared by melt compounding in a batch mixer. The polymer used as matrix was a commercial biodegradable polymer-blend of PLA and a copolyester (BioFlex®). The prepared materials were characterized by scanning electron microscopy (SEM), rheological and mechanical measurements. Moreover, the effect of the GnP amount on the investigated properties was evaluated. The results indicated that the incorporation of GnP increased the stiffness of the biopolymeric matrix.

Thermomechanical degradation of PLA-based nanobiocomposite

2015

Nanobiocomposites are a new class of biodegradable polymer materials with nanometric dispersion of inert particles in a biodegradable polymer matrix that show very interesting properties often very different from those of conventional- filled polymers and also biodegradability. An important issue in the applications of the biodegradable polymers is their easy degradability during processing due to the thermomechanical stress or to the presence of humidity. In this work, the thermomechanical degradation behavior of a nanobiocomposite made by a PLA-based blend and an organomodified montmorillonite has been investigated. The degradation kinetics has been followed by means of rheological, mecha…

Functionalization of aliphatic polyesters by nitroxide radical coupling

2014

Functionalized poly(butylene succinate) (PBS) samples were prepared by a post-polymerization method based on the coupling reaction between TEMPO derivatives bearing different functionalities and PBS macroradicals generated by H-abstraction using a peroxide. 4-Benzoyloxy-2,2,6,6-tetramethylpiperidine-1- oxyl (BzO-TEMPO) and 4-(1-naphthoate)-2,2,6,6-tetramethylpiperidine-1-oxyl (NfO-TEMPO), a pro-fluorescent nitroxide, were successfully grafted on PBS, as revealed by MALDI TOF MS and UV-Vis spectroscopy. The functionalization degrees were accurately determined by UV-Vis analysis and confirmed by 1H-NMR spectroscopy. The grafting site was identified by combining theoretical calculations with e…

On the compatibilization of PET/HDPE blends through a new class of copolyesters

2000

Polyethyleneterephthalate (PET) and polyethylene are incompatible polymers and their blends show, in general, poor properties. Compatibilization is then a necessary step to obtain blends with good mechanical and barrier properties. In this work different compatibilizing agents were used, i.e. a maleic anhydride elastomer and some new products containing graft-copolymers having polyester segments grafted onto polyethylene backbone chains. Both the functionalized elastomer and the new products drastically improve the morphology and the ductility of the blend. In the case of the modified elastomer the compatibilizing action has been attributed to the formation of H-bonds whereas the copolymers…

One-pot synthesis of poly(l-lactide) multi-arm star copolymers based on a polyester polyol macroinitiator

2013

Abstract Using a hyperbranched poly(glycolide) ( hb PGA) macroinitiator the synthesis of poly( l -lactide) (PLLA) multi-arm star polyesters has been achieved via a core-first approach. The star-shaped copolymers were prepared in a one-pot two-step process via Sn(Oct) 2 -catalyzed ring-opening polymerization (ROP) conducted in the melt. Complete conversion of the end groups of the hb polyglycolide polyester polyols is ensured by the reactive primary hydroxyl termini. By adjusting the monomer/initiator ratio a series of star copolymers with varying PLLA arm length has been obtained with molecular weights in the range of 1500 to 10,000 g/mol (SEC). The successful coupling of the PLLA arms to t…

1989

A series of combined main-chain side-group liquid-crystalline polymers was synthesized by melt polycondensation from trans-1,4-cyclohexanedicarboxylic acid, chloro-1,4-phenylene diacetate and 6-(4-methoxy-4′-biphenylyloxy)hexyl-1,4-phenylene diacetate. These polyesters combine the features of rigid-rod main-chain LC-polymers and of side-group LC-polymers. Polymers with small fractions of mesogenic side-groups (5 and 10 mol-%) have lower melting points than the parent polymer poly(chloro-1,4-phenylene 1,4-cyclohexanedicarboxylate) but are still liquid crystalline up to their decomposition at T ≥ 400°C. In polymers with larger fractions of mesogenic side-groups (50 and 100 mol-%) partial isom…