7 research outputs found
Thermal properties of amphiphilic biodegradable triblock copolymer of l,l-lactide and ethylene glycol
Preparation and characterization of poly(l,l-lactide)-b-poly(ethylene glycol)-b-poly(l,l-lactide) (PLLA-PEG-PLLA) microspheres having encapsulated tetracycline
Thermal and mechanical characterization of plasticized poly (L-lactide-co-D,L-lactide) films for food packaging
Controlling wettability of the each side of the PLA fabric through orientation of the working gases (O2 and CH4) during cold plasma treatment
This study aimed to obtain a bifunctional fabric from the point of view of hydrophilicity/hydrophobicity for biomedical applications. To achieve this, both sides of a fabric of polylactic acid (PLA) were subjected to a plasma treatment. While in a side the oxygen was introduced to the other side, simultaneously, was added methane. The plasma treatment was performed at 100 W, 1.8 mbar, during 30 minutes. By Scanning Electron Microscopy (SEM) morphological analysis, it became evident that the fabric side facing the oxygen inlet showed micropittings, while the reverse side had smooth surfaces. Analysis by X-Ray photoelectron spectroscopy (XPS) revealed an increase in the amount of oxygen in the surface of the PLA on both sides of the fabric. The surface function was characterized by measurements of water absorption rate, where it was determined that one fabric side was more hydrophilic than the other side. The results indicated achievement of a bifunctional fabric through orientation of working gases during a plasma treatment.The authors are acknowledging to financial support supplied by CAPES - BrasÃlia/Brazil through of the CAPES/IGC program - CGCI n° 055/2010
Evaluation of commercially available polylactic acid (PLA) filaments for 3D printing applications
Preparation of Polymeric Micelles of Poly(Ethylene Oxide-b-Lactic Acid) and their Encapsulation With Lavender Oil
Nanoparticles comprised of the poly(ethylene oxide)-b-poly (lactic acid) diblock copolymer (PEO-b-PLA) with and without the incorporation of lavender oil were prepared by nanoprecipitation. Diblock copolymers based on a fixed PEO block (5KDa) and two different PLA segments (4.5 or 10KDa) were used. The morphology, encapsulation efficiency, essential oil-polymer interaction and the release kinetics of the active agent in the nanoparticles, were evaluated. The hydrodynamic radius of the nanoparticles determined by light scattering was affected by the size of the poly(lactic acid) (PLA) block. The lavender essential oil encapsulation efficiency (at a concentration of 0.4 µL mL-1) determined by UV-VIS spectroscopy was in the range of 70-75%. The in vitro release suggests that the polymeric barrier is able to control the oil release
Geochemistry of the Serifos calc-alkaline granodiorite pluton, Greece: constraining the crust and mantle contributions to I-type granitoids
The Late Miocene (11.6–9.5 Ma) granitoid intrusion on the island of Serifos (Western Cyclades, Aegean Sea) is composed of syn- to post-tectonic granodiorite with quartz monzodiorite enclaves, cut by dacitic and aplitic dikes. The granitoid, a typical I-type metaluminous calcic amphibole-bearing calc-alkaline pluton, intruded the Cycladic Blueschists during thinning of the Aegean plate. Combining field, textural, geochemical and new Sr–Nd–O isotope data presented in this paper, we postulate that the Serifos intrusion is a single-zoned pluton. The central facies has initial 87Sr/86Sr = 0.70906 to 0.7106, εNd(t) = − 5.9 to −  7.5 and δ18Οqtz = + 10 to + 10.6‰, whereas the marginal zone (or border facies) has higher initial 87Sr/86Sr = 0.711 to 0.7112, lower ε Nd(t) = −  7.3 to − 8.3, and higher δ18Οqtz = + 10.6 to + 11.9‰. The small range in initial Sr and Nd isotopic values throughout the pluton is paired with a remarkable uniformity in trace element patterns, despite a large range in silica contents (58.8 to 72 wt% SiO2). Assimilation of a crustally derived partial melt into the mafic parental magma would progressively add incompatible trace elements and SiO2 to the evolving mafic starting liquid, but the opposite trend, of trace element depletion during magma evolution, is observed in the Serifos granodiorites. Thermodynamic modeling of whole-rock compositions during simple fractional crystallization (FC) or assimilation-fractional crystallization (AFC) processes of major rock-forming minerals—at a variety of pressure, oxidation state, and water activity conditions—fails to reproduce simultaneously the major element and trace element variations among the Serifos granitoids, implying a critical role for minor phases in controlling trace element fractionation. Both saturation of accessory phases such as allanite and titanite (at SiO2 ≥ 71 wt%)(to satisfy trace element constraints) and assimilation of partial melts from a metasedimentary component (to match isotopic data) must have accompanied fractional crystallization of the major phases