3,800 research outputs found
Morphology and properties evolution upon ring-opening polymerization during extrusion of cyclic butylene terephthalate and graphene-related-materials into thermally conductive nanocomposites
In this work, the study of thermal conductivity before and after in-situ
ring-opening polymerization of cyclic butylene terephthalate into poly
(butylene terephthalate) in presence of graphene-related materials (GRM) is
addressed, to gain insight in the modification of nanocomposites morphology
upon polymerization. Five types of GRM were used: one type of graphite
nanoplatelets, two different grades of reduced graphene oxide (rGO) and the
same rGO grades after thermal annealing for 1 hour at 1700{\deg}C under vacuum
to reduce their defectiveness. Polymerization of CBT into pCBT, morphology and
nanoparticle organization were investigated by means of differential scanning
calorimetry, electron microscopy and rheology. Electrical and thermal
properties were investigated by means of volumetric resistivity and bulk
thermal conductivity measurement. In particular, the reduction of nanoflake
aspect ratio during ring-opening polymerization was found to have a detrimental
effect on both electrical and thermal conductivities in nanocomposites
Effect of morphology and defectiveness of graphene-related materials on the electrical and thermal conductivity of their polymer nanocomposites
In this work, electrically and thermally conductive poly (butylene
terephthalate) nanocomposites were prepared by in-situ ring-opening
polymerization of cyclic butylene terephthalate (CBT) in presence of a
tin-based catalyst. One type of graphite nanoplatelets (GNP) and two different
grades of reduced graphene oxide (rGO) were used. Furthermore, high temperature
annealing treatment under vacuum at 1700{\deg}C was carried out on both RGO to
reduce their defectiveness and study the correlation between the
electrical/thermal properties of the nanocomposites and the nanoflakes
structure/defectiveness. The morphology and quality of the nanomaterials were
investigated by means of electron microscopy, x-ray photoelectron spectroscopy,
thermogravimetry and Raman spectroscopy. Thermal, mechanical and electrical
properties of the nanocomposites were investigated by means of rheology,
dynamic mechanical thermal analysis, volumetric resistivity and thermal
conductivity measurements. Physical properties of nanocomposites were
correlated with the structure and defectiveness of nanoflakes, evidencing a
strong dependence of properties on nanoflakes structure and defectiveness. In
particular, a significant enhancement of both thermal and electrical
conductivities was demonstrated upon the reduction of nanoflakes defectiveness
Polyhedral oligomeric silsesquioxane (POSS) surface grafting: A novel method to enhance polylactide hydrolysis resistance
This work considers the development of an easy and scalable approach to change the features of poly(L-lactide) (PLLA) films, which is based on the application of a surface treatment with an amino-functionalized polyhedral oligomeric silsesquioxane (POSS). Indeed, the developed approach is based on the potential reactivity of POSS amino group towards the polymer functionalities to produce an aminolysis reaction, which should promote the direct grafting of the silsesquioxane molecules on the polymer surface. Neat and treated films were studied by infrared spectroscopy and X-ray photoelectron spectroscopy, which proved the effectiveness of POSS grafting. Moreover, scanning electron microscopy measurements demonstrated the homogeneous distribution of Si on the film surface treated with the silsesquioxane. The influence of the film treatment on the surface wettability was evidenced by contact angle measurements. These findings demonstrated a relevant enhancement of the surface hydrophobicity, which increase turned out to depend on the conditions applied, as it increased by increasing the reaction temperature and the contact time. Finally, in order to evaluate the stability of neat and of the treated PLLA films the surface morphology of the samples treated with pH 7.4 buffer at 50 \ub0C was studied
Efeito da aplicação do ferro dextrano sobre o desempenho de leitões lactentes produzidos no Sistema Intensivo de Suínos Criados ao Ar Livre - SISCAL.
bitstream/item/58544/1/CUsersPiazzonDocuments217.pd
Peso de leitoas de raça pura e mestiças do desmame aos cinco meses de idade.
bitstream/item/125544/1/COT149.pd
Unidade desenvolve tecnologia para manejo e bem-estar animal.
Projeto:11.11.11.111
Renewable and Tough Poly(l -lactic acid)/Polyurethane Blends Prepared by Dynamic Vulcanization
Melt blending of homopolymers is an effective way to achieve an attractive combination of polymer properties. Dynamic vulcanization of fatty-acid-based polyester polyol with glycerol and poly(l-lactic acid) (PLLA) in the presence of hexamethylene diisocyanate (HDI) was performed with the aim of toughening PLLA. The dynamic vulcanization in an internal mixer led to the formation of a PLLA/PU biobased blend. Melt torque, Fourier transform infrared (FTIR), and gel fraction analysis demonstrated the successful formation of cross-linked polyurethane (PU) inside the PLLA matrix. Scanning electron microscopy (SEM) analysis showed that the PLLA/PU blends exhibit a sea-island morphology. Gel fraction analysis revealed that a rubbery phase was formed inside the PLLA matrix, which was insoluble in chloroform. FTIR analysis of the insoluble part shows the appearance of an absorption band centered at 1758 cm-1, related to the crystalline carbonyl vibration of the PLLA component, thus suggesting the partial involvement of PLLA chains in the cross-linking reaction. The overall content of the PU phase in the blends significantly affected the mechanical properties, thermal stability, and crystallization behavior of the materials. The overall crystallization rate of PLLA was noticeably decreased by the incorporation of PU. At the same time, polarized light optical microscopy (PLOM) analysis revealed that the presence of the PU rubbery phase inside the PLLA matrix promoted PLLA nucleation. With the formation of the PU network, the impact strength showed a remarkable increase while Young's modulus correspondingly decreased. The blends showed slightly reduced thermal stability compared to the neat PLLA
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