Abstract Four waterborne hyperbranched alkyd-acrylic resins (HBRAA) were synthesized by miniemulsion polymerization from a hyperbranched alkyd resin (HBR), methyl methacrylate (MMA), butyl acrylate (BA) and acrylic acid (AA), by using benzoyl peroxide (BPO) and ammonium persulfate (AP) as initiators. The reaction between HBR and acrylic monomers was evidenced by differential scanning calorimetric (DSC), nuclear magnetic resonance (NMR) and gel permeation chromatography (GPC). The conversion percentage, glass transition temperature (Tg), content of acrylic polymer (determined by soxhlet extraction) and molecular weight increased with the content of acrylic monomers used in the synthesis. The main structure formed during the synthesis was the HBRAA. The analysis by dynamic light scattering (DLS) showed that the particle size distribution of HBRAA2, HBRAA3 and HBRAA4 resins were mainly monomodal. The film properties (gloss, flexibility, adhesion and drying time) of the HBRAA were good.

Abstract A hyperbranched polyester polyol of the second generation (HBP2) was modified with polylactic acid (HBP2-g-PLA) and employed as a compatibilizer for plasticized tapioca starch (TPS)/polylactic acid (PLA) blends. The effect of the compatibilizer HBP2- g-PLA was evaluated in comparison to the control sample (TPS/PLA blend without HBP2-g-PLA). The torque value of the TPS/PLA blends with HBP2- g-PLA was lower than that of the control sample, while thermal stability and crystallinity followed opposite behavior. The glass transition temperature (Tg) and degree of crystallinity of the TPS/PLA blends with HBP2-g-PLA decreased with increasing mass fraction of HBP2-g-PLA. By scanning electron microscopy (SEM), it was observed that the morphology of the TPS/PLA blends with HBP2-g -PLA was more homogeneous than that of the control sample, confirming that HBP2- g-PLA acted as a compatibilizer and plasticizing agent to the TPS/PLA blends. Rheological analysis of the compatibilized TPS/PLA blends indicated the presence of microstructure.

Abstract New functional polymers will be prepared using alkyd resins having high solid content (environmentally friendly) and comb-type structural morphology. Different copolymers of hydroxyethyl acrylate and methyl methacrylate (HEMMA) were synthesized by solution polymerization using azo-bis-(isobutyronitrile) (AIBN) as initiator and dimethylformamide as a solvent. The proportions utilized of AIBN were 0.5 (HEMMA1), 1.0 (HEMMA2), 1.5 (HEMMA3) and 2.0 wt. % (HEMMA4). The conversion percentage of the reaction was higher than 90%. The formation of the copolymers was evidenced by infrared analysis, hydroxyl value, and nuclear magnetic resonance. The intensity of OH group adsorption increased with the molecular weight and hydroxyl value. The polydispersity index was lower than 1.5. All copolymers exhibited a stable region on viscosity at a shear rate between 0.1 and 10 s–1. The copolymers exhibited good thermal stability, flexibility, and adherence.

En este estudio, polietileno de baja densidad (PEBD) fue modificado con anhídrido maleico (AM) en estado fundido usando concentraciones diferentes de peróxido de dicumilo (DCP) (0.25, 0.50, 0.75 y 1.0 %). Los materiales obtenidos fueron caracterizados por contenido de gel, titulaciones ácido-base, análisis infrarrojo (IR), calorimetría de barrido diferencial (DSC), análisis termogravimétrico (TGA), análisis reológico, propiedades mecánicas, dureza y permeabilidad al oxígeno. El análisis reométrico indicó que el tiempo óptimo para obtener las mezclas es alrededor de 7.5 minutos. El análisis IR mostró que el AM fue injertado en el esqueleto del PEBD, el grado de injerto incrementó con el contenido de DCP y el más alto grado de injerto (1.12 ± 0.015 %), fue exhibido por la muestra obtenida empleando la mayor cantidad de DCP (1 %). La estabilidad térmica de las muestras funcionalizadas fue ligeramente mayor que la del PEBD. La cristalinidad de las muestras funcionalizadas fue diferente a la exhibida por el PEBD. El comportamiento reológico presentado por las muestras fue seudoplástico. Las propiedades mecánicas, dureza y la permeabilidad al oxigeno fueron dependientes de la cantidad de DCP y AM injertado en el PEBD.

Abstract In this work, low density polyethylene (LDPE)/plasticized starch (TPS) blends were prepared. The TPS employed in this study was obtained by plasticization of tapioca starch with a hyperbranched polyester polyol. Differential scanning calorimetry analysis showed that the melting temperature increased with the TPS content. The opposite effect was exhibited in the crystallization temperature and additional changes were not observed during the heating. X-ray diffraction analysis showed a reduction in intensity of the peak at Bragg’s angle 17.5°, proving a diminution on A type crystallinity with the increasing amount of LDPE. Micrographs obtained by scanning electron microscopy exhibited starch granules without destructure. TPS acted as a filler to LDPE, since the mechanical properties (Young’s modulus and tensile strength) improved ostensibly. The Young’ modulus and tensile strength decreased with the amount of LDPE, however, the elongation at break exhibited an opposite behavior.