ESPERIDIANA AUGUSTA BARRETOS DE MOURA

ESPERIDIANA AUGUSTA BARRETOS DE MOURA

(Fonte: Lattes)

Resumo

Graduated in Chemical Engineering at Faculdade Oswaldo Cruz (1983), Master in Nuclear Technology - Applications at IPEN / USP (1999), Ph.D. in Nuclear Technology - Applications at IPEN / USP (2006) and Post-Doctorate at Center for Advanced Materials ( T-CAM) from Tuskegee University, AL, USA. The main lines of research are: Synthesis of metallic nanoparticles; Obtaining and characterization of nanoparticles from mineral activity and agroindustry residues; Micro and nanofiller functionalization; Synthesis and reduction of graphene oxide; Development and modification of composite materials based on conventional and biodegradable polymers with vegetable fibers, micro and nanofillers of renewable origin; Development of biodegradable, active and intelligent plastic packaging for food, cosmetics, medical and pharmaceutical products; Development of conductive polymeric materials; Development of biomaterials for application in the regeneration of bone and dental tissue. (Text obtained from the Currículo Lattes on October 8th 2021)

Possui graduação em Engenharia Química pela Faculdade Oswaldo Cruz (1983), mestrado em Tecnologia Nuclear ? Aplicações pelo IPEN/USP (1999), doutorado em Tecnologia Nuclear ? Aplicações pelo IPEN/USP (2006) e Pós-Doutorado no Center for Advanced Materials (T-CAM) da Tuskegee University, AL, USA. As principais linhas de pesquisa são: Síntese de nanopartículas metálicas; Obtenção e caracterização de nanopartículas a partir de resíduos da atividade mineral e da agroindústria; Funcionalização de micro e nanocargas; Síntese e redução de óxido de grafeno; Desenvolvimento e modificaçao de materiais compósitos baseados em polímeros convencionais e biodegradáveis com fibras vegetais, micro e nanocargas de origem renovável; Desenvolvimento de embalagens plásticas biodegradáveis, ativas e inteligentes para alimentos, cosméticos, produtos médicos e farmacêuticos;Desenvolvimento de materiais poliméricos condutores; Desenvolvimento de biomateriais para aplicação na regeneração de tecidos ósseos e dentários. (Texto extraído do Currículo Lattes em 08 out. 2021)

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Effectiveness of modified lignin on poly(butylene adipateco-terephthalate)/poly(lactic acid) mulch film performance
2023 - BARROS, JANETTY J.P.; OLIVEIRA, RENE R.; LUNA, CARLOS B.B.; WELLEN, RENATE M.R.; MOURA, ESPERIDIANA A.B.
In this work, the biodegradable poly(butylene adipate-co-terephthalate) (PBAT)/ poly(lactic acid) (PLA) blend (ECOVIO®) and lignin, a renewable and biodegradable natural polymer with high UV absorption and modified by gamma radiation were used to produce agriculture mulch films. Lignin was gammairradiated at 30 and 60 kGy. The irradiated and non-irradiated lignin content of 2 wt% was incorporated into PBAT/PLA blend matrix using a twin-screw extruder and extrusion blown film to prepare flexible films. PBAT/PLA/LIGNIN films were characterized by Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC), x-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), tensile tests, contact angle, and UV–Vis analysis. FTIR spectra showed partial miscibility between PBAT/PLA and lignin, being intensified in irradiated lignin compounds. The DSC and XRD results confirmed that the degree of crystallinity of the blends was not significantly influenced by lignin addition. FE-SEM images showed better dispersion and miscibility in PBAT/PLA/Irradiated lignin. Miscibility improvement provided by irradiated lignin promoted better mechanical properties, mainly with lignin irradiated at 60 kGy. PBAT/PLA/LIGNIN films containing 2 wt% showed excellent UV-barrier property and greater hydrophobicity. Summing up, incorporation of low contents of irradiated lignin could be an interesting alternative to produce biodegradable UV-blocking agriculture mulch films.
Synergistic effect of e-beam irradiation and graphene oxide incorporation on thermal, mechanical, and barrier properties of poly (ethylene-co-vinyl alcohol) film
2022 - SANTANA, JULYANA G.; AKBULUT, MESHUDE; TEMPERINI, MARCIA L.A.; RANGARI, VIJAY K.; GUVEN, OLGUN; MOURA, ESPERIDIANA
Graphene and its derivatives, such as graphene oxide (GO), have attracted enormous interest from academia and industry because of its unique electrical, mechanical, and thermal properties, which can lead to enhanced material performance. In the present study, low contents of GO were incorporated into the poly (vinyl alcohol-co-ethylene) (EVOH). First, the GO was prepared by chemical oxidation of graphite employing a modified Hummer's method. The GO content of 0.1–0.3 wt % was incorporated in the EVOH matrix using a twin-screw extruder and extrusion blown film process to prepare flexible films. EVOH/GO film samples were irradiated at 100 kGy, using a 1.5 MeV electron-beam accelerator, at room temperature, in the presence of air. GO was characterized by XRD, ATR-FTIR, FE-SEM, and TEM analysis. XRD patterns of GO show a sharp reflection peak at 2θ = 10° (d001) corresponding to a d-spacing at 8.84 Å, characteristic of GO. The non-irradiated and irradiated samples were characterized by XRD, FEG-SEM, TG, DSC, oxygen transmission rate (OTR), UV/VIS analysis, and tensile tests. EVOH/GO nanocomposite films had an improved oxygen barrier, while also retaining fairly good transparency. As an effect of e-beam irradiation, the thermal, mechanical, and barrier behaviors of the nanocomposite films were even better than non-irradiated film samples, and obviously better than neat EVOH. Thus, the incorporation of low contents of GO followed by e-beam radiation treatment might be an interesting alternative to produce packaging materials based on EVOH with outstanding performance even under very humid conditions.
Enhanced miscibility of PBAT/PLA/lignin upon γ-irradiation and effects on the non-isothermal crystallization
2022 - BARROS, JANETTY J.P.; SOARES, CARLOS P.; MOURA, ESPERIDIANA A.B. de; WELLEN, RENATE M.R.
Lignin is natural and renewable polymer, the second most abundant on Earth. Properly used it can reduce synthetic and oil based materials in addition to contributing to the biodegradable systems. In this work, the kraft lignin was subjected to gamma radiation at absorbed doses of 30, 60, and 90 KGy in order to increase the interaction with “Poly(butylene adipate-co-terephthalate) (PBAT)/Poly(lactic acid) (PLA)” blend (Ecovio®). PBAT/PLA/lignin blends with 10% of the weight of lignin were produced by extrusion using twin-screw extruder and characterized by Fourier transform infrared spectroscopy (FTIR), Differential scanning calorimetry (DSC), and Field emission scanning electron microscopy (FE-SEM). FTIR spectra showed partial miscibility between PBAT/PLA and lignin, most due to the hydrogen bond between PBAT/PLA carbonyl and lignin hydroxyl, being intensified in irradiated lignin compounds. As evidenced on DSC scans, in PBAT/PLA/irradiated lignin the crystallization peak was shifted to lower temperatures and the crystallization rate decreased. Crystallization kinetics was modeled using Pseudo Avrami, and isoconversional models of Friedman and Vyazovkin. Pseudo-Avrami displayed linearity deviation at beginning and crystallization ending due to the nucleation and secondary crystallization, while from Friedman and Vyazovkin the activation energy (Ea) was higher for PBAT/PLA/irradiated lignin 30 KGy, characterizing crystallization with higher energy consumption. FE-SEM images showed better dispersion and miscibility in PBAT/PLA/irradiated lignin. The results indicate that the irradiation of Kraft lignin promotes miscibility and compatibility of PBAT/PLA/lignin.
Recycling expanded polystyrene with a biodegradable solvent to manufacture 3D printed prototypes and finishing materials for construction
2022 - BARTOLOMEI, SUELLEN S.; SILVA, FELIPE L.F. da; MOURA, ESPERIDIANA A.B. de; WIEBECK, HELIO
The amount of plastic waste generated is causing damage to the environment, such as sea and soil pollution, and one of the alternatives for disposing of polymers is recycling. This work proposes recycling expanded polystyrene using a biodegradable solvent, its plastification with glycerol, and the preparation of the composite with post-consumer recycled gypsum for applications to manufacturing by 3D printing and for finishing materials for construction. Specimen for tensile testing and shore D hardness were prepared by injection process and by 3D printing. In addition, Thermogravimetric (TG), Fourier-transform infrared spectrometry (FTIR), Differential scanning calorimeter, Scanning electron microscope (FESEM) analyses, and flame propagation tests were also carried out. TG and FTIR analyses show that the recycling process did not degrade the material, and the addition of glycerol and gypsum improved the thermal stability of the composite. The mechanical properties of the injected and 3D printed samples with gypsum were similar, due to the dimensional stability of the manufactured filament, which improved the speed and quality of the specimen printing. The increase in ductility and the reduction in the glass transition temperature showed that the recycled expanded polystyrene (RPS) were effectively plasticized with the addition of 2 wt% glycerol, preserving their flame self-extinguishment when subjected to the flame propagation test. Due to these properties, the plasticized RPS can be used to manufacture articles for finishing in civil construction, and the RPS composite can be used to manufacture 3D printed prototypes.
Lignin‑based polyethylene films with enhanced thermal, opacity and biodegradability properties for agricultural mulch applications
2021 - CHIAPPERO, LUCIO R.; BARTOLOMEI, SUELLEN S.; ESTENOZ, DIANA A.; MOURA, ESPERIDIANA A.B.; NICOLAU, VERONICA V.
Lignins are promising alternative raw materials for biocomposites due to their renewability, low cost and abundance. In this work, the use of (softwood and hardwood) Kraft lignins in the development of LLDPE/lignin films for agricultural mulch applications is studied. Processable blends were obtained from unmodified softwood lignin (SW) and from hardwood lignin modified by esterification (HWE). LLDPE was pelletized with (2.5%, 5% and 10%) lignin with particle size between 38 and 75 μm and flexible films were blown extruded. Processable extrusion blends showed temperature differences lower than 20 °C between the Tg of lignin and the melting temperature of LLPDE. Films from neat LLPDE and with 2.5% of HWE and up to 5% SW exhibited statistically comparable (≅ 349%) values of ductility. Ester groups present in lignin improve weight loss of lignin-based blends after soil buried test.
Mechanical and thermal properties of modified Georgian and Brazilian clay infused biobased epoxy nanocomposites
2021 - KODALI, DEEPA; UDDIN, MD-JAMAL; MOURA, ESPERIDIANA A.B.; RANGARI, VIJAK K.
This study focuses on the preparation and characterization of nanocomposite system with bio-based epoxy resin (Super SAP 100/1000, contains 37% bio-based carbon content) and natural clays including Georgian clay and Brazilian clay. Georgian clay was surface modified using an ultrasound processing in presence of Decalin. Brazilian clay was modified to organophilic bentonite using quaternary ammonium salts. The resulting nano clay particles were characterized using XRD and TEM to confirm the particle size reduction and uniform distribution. The as-fabricated nanocomposites were characterized using flexure, DMA, TMA and TGA. The flexure analysis showed that the modified clay composites have significant improvement in strength (23–38%) and modulus (28–37%). Delayed thermal degradation was observed from TGA analysis which showed that the major degradation temperatures improved from 7°-25°C. DMA and TMA analysis showed improvements in storage moduli (4–6%) and coefficient of thermal expansion (CTE) (6–64%), respectively. The notable improvement in thermal and mechanical properties suggested the effective dispersion and the high degree of polymer particle interaction. The bio based content present in the Super Sap 100/1000 acts as plasticizer resulting in the extensive ductility of the polymer.
Investigation of the effect of titanium dioxide and clay grafted with glycidyl methacrylate by gamma radiation on the properties of EVA flexible films
2020 - BARTOLOMEI, SUELLEN S.; SANTANA, JULYANA G.; DIAZ, FRANCISCO R.V.; KAVAKLI, PINAR A.; GUVEN, OLGUN; MOURA, ESPERIDIANA A.B.
Many studies report that nanocomposites obtained by dispersion of a small amount nanofiller into the polymer have remarkable improvements achieved in the mechanical and physical properties. However, in order to achieve this great improvement in properties, it is necessary that the nanofillers be dispersed homogeneously into the polymeric matrix. Often this dispersion is difficult to achieve due to the high interfacial energy of the nanoparticles present. This study reports the effect of gamma irradiation induced graft of glycidyl methacrylate (GMA) onto the surface of TiO2 and Clay nanofillers to improve their dispersion into the EVA matrix. The physical and mechanical properties of Ethylene-vinyl acetate copolymer (EVA) flexible films with these nanoparticles were studied. EVA nanocomposite with adding of the different amount of TiO2 and modified montmorillonite clay grafted and un-grafted with glycidyl methacrylate (GMA) using gamma irradiation have been prepared by melt extrusion. The nanocomposite flexible films were produced using a flat die extrusion process. The PGMA-grafted nanofillers were characterized by XRD and TEM analysis. The flexible films were characterized by Tensile tests, ATR–FTIR, UV–VIS, XRD, TG, and FE-SEM analysis to understand the nature of the interaction between the nanofillers and EVA matrix. The results showed that the addition of PGMA-grafted TiO2 and Clay nanofillers into EVA matrix improved the bonding between the nanofillers and matrix. It was also found that the PGMA-grafted nanofillers could be well dispersed into an EVA matrix in contrast to that of un-grafted. The tensile strength and modulus of the resulting EVA/TiO2-PGMA enhanced in comparison to that of un-grafted TiO2. The EVA/Clay-PGMA had slightly decreased tensile strength comparable to that of EVA/Clay but had considerably improved elastic modulus. In addition, the flexible films based on TiO2 exhibited high UV–Vis light absorption with energy gap shifted to the visible region. The results demonstrated that TiO2 and Clay nanofillers grafted with GMA by gamma radiation can be used to prepare EVA flexible films with improved bonding between the nanofillers and matrix and, consequently, enhanced properties for food and cosmetic packaging application.