Irene Teresinha Santos Garcia
Universidade Federal do Rio Grande do Sul
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Publication
Featured researches published by Irene Teresinha Santos Garcia.
Journal of Physical Chemistry B | 2011
Marcos A. Villetti; Clara Ismeria Damiani Bica; Irene Teresinha Santos Garcia; Fabiano V. Pereira; Francieli I. Ziembowicz; Carmen Luisa Kloster; Cristiano Giacomelli
Interactions between uncharged polymers and cationic surfactants are considered weaker than interactions with the anionic analogues. This work describes the binding occurring between methylcellulose (MC) and the cationic surfactant DTAB in aqueous medium. In the absence of salt, MC-DTAB exhibits a maximum in hydrodynamic radius, R(h,slow), with the increase in the surfactant concentration. Otherwise, in presence of salt the MC-DTAB system shows only a linear increase of R(h,slow). CAC is lower than the CMC, which is taken as an evidence of binding between the cationic surfactant and neutral polymer that induces the aggregation process. Static light scattering, rheology and micro-DSC results highlight the hydrophobic MC-DTAB association. Salt-out and the salt-in effects were observed in presence of DTAB, with a clear transition at concentration values close to the CMC, as judged from rheological and micro DSC measurements. Indeed, DTAB affects both the pattern of the sol-gel transition and the gel strength.
Polymer | 1998
Irene Teresinha Santos Garcia; Dimitrios Samios
Abstract High-density polyethylene (HDPE) and poly(vinylidene fluoride) (PVF2) were submitted to plane-straincompression at temperatures between the glass transition temperature (Tg) and the melting point (Tm) by using a deep channel die; this device allowed compression along the Z-axis, elongation along the X-axis and no dimensional change along the Y-axis. The thermomechanical and morphological changes occurring during the plastic deformation process and relaxation of the deformed materials were investigated by thermomechanical analysis, differential scanning calorimetry and density measurements. The results show that the deformation process affects the thermodynamic properties of polymers, introducing different characteristics into the material. An increase of amorphous phase was registered in both materials. The plastically deformed semicrystalline polymers showed non-regular linear thermal expansion behaviour in the deformation directions (X and Z). The relaxation process, which is obtained by heating the deformed materials, is characterized by ‘shape and temperature memory’.
Journal of the Brazilian Chemical Society | 2011
Michael Ramos Nunes; Giordana Martini Perez; Lara Fernandes Loguercio; Eliete Westphal Alves; Neftalí L. V. Carreño; Jorge Luiz Martins; Irene Teresinha Santos Garcia
Treads of scrap tires present low contents of inorganic fillers and a large amount of carbon black. In this work, this material was treated with potassium hydroxide and zinc chloride followed by pyrolysis at 500 and 700 °C. The ability to remove methylene blue and methyl orange were investigated under environmental conditions of pH and concentration. Carbons obtained with KOH at 700 °C present superior adsorption capacity. A simulation of this process permitted the characterization of the gases which contributed to surface development. The obtained products present a mesoporous structure and narrow particle size distribution. The presence of contaminants originated from these carbons was investigated in the aqueous media. The absence of zinc and sulfur releasing and the excellent ability to remove organic dye make these materials useful in the treatment of waste water.
Biomacromolecules | 2017
Patrick D. Mathews; Ana Carolina Monge Fernandes Patta; Joao Vitor Gonçalves; Gabriella S. Gama; Irene Teresinha Santos Garcia; Omar Mertins
Biomaterials conceived for vectorization of bioactives are currently considered for biomedical, biological, and environmental applications. We have produced a pH-sensitive biomaterial composed of natural source alginate and chitosan polysaccharides for application as a drug delivery system via oral administration. The composite particle preparation was in situ monitored by means of isothermal titration calorimetry. The strong interaction established between the macromolecules during particle assembly led to 0.60 alginate/chitosan effective binding sites with an intense exothermic effect and negative enthalpy variation on the order of a thousand kcal/mol. In the presence of model drugs mebendazole and ivermectin, with relatively small and large structures, respectively, mebendazole reduced the amount of chitosan monomers available to interact with alginate by 27%, which was not observed for ivermectin. Nevertheless, a state of intense negative Gibbs energy and large entropic decrease was achieved, providing evidence that formation of particles is thermodynamically driven and favored. Small-angle X-ray scattering provided further evidence of similar surface aspects independent of the presence of drug. The physical responses of the particles to pH variation comprise partial hydration, swelling, and the predominance of positive surface charge in strong acid medium, whereas ionization followed by deprotonation leads to compaction and charge reversal rather than new swelling in mild and slightly acidic mediums, respectively. In vivo performance was evaluated in the treatment of endoparasites in Corydoras fish. Systematically with a daily base oral administration, particles significantly reduced the infections over 15 days of treatment. The experiments provide evidence that utilizing particles granted and boosted the action of the antiparasitic drugs, leading to substantial reduction or elimination of infection. Hence, the pH-responsive particles represent a biomaterial with prominent characteristics that is promising for the development of targeted oral drug delivery.
Nuclear Instruments & Methods in Physics Research Section B-beam Interactions With Materials and Atoms | 2001
C.M. Lepienski; Irene Teresinha Santos Garcia; C.E. Foerster; F.C Serbena; F.C. Zawislak
Abstract The nanoindentation technique is used to measure hardness and Youngs modulus in 1.7 μm thick photoresist AZ-1350JTM films deposited on Si wafer and irradiated with He ions at 380 keV and at fluences of 1013, 1014 and 10 15 He cm −2 . After irradiation the films have been also submitted to isothermal treatments at 350°C for 6 h. The hardness value of 0.45 GPa for pristine film increases with ion irradiation to 2.3 GPa at the highest fluence. Thermal annealing, after irradiation, produces changes in the hardness behavior: for the lowest fluence the hardness raise from 0.7 to 1.0 GPa and for the highest fluence decreases from 2.3 to 1.8 GPa. The Youngs modulus values also follow a similar variation after irradiation and thermal treatment. These results are discussed in terms of the crosslinking and the carbonization produced by irradiation and thermal treatment.
Journal of Physical Chemistry B | 2017
Francieli I. Ziembowicz; Caroline R. Bender; Clarissa P. Frizzo; Marcos A. P. Martins; Thiane Deprá de Souza; Carmen Luisa Kloster; Irene Teresinha Santos Garcia; Marcos A. Villetti
Alkylimidazolium salts are an important class of ionic liquids (ILs) due to their self-assembly capacity when in solution and due to their potential applications in chemistry and materials science. Therefore, detailed knowledge of the physicochemical properties of this class of ILs and their mixtures with natural polymers is highly desired. This work describes the interactions between a homologous series of mono- (CnMIMBr) and dicationic imidazolium (Cn(MIM)2Br2) ILs with cellulose ethers in aqueous medium. The effects of the alkyl chain length (n = 10, 12, 14, and 16), type, and concentration range of ILs (below and above their cmc) on the binding to methylcellulose (MC) were evaluated. The thermodynamic parameters showed that the interactions are favored by the increase of the IL hydrocarbon chain length, and that the binding of monocationic ILs to MC is driven by entropy. The monocationic ILs bind more effectively on the methoxyl group of MC when compared to dicationic ILs, and this outcome may be rationalized by considering the structural difference between the conventional (CnMIMBr) and the bolaform (Cn(MIM)2Br2) surfactant ILs. The C16MIMBr interacts more strongly with hydroxypropylcellulose when compared to methylcellulose, indicating that the strength of the interaction also depends on the hydrophobicity of the cellulose ethers. Our findings highlight that several parameters should be taken into account when designing new complex formulations.
Journal of the Brazilian Chemical Society | 2018
Julia Cristina Oliveira Pazinato; Marcos A. Villetti; Omar Mertins; Emerson Rodrigo da Silva; Irene Teresinha Santos Garcia
Recent studies on tungsten oxide preparation are mainly motivated by its applications in smart windows, energy harvesting and, recently, in cancer therapy. Peroxotungstic acid (PTA) is an important precursor to obtain tungsten oxide in an environmentally-friendly way, through the colloidal synthesis in aqueous media. Despite giving chemically pure products, PTA originates oxides with various morphologies depending on the experimental conditions, a subject open to discussion. PTA, in the presence of sodium dodecyl sulfate (SDS) as architecture-directing agent, was investigated in ethanol/water medium by small angle X-ray scattering (SAXS), fluorescence, surface tension and conductivity measurements; the morphology of tungsten oxide obtained from the precursor systems was also characterized by scanning electron microscopy (SEM). PTA/SDS/ethanol/water systems show a two-level organization in which small micelles are aggregated as fractal structures. There is an inverse correlation between gyration radius of the fractal structures of the PTA/SDS systems and particle size of the tungsten oxide films. The interaction of PTA with SDS is observed by reducing the Gibbs energy of micellization; also, it is evidenced that the supressive effect of PTA on pyrene emission is overrided in presence of SDS.
Química Nova | 2013
Quelen Bulow Reiznautt; Bruna Girelli; Vinícius Millan Santa Catharina; Dimitrios Samios; Irene Teresinha Santos Garcia
On undergraduate courses, practical classes represent periods in which students can verify the concepts presented in theoretical classes. Conversely, the teaching internship in graduate programs allows these students to incorporate pedagogical practices into their experience, predominantly involving observation and reproduction of methods adopted by supervisors. We propose internship teaching as a period for reflection on our pedagogical practice and present a methodology for an experimental physical chemistry classroom. The students can interact with the experiment and instructor, furthering the study of ternary systems while developing their skills for investigative work.
Journal of Solid State Electrochemistry | 2012
Eliana Weber de Menezes; Michael Ramos Nunes; Leliz T. Arenas; Silvio L.P. Dias; Irene Teresinha Santos Garcia; Yoshitaka Gushikem; Tania Maria Haas Costa; Edilson Valmir Benvenutti
Materials Science and Engineering: C | 2009
Quelen Bulow Reiznautt; Irene Teresinha Santos Garcia; Dimitrios Samios
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Julia Cristina Oliveira Pazinato
Universidade Federal do Rio Grande do Sul
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