Centro UTN QUITEX - Difusión Científica - Artículos de Revista

Permanent URI for this collectionhttp://48.217.138.120/handle/20.500.12272/3851

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    Improving craft beer style classification through physicochemical determination and the application of deep learning techniques
    (2024-04-09) Gómez Pamies, Laura Cecilia; Bianchi, María Agostina; Farco, Andrea Paola; Vázquez, Raimundo Damián; Benítez, Elisa Inés
    The consumption of craft beer at fairs and festivals is a phenomenon that keeps growing in the world. For this reason, it is important to control the quality characteristics of the different styles. This study aimed to analyze the different styles of beer, classify them according to their physicochemical parameters, and propose a predictive pattern-based model known as deep learning that best defines the styles that are presented at festivals. Physicochemical analyses of final gravity, color, alcohol, bitterness, and α-acids were carried out on eight styles of beer. The first four parameters are those that characterize the styles according to the Beer Judge Certification Program style guide. The incorporation of the α-acid determination allowed a more realistic classification that considers the brewers’ new tendencies. This study will lay the foundations to improve local recipes, implement standardization, and provide training to local brewers
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    Impact of moisture and grinding on yield, physical, chemical and thermal properties of wholegrain flour obtained from hydrothermally treated sorghum grains
    (2020-02-03) Acquisgrana, María del Rosario; Gómez Pamies, Laura Cecilia; Martinez Amezaga, Nancy María Jimena; Quiroga, Fernanda Micaela; Ribotta, Pablo Daniel; Benítez, Elisa Inés
    The present work evaluates the potential of sorghum with high content of tannins for wholegrain flour production. Two types of mills were used: a roller mill (RM) and a blade (BM) mill. The impact of moisture and grinding on yield, physical, chemical and thermal properties were evaluated. Maximum yield was obtained using a BM with 25% moisture in the grain, resulting in 60.9% versus 28% (g flour g -1 wholegrain sorghum) for the RM. Grain moisture and milling type affected flour colour and ashes. For both mills, the pasting and thermal properties of flour with grain moisture variation were significantly different from the untreated control sample. By studying the procedures for flour production and quality characteristics, it is possible to produce flour with good physical attributes, which can contribute to the development of gluten-free foods based on sorghum for the coeliac population.
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    Augmentation of inductive effects through short range intramolecular hydrogen bonds for the improvement of cooperativity of trimeric rosettes
    (2024-02-26) Petelski, Andre Nicolai; Bundrea, Tamara; Peruchena, Nélida María
    Three key design elements improve the binding strength of trimeric rosettes: the direction of hydrogen bonds, the addition of groups with inductive effects, and the presence of ambifunctional intramolecular hydrogen bonds between the substituents.
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    Acidity of isomorphic substituted zeolites with B, Al and Ga revisited
    (2024-02-13) Petelski, Andre Nicolai; Peruchena, Nélida María; Zalazar, María Fernanda
    En este trabajo se analiza cómo afecta a a la acidez la sustitución de átomos de Silicio por átomos de Boro, Aluminio y Galio en tres tipos de zeolitas microporosas: BEA, FAU y MOR.
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    Nature and strength of weak O···O interactions in nitryl halide dimers
    (2022-12-14) Petelski, Andre Nicolai; Duarte, Darío Jorge Roberto; Peruchena, Nélida María
    The use of real space functions and molecular graphs has pushed some chemists to wonder: Are interactions between negatively charged oxygen atoms possible? In this contribution we analyze whether there is a real interaction between oxygen atoms in nitryl halide dimers (XNO2)2 (X=F, Cl, Br and I) and in tetranitromethane and derivatives. Based on ab-initio and density functional theories (DFT) methods, we show these complexes are weakly stabilized. Energy decomposition analy ses based on local molecular orbitals (LMOEDA) and interacting quantum atoms (IQA) reveal both dispersion and exchange play a crucial role in the stabilization of these complexes. Electron charge density and IQA analyses indicate that the oxygen atoms are connected by privileged exchange channels. In addition, electrostatic interactions between O and N atoms are also vital for the stabilization of the complexes. Finally, a reasonable explanation is given for the dynamic behavior of nitryl groups in tetranitromethane and derivatives.
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    Understanding the influence of alkali cations and halogen anions on the cooperativity of cyclic hydrogen-bonded rosettes in supramolecular stacks
    (2022-11-07) Petelski, Andre Nicolai; Fonseca Guerra, Célia
    Hydrogen-bonded supramolecular systems are known to obtain extra stabilization from the complexation with ions, like guanine quadruplex (GQ). They experience strong hydrogen bonds due to cooperative effects. To gain deeper understanding of the interplay between ions and hydrogen-bonding cooperativity, relativistic dispersion-cor rected density functional theory (DFT-D) computations were performed on triple layer hydrogen-bonded rosettes of ammeline interacting with alkali metal cations and halides. Our results show that when ions are placed between the stacks, the hydrogen bonds are weakened but, at the same time, the cooperativity is strengthened. This phenomenon can be traced back to the shrinkage of the cavity as the ions pull the monomers closer together and therefore the distance between the monomers becomes smaller. On one hand this results in a larger steric repulsion, but on the other hand, the donor-acceptor interactions are enhanced due to the larger overlap between the donating and accepting orbitals leading to more charge donation and therefore an enhanced electrostatic attraction.
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    Impact of covalent modifications on the hydrogen bond strengths in diaminotriazine supramolecules
    (2022-04-14) Petelski, Andre Nicolai; Pamies, Silvana Carina; Márquez, María Josefina; Peruchena, Nélida María; Sosa, Gladis Laura
    Melamine (M) is a popular triamine triazine compound in the field of supramolecular materials. In this work, we have computationally investigated how substituents can be exploited to improve the binding strength of M supramolecules. Two types of covalent modifications were studied: the substitution of an H atom within an amine group NHR, and the replacement of the whole NH2 group (R=H, F, CH3 and COCH3). Through our dispersion-corrected density functional theory computations, we explain which covalent modification will show the best self-assembling capabilities, and why the binding energy is enhanced. Our charge density and molecular orbital analyses indicate that the best substituents are those that generate a charge accumulation on the endocyclic N atom, providing an improvement of the electrostatic attraction. At the same time the substituent assists the main N H···N hydrogen bonds by interacting with the amino group of the other monomer. We also show how the selected group notably boosts the strength of hexameric rosettes. This research, therefore, provides molecular tools for the rational design of emerging materials based on uneven hydrogen-bonded arrangements.
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    How procyanidin C1 sticks to collagen : the role of proline rings
    (2021-05-29) Petelski, Andre Nicolai; Pamies, Silvana Carina; Sosa, Gladis Laura
    Molecular interactions between proteins and polyphenols are responsible for many natural phenomena like colloidal turbidity, astringency, denaturation of enzymes and leather tanning. Although these phenomena are well known, there are open questions about the specific interactions involved in the complexation process. In this work, Molecular Dynamic (MD) simulations and the topology of the electron density analysis were used to study the interactions between the flavonoid procyanidin C1 and a collagen fragment solvated in water. Root mean square deviation; root mean square fluctuation and hydrogen bonds occupancy were examined after 50 ns. The interactions were also analyzed by means of the quantum theory of atoms in molecules. Our results show that the main interactions are hydrogen bonds between –OH groups of the polyphenol and C––O groups of the peptide bond. Stacking interactions between proline rings and phenol rings, that is C–H⋯π hydrogen bonds, also stabilize the dynamic structure of the complex.
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    The impact of pirodextrin addition to improve physicochemical parameters of sorghum beer
    (2021-06-28) Goméz Pamies, Laura Cecilia; Lataza Rovaletti, María Mercedes; Martinez Amezaga, Nancy María Jimena; Benítez, Elisa Inés
    The traditional sorghum beer brewed by African communities differs from the traditional beer obtained from barley, mainly in the absence of hops and in a higher acidity level. People diagnosed with celiac disease find it as an alternative option when enjoying a good beer; however, some of the technological differences could be improved with the use of pyrodextrins obtained from the same cereal. In this work the use of pyrodextrins obtained by a treatment at 120 ◦C with acid during 360 min is proposed. A composite central design was made varying the concentration of pyrodextrins between 5 and 15 g/L and hop between 30 and 60 mg/L. The results indicate that the use of pyrodextrins up to a concentration of 10 g/L improves α-acid utilisation, bitterness and viscosity of the drink, achieving values similar to a typical lager beer obtained from barley. For 10 g/L pyrodextrin addition the increase in the wort and beer viscosity was 4.4% and 4.9%, respectively.
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    Understanding the chloride affinity of barbiturates for anion receptor design
    (2021-02-25) Petelski, Andre Nicolai; Márquez, María Josefina; Pamies, Silvana Carina; Sosa, Gladis Laura; Peruchena, Nélida María
    Due to their potential binding sites, barbituric acid (BA) and its derivatives have been used in metal coordination chemistry. Yet their abilities to recognize anions remain unexplored. In this work, we were able to identify four structural features of barbiturates that are responsible for a certain anion affinity. The set of coordination interactions can be finely tuned with covalent decorations at the methylene group. DFT-D computations at the BLYP-D3(BJ)/aug-cc-pVDZ level of theory show that the C—H bond is as effective as the N—H bond to coordinate chloride. An analysis of the electron charge density at the C—H···Cl— and N—H···Cl— bond critical points elucidates their similarities in covalent character. Our results reveal that the special acidity of the C—H bond shows up when the methylene group moves out of the ring plane and it is mainly governed by the orbital interaction energy. The amide and carboxyl groups are the best choices to coordinate the ion when they act together with the C—H bond. We finally show how can we use this information to rationally improve the recognition capability of a small cage-like complex that is able to coordinate NaCl.