This study describes the chemical composition and biological activities of extracts and compounds obtained from the roots of Bowdichia virgilioides (Fabaceae). A mixture of very long-chain free fatty acids (VLFAs) and pure compounds, namely isocordoin, cordoin, lupeol, lupenone, β-sitosterol, stigmasterol, and sitostenone, were isolated from the soluble fraction of the methanol extract by using sequential column chromatography procedures. The molecular structures of the compounds were determined using infrared (IR), nuclear magnetic resonance (NMR), and mass spectrometry (MS) techniques. Notably, this is the first report of the occurrence of both chalcones within this plant genus. Besides, the VLFAs were identified by electrospray ionization mass spectrometry (ESIMS) and the presence of these compounds in roots is suggested to be an adaptive response to environmental stress, which exhibited moderate antioxidant properties when tested against the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical and in the β-carotene/linolenic acid auto-oxidation assay. However, the MeOH soluble fraction demonstrated significant toxicity in the brine shrimp lethality assay. Fabaceae. Fabaceae . (Fabaceae) longchain long chain (VLFAs isocordoin cordoin lupeol lupenone βsitosterol, βsitosterol β sitosterol, sitosterol β-sitosterol stigmasterol sitostenone procedures IR, IR , (IR) NMR, NMR (NMR) MS (MS techniques Notably genus Besides ESIMS (ESIMS stress 2,2diphenyl1picrylhydrazyl 22diphenyl1picrylhydrazyl diphenylpicrylhydrazyl 2,2 diphenyl 1 picrylhydrazyl 2 DPPH (DPPH βcarotene/linolenic βcarotenelinolenic carotene/linolenic carotene linolenic autooxidation auto oxidation assay However (Fabaceae (IR (NMR 2diphenyl1picrylhydrazyl 22 2, βcarotene carotenelinolenic

Parthenolide (PTN) is a secondary metabolite of the plant Tanacetum parthenium (L.) Schulz Bip. and is considered the chemical marker of this species. This sesquiterpene lactone (germacrene skeleton) has been described as responsible for the biological activity of the leaf extract. In addition, several studies in the literature have demonstrated its antiparasitic and antineoplastic activity. However, there is a need for knowledge of other safety parameters, such as pharmacokinetic, pharmacodynamic and toxicity evaluations. Therefore, in this investigation, the in vitro metabolism of parthenolide was performed with rat liver microsomes and biomimetic metabolism (such as cytochrome P-450 system) using organometallic catalysts. The biomimetic procedure was validated since the major compound of biomimetic oxidative reaction with meta-chloroperbenzoic acid catalyzed by metalloporphyrin 5,10,15,20-tetrakis(pentafluorophenyl)-porphyrin iron(III) chloride was also observed with rat liver microsomes. Previous chemoenzymatic synthesis studies of PTN afforded the same epoxide formation, this major oxidative compound was isolated and fully characterized as (1 R,10R)-epoxyparthenolide based on experimental and theoretical calculations of infrared (IR) and vibrational circular dichroism (VCD) data at the B3PW91/6-311G. Furthermore, for the first time, this metabolite was evaluated for trypanocidal and leishmanicidal activity. The mean inhibitory concentration (IC50) values were lower for PTN than its metabolite and showed significant cytotoxic effects for both parasites. This finding holds promise for addressing neglected diseases. (PTN L. L (L. Bip species germacrene skeleton extract addition However parameters pharmacokinetic evaluations Therefore investigation P450 P 450 P-45 system catalysts metachloroperbenzoic meta chloroperbenzoic 5,10,15,20tetrakispentafluorophenylporphyrin 5101520tetrakispentafluorophenylporphyrin tetrakispentafluorophenylporphyrin 5,10,15,20 tetrakis pentafluorophenyl porphyrin 5 10 15 20 ironIII iron III iron(III formation 1 ( R,10Repoxyparthenolide R10Repoxyparthenolide RRepoxyparthenolide R,10R epoxyparthenolide R 10R IR (IR VCD (VCD B3PW91/6311G. B3PW916311G BPWG B3PW91/6 311G. B3PW91 6 311G B PW G B3PW91/6-311G Furthermore time IC50 IC (IC50 parasites diseases (L P45 45 P-4 20tetrakispentafluorophenylporphyrin 5101520 5,10,15,2 2 10Repoxyparthenolide Repoxyparthenolide R10R RR 6311G B3PW91/6311G B3PW916 BPW B3PW91/ B3PW9 IC5 (IC5 P4 4 P- 510152 5,10,15, B3PW (IC 51015 5,10,15 5101 5,10,1 510 5,10, 51 5,10 5,1 5,

Bisphenol A (BPA), an endocrine disruptor used in different commercial polymers, is a persistent pollutant commonly found in effluents. Conventional wastewater treatment processes have low chemical removal efficiency and are expensive. This work evaluated BPA removal using laccase enzyme produced from white rot fungus Pleurotus ostreatus. For the enzymatic production, residues of acai berry and pineapple were used as laccase inducers. The use of natural inducers led to a high enzyme production (1139 and 1031 U mL−1 to acai and pineapple, respectively). Bisphenol A was removed to a concentration lower than LOD (limit of detection) after 4 h. The degradation mechanism of BPA occurred by oxidation of methyl to hydroxymethyl group in a propane portion, with breakdown of the aromatic ring. The developed technology brought to the scene a new green, viable methodology, using vegetable waste, adding value to these residues and bringing an alternative to the BPA treatment. BPA, , (BPA) polymers effluents expensive ostreatus 1139 (113 103 mL1 mL 1 mL− respectively. respectively . respectively) limit detection h portion ring green methodology waste (BPA 113 (11 10 11 (1 (

Schiff bases are diverse organic compounds with an azomethine structure (–C=N–), holding potential in both chemistry and biology. They serve as catalysts, stabilizers, and exhibit various biological activities. The molecular structure of Schiff bases influences their biological properties, including antimicrobial effects. Redox-active compounds with more negative potentials tend to be more effective against microbes. In one of our recent studies, we explored the antimicrobial properties of two Schiff bases derivatives, SB-1 ((E)-4-amino-3-((3,5-di-tert-butyl-2-hydroxybenzylidene)amino) and SB-2 ((E)-2-((4-nitrobenzilidene)amino)aniline). SB-1 showed antibacterial activity against certain Gram-positive bacteria, while SB-2 did not. The difference in their cyclic voltametric profiles, especially SB-1’s more negative reduction potential, prompted us to carry out further characterizations, including scan-rate studies, solvent analysis, and computational calculations. We found that SB-1, which presents a stable intramolecular hydrogen bond, undergoes irreversible oxidation, likely at the –NH2 group, and a quasi-reversible reduction via an intramolecular reductive coupling of the (–C=N–) azomethine group, supported by orbital theoretical calculations. This research sheds light on the potential applications of Schiff bases in antimicrobial contexts, guided by their redox properties and structure. –C=N–, CN –C=N– , C N biology catalysts stabilizers activities effects Redoxactive Redox active microbes studies derivatives SB1 SB 1 SB- E4amino33,5ditertbutyl2hydroxybenzylideneamino E4amino335ditertbutyl2hydroxybenzylideneamino Eaminoditertbutylhydroxybenzylideneamino E 4 amino 3 3,5 di tert butyl 2 hydroxybenzylidene 5 ((E)-4-amino-3-((3,5-di-tert-butyl-2-hydroxybenzylidene)amino SB2 E24nitrobenzilideneaminoaniline. E24nitrobenzilideneaminoaniline Enitrobenzilideneaminoaniline nitrobenzilidene aniline . ((E)-2-((4-nitrobenzilidene)amino)aniline) Grampositive Gram positive bacteria not profiles SB1s SBs s characterizations scanrate scan rate analysis calculations SB1, 1, bond oxidation NH2 NH –NH group quasireversible quasi reversible (–C=N– contexts –C=N E4amino33 5ditertbutyl2hydroxybenzylideneamino ditertbutyl hydroxybenzylideneamino 35 3, nitrobenzilideneaminoaniline ((E)-2-((4-nitrobenzilidene)amino)aniline (–C=N Eamino E4amino3 ditertbutylhydroxybenzylideneamino E4amino

In this work, using the PM3 semi-empirical method, the oxidation of the single-walled carbon nanotube (SWCNT) was studied by sulfuric and nitric acid for the incorporation of carbonyl (C=O), phenol (OH) and carboxylic (COOH) groups in the C=C bonds present on the surface of the nanotube. Subsequently, the crosslinking of the oxidized SWCNT (SWCNTox) and chitosan (Q) was observed through hydrogen bonds of the C=O and OH bonds with 2.34 Å, the process was endothermic and soluble in polar solvents due to the presence of OH and NH groups in the structure of SWCNTox/Q. The Monte Carlo modeling allowed to study the adsorption of pesticides in the SWCNTox/Q at different temperatures, where the QSAR (quantitative structure activity relationship) properties allowed predicting the behavior of the pesticides, that is, the degree of hydrophobicity (log P) and accessible surface area (ASA) were important parameters in the evaluation of SWCNTox/Q as an adsorbent and surface interacting with pesticides respectively. Finally, the adsorption was a physisorption process due to the electronegativity of the CO, OH, NH2, NH and C=O bonds. work PM semiempirical semi empirical method singlewalled single walled (SWCNT C=O, CO , C O (C=O) (OH COOH (COOH CC Subsequently SWCNTox (SWCNTox Q (Q 234 2 34 2.3 Å SWCNToxQ temperatures quantitative relationship is log P ASA (ASA respectively Finally NH2 (C=O 23 3 2.

Nanoparticles of TiO2 doped with low amount of Fe were synthesized from natural ilmenite obtained from alluvial gold mine wastes. The obtained TiO2 were characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), Fourier-transform infrared spectroscopy (FTIR), UV-Vis diffuse reflectance, thermogravimetric analysis/differential scanning calorimetry (TGA/DSC), N2 adsorption-desorption isotherms, transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The results confirm the formation of mesoporous TiO2 nanoparticles in anatase phase with 0.05 wt.% of iron possibly replacing some titanium places. All the characterizations were performed to the synthesized solid and the reference materials (TiO2 anatase and Degussa P25). The photocatalytic activity of both the synthesized solid and references were evaluated in the photo-oxidation of cyanide in aqueous medium under UV illumination. An experimental design type Box-Behnken was performed choosing three different parameters: the initial concentration of cyanide (50, 150 and 250 ppm) the catalyst load (0.1, 0.5 and 1.0 g L-1) and the oxygen source. The percentage of cyanide conversion was chosen as response in the design obtaining as optimal conditions [CN-]0 = 50 ppm, catalyst load = 0.6 g L-1 and air bubbling. Under these conditions it was reached 32, 32 and 89% of cyanide conversion for Fe-TiO2 synthesized, TiO2 anatase and Degussa P25, respectively. TiO wastes Xray X ray XRD, XRD , (XRD) XRF, XRF (XRF) Fouriertransform Fourier transform FTIR, FTIR (FTIR) UVVis Vis reflectance analysisdifferential analysis differential TGA/DSC, TGADSC TGA/DSC TGA DSC (TGA/DSC) N adsorptiondesorption adsorption desorption isotherms TEM (TEM XPS. XPS . (XPS) 005 0 05 0.0 wt wt. places (TiO P25. P25 P P25) photooxidation photo oxidation illumination BoxBehnken Box Behnken parameters 50, (50 15 25 ppm 0.1, 01 1 (0.1 5 0. 10 1. L1 L source CN0 CN [CN-] 06 6 L- bubbling 3 89 FeTiO2 FeTiO Fe-TiO respectively (XRD (XRF (FTIR (TGA/DSC (XPS 00 P2 (5 2 0.1 (0. [CN- 8 ( (0 [CN

Bulk precipitation (BP) samples were collected at two coastal urban sites and two montane Atlantic Forest (400 and 1000 m altitude) areas in southeastern Brazil from August 2008 to August 2009. These samples were analyzed for the major inorganic ions (H+, Na+, K+, Ca2+, Mg2+, Cl- and SO42-) found in rainwater. The concentrations of inorganic nitrogen species (NH4+, NO3- and NO2-) were compiled from a previous study. The volume-weighted mean (VWM) concentrations of inorganic ions differed spatially, with higher values at the coastal urban and coastal periurban sites. On a molar basis, Cl- and Na+ together comprised 60% of the total inorganic constituents at the coastal urban site and 34-42% at the other three sites, as it is the closest to the ocean. Magnesium was also primarily associated with sea-salt aerosol. Non-sea-salt (nss) fractions of K+, Ca2+ and SO42- comprised 68-93% of their VWM concentrations, indicating the contribution of natural (mostly biogenic) and anthropogenic (SO2 oxidation for the latter) sources. Finally, we found that the acidity of BP at the four sampling sites is primarily controlled by the NH4+, nss-Ca2+, nss-SO42-, and NO3- ions, resulting in VWM pH values ranging from 5.60 (lower montane forest) to 5.98 (coastal periurban site). (BP 400 (40 100 altitude 200 2009 H+, H (H+ Na K K+ Ca2 Ca Mg2 Mg Mg2+ Cl SO42 SO rainwater NH4 NH (NH4+ NO3 NO NO2 NO2- study volumeweighted volume weighted (VWM spatially basis 60 3442% 3442 34 42% 42 34-42 ocean seasalt sea salt aerosol Nonseasalt Non nss (nss 6893% 6893 68 93% 93 68-93 mostly biogenic SO2 (SO latter sources Finally NH4+ nssCa2+, nssCa2 nssCa nss-Ca2+ nssSO42, nssSO42 nssSO , nss-SO42- 560 5 5.6 lower forest 598 98 5.9 site. . site) 40 (4 10 20 H+ (H SO4 (NH4 6 344 3 4 34-4 689 9 68-9 nssCa2+ nss-Ca2 nssSO4 nss-SO42 56 5. 59 ( 1 2 (NH 34- 68- nss-Ca nss-SO4 nss-SO

The aim of this study was to effectively remove Fe2+ by using ozone microbubbles in bottled mineral water to prevent sediment from occurring during storage and increase shelf life. By considering the characteristics of mineral water with low solubility of ozone and high CO2 content, a suitable ozone injection step was chosen and a new mineral water treatment method using microbubbles was proposed. As a result of the treatment of the bottled mineral water with ozone microbubbles, the concentration of the iron ion was reduced from 0.14 to 0.01 mg L-1, and the shelf life increased to 360 days. During the treatment, the concentrations of K+ and Na+ were almost unchanged, and the deposition time was reduced to one-third compared to the natural oxidation. Fe2 Fe CO content proposed 014 0 14 0.1 001 01 0.0 L1, L1 L 1, 1 L-1 36 days K Na unchanged onethird one third oxidation 0. 00 L- 3

Summary: The castor plant (Ricinus communis L.) is a plant that has dif ferent benefits, such as the production of biodiesel and soil bioremediation. Due to the above, the castor plant’s ability to extract arsenic (As) was evaluated. For this, a randomized block experimental design with four repetitions was carried out. The evaluated treatments consisted of two types of biosolids (oxidation lagoon biosolids (BLO) and activated sludge biosolids (BLA) and four doses of As (0, 25, 50, 100 mg kg-1), under greenhouse conditions. As concentration was determined by inductively coupled plasma mass spectrometry (ICP-MS). From the quantification of As, the translocation factor (TF) and the bioaccumulation factor (FB) were estimated. The total nitrogen (N) content was quantified by the combustion method. Phosphorus (P) was analyzed by colorimetry using the metavanadate method, and the content of potassium (K), calcium (Ca), magnesium (Mg), copper (Cu), manganese (Mn), iron (Fe) and zinc (Zn) was quantified by atomic absorption. For percentage of oil The Soxhlet method was used in the seed. The plant height and the dry weight of biomass did not vary due to the treatment ef fect (P ≤ 0.05). The Translocation Factor (TF) and the Bioconcentration Factor (BCF) registered ranges of 0.20 - 0.63 and 0.28 - 0.75, respectively. The applied doses of As did not af fect the biomass and nutrient absorption in the castor plant, which indicates that this plant species is tolerant to toxicity with productive potential in soils contaminated with this element, in concentrations up to 100 mg kg-1.

Resumen: La higuerilla (Ricinus communis L.) es una planta que tiene diferentes beneficios, como la producción de biodiesel y la biorremediación de suelo. Debido a lo anterior, se evaluó la capacidad de la higuerilla para extraer arsénico (As). Para ello, se realizó un diseño experimental de bloques al azar con cuatro repeticiones. Los tratamientos evaluados consistieron en dos tipos de biosólidos (biosólidos de lagunas de oxidación (BLO) y biosólidos de lodos activados (BLA) y cuatro dosis de As (0, 25, 50, 100 mg kg-1), bajo condiciones de invernadero. La concentración de As se determinó por espectrometría de masas por plasma acoplado inductivamente (ICP-MS). A partir de la cuantificación de As se estimó el factor de translocación (FT) y el factor de bioacumulación (FB). El contenido de nitrógeno (N) total se cuantifico por el método de combustión. El fósforo (P) se analizó por colorimetría por el método de metavanadato, y el contenido de potasio (K), calcio (Ca), magnesio (Mg), cobre (Cu), manganeso (Mn), hierro (Fe) y zinc (Zn) que se cuantificaron por absorción atómica. Para porcentaje de aceite en la semilla se utilizó el método Soxhlet. La altura de planta y el peso seco de biomasa no variaron por efecto de tratamiento (P ≤ 0.05). El Factor de translocación (FT) y el Factor de bioconcentración (FBC) registraron rangos de 0.20 - 0.63 y 0.28 - 0.75, respectivamente. Las dosis aplicadas de As no afectaron la biomasa y absorción de nutrientes en la planta de higuerilla, lo cual indica que esta especie vegetal es tolerante a la toxicidad con potencial productivo en suelos contaminados con este elemento, en concentraciones hasta de 100 mg kg-1.

Abstract This study aimed to determine salivary concentrations of interleukin (IL)-1β, IL-2, IL-10, IL- 23, transforming growth factor (TGF)-β, tumor necrosis factor (TNF)-α, nitrate (a by-product of nitric oxide oxidation), and cortisol in patients with oral lichen planus (OLP). Twenty patients diagnosed with OLP and 20 sex-matched healthy volunteers (HV) were included in this cross-sectional study. Unstimulated whole saliva was collected in the morning. Salivary cytokine and cortisol concentrations were determined by enzyme-linked immunosorbent assays (ELISA). Nitrate was measured in a nitric oxide analyzer. We found higher salivary concentrations of IL-2 (p<0.003), IL-23 ( p<0.04), and TGF-β (p=0.05) in patients with OLP compared to HV. No significant differences were found in salivary levels of TNF-α, IL-1β, or IL-10. Nitrate concentrations were markedly increased in OLP patients (1,227.0 ± 738.8 µM/mg total protein) when compared to HV (261.6 ± 166.8 µM/mg; p<0.0001). Salivary cortisol levels were also higher in OLP patients (2.79 ± 1.39 vs. 1.94 ±1.21 ng/mg; p<0.048). The markedly increased salivary levels of nitric oxide in patients with OLP suggest a relationship of this molecule with the cell death and tissue damage observed in these lesions.

Resumen Este estudio tuvo como objetivo determinar las concentraciones salivales de interleucina (IL)-1β, IL-2, IL-10, IL-23, factor de crecimiento transformante (TGF)-β y factor de necrosis tumoral (TNF)-α, nitrato (subproducto de la oxidación del óxido nítrico) y cortisol en pacientes con liquen plano oral (OLP). En este estudio transversal se incluyeron veinte pacientes diagnosticados con OLP y 20 voluntarios sanos (HV) del mismo sexo. Saliva entera no estimulada Se recolectó por la mañana, se determinaron las concentraciones de citocinas y cortisol en saliva mediante ensayo inmunoabsorbente ligado a enzimas (ELISA), se determinó nitrato mediante un analizador de óxido nítrico, se encontraron concentraciones salivales mayores de IL-2 (p<0,003), IL- 23 (p<0,04) y TGF-β (p=0,05) en pacientes con OLP en comparación con HV. No se encontraron diferencias significativas en los niveles salivales de TNF-α, IL-1β e IL-10. Las concentraciones de nitrato fueron marcadamente aumentó en pacientes con OLP (1227,0 ± 738,8 µM/mg de proteína total), en comparación con HV (261,6 ± 166,8 µM/mg; p<0,0001). Los niveles de cortisol salival también fueron más altos en los pacientes con OLP que en los controles (2,79 ± 1,39 vs. 1,94 ±1,21 ng/mg; p<0,048). Los niveles de óxido nítrico en saliva aumentaron notablemente en pacientes con OLP, lo que sugiere una relación de esta molécula con la muerte celular y el daño tisular observado en las lesiones de OLP.

Abstract This study performed LSV simulation of two-step irreversible electron oxidation with the intermediate (E↓E), which was immobilized on the electrode surface. The response exhibited either one or two peaks, depending on the intermediate stability. The first electron transfer depended on the reactant diffusion, while the second one was a function of the accumulated intermediate. For this reason, the second Ip was higher than the first one, and the single peak split into two peaks, under the influence of an increased SR. Thermodynamic and kinetic parameters influence on the two components of the response were analyzed.

ABSTRACT The ancestral use of essential oils, obtained from various parts of plants, encompasses a wide range of purposes, including medicinal, flavoring, preserving, and aromatic uses. This research focused on conducting a comprehensive literature review on the use of essential oils in the sausage industry. A descriptive, inductive, and analytical approach was adopted, drawing on a variety of sources such as books, journals, technical regulations, theses, and scientific articles. The results of this study revealed that, out of the 92 technical documents (articles and theses) initially selected, 24 were excluded due to their age, leaving a total of 68 articles for the preparation of the technical document. Additionally, 21 documents were identified that provided specific information on the components and effects of essential oils in sausage manufacturing. In conclusion, it is highlighted that essential oils extracted from various plants, such as clove, rosemary, oregano, thyme, among others, have demonstrated their ability to prolong the shelf life of sausages by inhibiting the growth of pathogenic microorganisms and preventing lipid oxidation. Furthermore, it was observed that the application of these essential oils not only contributes to the preservation of meat products but also improves their organoleptic properties by imparting distinctive flavors and aromas.

RESUMEN El empleo ancestral de aceites esenciales, obtenidos de diversas partes de las plantas, abarca una amplia gama de propósitos, incluyendo usos medicinales, condimentarios, conservantes y aromatizantes. Esta investigación se centró en realizar una revisión bibliográfica sobre el uso de aceites esenciales en la industria de embutidos. Se adoptó un enfoque descriptivo, inductivo y analítico, recurriendo a una diversidad de fuentes como libros, revistas, normativas técnicas, tesis y artículos científicos. Los resultados de este estudio revelaron que, de los 92 documentos técnicos (artículos y tesis) inicialmente seleccionados, 24 fueron excluidos debido a su antigüedad, dejando un total de 68 artículos para la elaboración del documento técnico. Además, se identificaron 21 documentos que proporcionaron información específica sobre los componentes y efectos de los aceites esenciales en la fabricación de embutidos. Como conclusión, se destaca que los aceites esenciales extraídos de diversas plantas, como clavo, romero, orégano, tomillo, entre otros, han demostrado su capacidad para prolongar la vida útil de los embutidos al inhibir el crecimiento de microorganismos patógenos y prevenir la oxidación lipídica. Además, se observó que la aplicación de estos aceites esenciales no solo contribuye a la conservación de los productos cárnicos, sino que también mejora sus propiedades organolépticas al conferirles sabores y aromas distintivos.

In this study, the typical azo dye methyl orange (MO) was degraded by pyrite (FeS2) activated by hydrogen peroxide (H2O2). When [MO] = 0.1 mM, [FeSJ = 2.0 g/L and [H2O2] = 22 mM, 96.4% MO was removed in 120 min and the TOC removal rate was higher than 50%. HO* was the primary radical responsible for MO degradation, in addition, the acid condition promoted the degradation of MO in the FeS2/H2O2 system. MO in tap water and river water was not effectively degraded, whereas acidification could weaken the inhibitory effect on the FeS2/ H2O2 system to enable the degradation of MO in tap and river water. The OD600 indicated that the solution was environmentally friendly after the reaction, and three degradation pathways of MO were discussed. In summary, Fe(ll) could be dissolved from FeS2, which activated H2O2 to generate Fe(lll) and HO*. FeS2 could reduce Fe(lll) into Fe(ll), thus realizing the Fe(lll)/(ll) cycle and efficiently activating H2O2 to degrade MO.

ABSTRACT The elution by imidazole is used in the purification process of non-alpha IL-2 mutein, specifically in the immobilized metal chelates affinity chromatography step (IMAC). In order to demonstrate that a new elution process is possible using cheaper solutions, changes were made in the former capture step. These changes consist on separate the size exclusion chromatography and the controlled oxidation stage which are currently performed together, as well as changing the elution solution. To achieve this, a 22 factorial design of experiments was performed to evaluate the effect of pH and molar concentration on recovery, purity, and particle diameter. The best results were obtained with the solution of sodium acetate 20 mmol L-1 pH 4 being similar to those obtained in the industry nowadays: 29 % recovery, 90 % of purity, and particle diameter 18,40 nm. The first contribution of this paper is to demonstrate the feasibility of using the new elution methodology. Moreover, by using the academic software SuperPro Designer, the actual capture step of the purification process (elution by Imidazole) was simulated, validated, and verified. To demonstrate the relationship between costs and benefits, the CH SFF matrix gel volume was incremented. This change increased costs at this stage. However, the productivity obtained grew to 109 mg h-1, 2.78 times greater than the current productivity. Therefore, the gross net increased by 879 325,00 $. This result constitutes the second contribution of this paper.

RESUMEN La elución por Imidazol se utiliza en la etapa de captura del proceso de purificación de la muteína Interleukina-2 no alfa, específicamente en la cromatografía de afinidad de quelatos metálicos inmovilizados (IMAC). Para demostrar que es posible una nueva forma de elución en IMAC haciendo uso de soluciones menos costosas, se realizaron cambios en esta etapa: separar la cromatografía de exclusión molecular y la oxidación controlada (se realizan actualmente de forma conjunta), además de cambiar la solución de elución. Para lograr el objetivo, se realizó un diseño de experimentos factorial 22 evaluando el efecto del pH y la concentración molar en el recobrado, la pureza y el diámetro de partícula. Los mejores resultados se obtuvieron con la solución de acetato de sodio 20 mmol L-1 pH 4, siendo similares a los obtenidos hoy en la industria: 29 % de recobrado, 90 % de pureza y un diámetro de partícula de 18,40 nm. La primera contribución de este trabajo es demostrar la viabilidad de utilizar la nueva metodología de elución. Haciendo uso del software académico SuperPro Designer, se simuló, verificó y validó esta etapa. Con el propósito de demostrar la relación entre costos y beneficios, siendo la segunda contribución de este trabajo, se incrementó el volumen de gel de la matriz CH SFF. Este cambio resultó en un aumento de los costos en esta etapa. Sin embargo, la productividad obtenida creció en 109 mg h-1, siendo 2,78 veces mayor a la productividad actual, acrecentándose los ingresos en $ 879 325,00.

Abstract The flotation mechanism of galena with xanthate as the collector is generally explained based on the mixed potential of the pulp, in which an anodic electron transfer reaction from the collector to the mineral is combined with an O2 cathodic reduction. Sodium sulphide, often used as a mineral activator, strongly influences the pulp's mixed potential, and depending on the dosage applied, it can become a galena depressor reagent. In this way, the current study assesses galena flotability in the absence of collector, as well as in the presence of the collector potassium amyl xanthate (PAX) and sodium sulphide. The effect of an extremely cathodic potential was also studied through the addition of hydrogen peroxide. In addition, the effect of different stages in the oxidation of the galena surface on the flotability was investigated. Moreover, the zeta potential was measured and contact angle (wettability) tests were carried out. The contact angle measurements were taken for a distilled water, PAX solution and for a mixture of PAX and sodium sulphide solution on the oxidized and non-oxidized surface of galena. All the results showed that galena could be floated in all the PAX concentrations tested. It was observed that a moderate oxidation in the galena surface may contribute to an improvement of its flotation with PAX. However, extremely anodic and cathodic potentials cause flotability close to zero. The zeta potential results showed that sodium sulphide affected the interaction between PAX and galena. The measurements of the contact angle corroborated the results obtained in the microflotation tests. pulp O reduction activator pulps s applied reagent way (PAX peroxide investigated Moreover wettability (wettability out water nonoxidized non tested However zero