The use of materials such as organofunctionalized silica for application in solid phase extraction (SPE) allows the preconcentration of several ions, including Pt, and subsequent detection. This work aims to synthesize and characterize an organofunctionalized silica (Sil-TMSDT) with the silylant N’(trimethoxysilyl)propylethylenetriamine and its application as a solid phase in the preconcentration Pt4+ ions in aqueous media, using detection by flame atomization atomic absorption spectroscopy (FAAS). The Fourier-transform infrared spectroscopy (FTIR) spectra and scanning electron microscopy (SEM) coupled with energy-dispersive spectroscopy (EDS) confirmed the aminofunctionalization of the silica. For the adsorption process, a preconcentration mini-column with 200 mg of Sil-TMSDT, a solution of 0.485 mg L−1 of K2[PtCl6] at pH 10 and HNO3 0.5 mol L−1 as eluent were used, obtaining an enrichment factor of 15-fold with retention efficiency higher than 99%. The Pt4+ ion determined by FAAS showed a linear response between 0.02 and 0.40 mg L−1; a linear coefficient where R = 0.9981; a 16-fold preconcentration factor; a limit of quantification (LOQ) and limit of detection (LOD) of 0.045 and 0.014 mg L−1, respectively. The proposal system showed analytical applicability to determining Pt4+ ion in an aqueous medium and could be used to detect traces of this potentially toxic metal in biological fluids such as urine and blood. SPE (SPE Pt SilTMSDT Sil TMSDT (Sil-TMSDT Ntrimethoxysilylpropylethylenetriamine N trimethoxysilyl propylethylenetriamine Pt4 media FAAS. . (FAAS) Fouriertransform Fourier transform FTIR (FTIR SEM (SEM energydispersive energy dispersive EDS (EDS process minicolumn mini column 20 SilTMSDT, TMSDT, Sil-TMSDT 0485 0 485 0.48 L1 L 1 L− K2PtCl6 KPtCl K2 PtCl6 K PtCl K2[PtCl6 HNO 05 5 0. 15fold fold 15 99 99% 002 02 0.0 040 40 0.4 0.9981 09981 9981 16fold 16 LOQ (LOQ LOD (LOD 0045 045 0.04 0014 014 0.01 respectively blood (FAAS 2 048 48 K2PtCl K2[PtCl 9 00 04 4 0.998 0998 998 004 001 01 0.99 099 0.9 09

The species Oryza sativa (rice) and Musa cavendishii (banana) are sources of cellulose-rich waste biomass in the Amazon region, Tocantins State. This research investigates the nanoscale production of cellulose through the interactions between three choline amino acid ionic liquids Ch[AA]IL and the respective fibers by pretreatment. To this end, the synthesis of three ILs was carried out: choline arginate Ch[Arg], choline glycinate Ch[Gly] and choline lysinate Ch[Lys], characterized by Fourier transform infrared spectroscopy (FTIR). The samples resulting from the pretreatment were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). It was possible to infer from the SEM micrographs that Ch[Arg] caused greater fiber breakage than the other ILs. The TEM analyses identified fibers up to 16 nm in diameter. Positive effects were observed in the diffractograms, although no crystallinity was obtained in the pretreated samples. Thermogravimetry curves showed that the fibers treated with Ch[Arg] showed higher thermal stability. rice (rice banana (banana celluloserich rich region State ChAAIL Ch AA IL end out ChArg, ChArg Arg , ChGly Gly Ch[Gly ChLys, ChLys Lys Ch[Lys] FTIR. FTIR . (FTIR) SEM, (SEM) TEM, (TEM) Xray X ray XRD (XRD TGA. TGA (TGA) Ch[Arg 1 diameter diffractograms stability Ch[Lys (FTIR (SEM (TEM (TGA

The selective separation of precious metals from complex aqueous solutions is important in protecting the environment, aquatic ecosystems, water resources and recycling resources. In this study, cysteine-containing polymeric nanoparticles were synthesized using the molecular imprinting (MIP) technique with the mini-emulsion polymerization method. The basis of the polymer design is inspired by affinity of silver to cysteine in biological systems. The synthesized silver ion imprinted (Ag+-IIP) poly(hydroxyethylmethacrylate-N -methacryloyl-L-cysteine) poly(HEMA-MAC) nanoparticles were characterized by elemental analysis, zeta sizer, Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), and scanning electron microscopy (SEM). The effects of pH, ionic strength and interaction time on adsorption of Ag+ ions were investigated. In experimental studies, the highest adsorption amount (196.9 mg g1 nanoparticle) was reached in a short period of 40 min at pH 5.0 and 150 mg L-1 concentration. Selectivity studies of synthesized Ag+-IIP nanoparticles against silver (Ag+) ions were carried out in the presence of lithium (Li+), barium (Ba2+), mercury (Hg2+) and cadmium (Cd2+) ions. Experimental results indicate that nanoparticles adsorb Ag+ ions with high selectivity. Ag+-IIP nanoparticles have 3.7, 3.1, 2.4, and 2.6 times more selective or higher affinity for Ag+ ions compared to Li+, Ba2+, Hg2+ and Cd2+ ions, respectively, compared to Ag+-non-imprinted (NIP) nanoparticles. environment ecosystems study cysteinecontaining containing MIP (MIP miniemulsion mini emulsion method systems Ag+IIP AgIIP IIP Ag (Ag+-IIP polyhydroxyethylmethacrylateN poly hydroxyethylmethacrylate N methacryloylLcysteine methacryloyl L -methacryloyl-L-cysteine polyHEMAMAC HEMA MAC poly(HEMA-MAC analysis sizer FTIR (FTIR spectroscopy AFM, AFM , (AFM) SEM. SEM . (SEM) investigated 196.9 1969 196 9 (196. g nanoparticle 4 50 5 0 5. 15 L1 1 L- concentration (Ag+ Li Li+ (Li+) Ba2 Ba Ba2+ (Ba2+) Hg2 Hg (Hg2+ Cd2 Cd (Cd2+ selectivity 37 3 7 3.7 31 3.1 24 2 2.4 26 6 2. respectively Ag+nonimprinted Agnonimprinted non NIP (NIP (AFM (SEM 196. 19 (196 (Ag (Li+ (Ba2+ (Hg2 (Cd2 3. nonimprinted (19 (Li (Ba2 (Hg (Cd (1 (Ba (

Analysis of variance (ANOVA)-simultaneous component analysis (ASCA) is a method of choice for factorial design studies of environmental impacts on plant metabolomes and can be used to quantitatively carry out this comparative analysis. The impacts of seven mixture design extractor systems made up of ethanol, dichloromethane, and hexane and their 1:1 binary and 1:1:1 ternary solvents for several replicate experiments (n = 3, 4, 5) were assessed using ASCA models determined from Fourier-transform infrared (FTIR), near-infrared (NIR), and UV-Vis spectroscopic measurements on yerba mate leaf extracts. This analysis considered two-factor effects: secondary sexual dimorphism (male and female plants) and cultivation systems (monoculture and agroforestry), as well as their interaction effect. The three binary solvents were found to be more efficient extractor systems for all four detectors as they found 83 main and interaction effects significant at or above the 95% confidence level compared with only 47 for the pure solvent extracts. Binary solvent extracts resulted in averages between 44.04 and 86.61% for the ASCA total effect variances compared with 40.62 to 71.07% for pure extractors. Of the 60 significant effects found for experiments with 5 repetitions 53 or 88% were obtained with only triplicate determinations. The choice of spectroscopic technique and solvent system have large impacts on metabolomic analysis results. ANOVAsimultaneous ANOVA simultaneous (ASCA ethanol dichloromethane 11 1 1: 111 1:1: n 3 4 Fouriertransform Fourier transform FTIR, FTIR , (FTIR) nearinfrared near NIR, NIR (NIR) UVVis UV Vis twofactor two factor male plants monoculture agroforestry, agroforestry agroforestry) 8 95 4404 44 04 44.0 8661 86 61 86.61 4062 40 62 40.6 7107 71 07 71.07 extractors 6 88 determinations results (FTIR (NIR 9 440 0 44. 866 86.6 406 40. 710 7 71.0 86. 71.

Poly(amidoamine)-type dendrimers (PAMAM) were synthesized by divergent routes, and generations (G0.5, G1.0, G1.5, G2.0 and G2.5) along with hydroxylated half-generation polymers (G0.5-OH, G1.5-OH and G2.5-OH) were characterized by Fourier-transform infrared spectroscopy, thermogravimetric analysis and differential scanning calorimetry. Carbon dioxide (CO2) capture tests were performed using thermogravimetric analysis. Among the absorption temperatures tested, 60 °C was the most promising: 0.77, 1.08, and 1.14 mol CO2 L 1 for G0.5-OH, G1.5-OH and G2.5-OH, respectively, of CO2 and partial pressure of 45 kPa. This showed that dendrimers with larger molecular structures have more hydroxyl groups and consequently capture more CO2. However, at low partial pressures (< 2 kPa), CO2 solubility in PAMAM increased with temperature reduction, confirmed by Henry’s solubility constant (398.4 mol m3 kPa 1, in G2.5-OH at 40 °C). According to the thermodynamic properties of CO2 solubilization, the process was spontaneous (∆Gsol < 0) and exothermic (∆Hsol < 0). Polyamidoaminetype Poly amidoamine type (PAMAM routes G0.5, G05 G G0 5 (G0.5 G10 G1 0 G1.0 G15 G1.5 G20 G2 G2. G2.5 G25 halfgeneration half generation G0.5OH, G05OH GOH G0.5 OH, OH (G0.5-OH G1.5OH G15OH G2.5OH G25OH Fouriertransform Fourier transform spectroscopy calorimetry CO (CO2 tested 6 C promising 077 77 0.77 108 08 1.08 114 14 1.1 G0.5-OH G2.5OH, respectively 4 However ( kPa, , kPa) reduction Henrys Henry s 398.4 3984 398 (398. m °C. . °C) solubilization ∆Gsol Gsol ∆Hsol Hsol 0. (G0. G1. 5OH G0.5OH G0. (CO 07 7 0.7 10 1.0 11 1. 398. 39 (398 (G0 3 (39 (G (3

The metal-organic frameworks (MOFs) UiO-66-NH2, UiO-66-2,5-(OH)2, UiO-66-NO2, UiO-66-NDC, and UiO-66-BPDC were synthesized under solvothermal conditions using different functionalized organic linkers. The structures and properties of the samples were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, and nitrogen adsorption-desorption isotherms. The crystal structures of these functionalized UiO-66(Zr) forms were similar. A series of functionalized UiO-66(Zr) samples were used in the adsorption of carbon dioxide (CO2). UiO-66-NH2 had the highest CO2 adsorption capacity (about 3.35 mmol g-1) due to its small polar -NH2 group. The performance of UiO-66-NH2 in CO2 adsorption at different temperatures was also determined. The amino-functionalized material possessed better adsorption properties at 273 K than at 303 K, while the CO2 working capacity of UiO-66-NH2 was fully recovered after cyclic regeneration. metalorganic metal MOFs (MOFs UiO66NH2, UiO66NH2 UiONH UiO 66 NH2, NH2 NH UiO662,5OH2, UiO6625OH2 UiOOH 2,5 OH 2, 2 5 UiO-66-2,5-(OH)2 UiO66NO2, UiO66NO2 UiONO NO2, NO2 NO UiO-66-NO2 UiO66NDC, UiO66NDC UiONDC NDC, NDC UiO-66-NDC UiO66BPDC UiOBPDC BPDC linkers Xray X ray diffraction spectroscopy analysis microscopy adsorptiondesorption desorption isotherms UiO66Zr UiOZr Zr UiO-66(Zr similar CO2. CO . (CO2) UiO-66-NH about 335 3 35 3.3 g1 g 1 g-1 -NH group determined aminofunctionalized amino 27 30 regeneration UiO66NH 6 UiO662 5OH2 UiO662,5OH2 UiO6625OH 25 UiO-66-2,5-(OH) UiO66NO UiO-66-NO (CO2 33 3. g- UiO66 5OH UiO662,5OH UiO-66-2,5-(OH (CO UiO6

Chitosan (CS) blends with collagen (CL) and Aloe vera (AV) have gained significant attention in the biomedical field due to their biocompatibility, biodegradability, and potential for wound healing applications. In this study, we investigated the preparation and characterization of CS/CL and CS/AV blends using selective precipitation and co-precipitation techniques. The synthesis processes were analyzed for yield and 4-hydroxyproline content (in CS/CL blends). The materials were characterized using bromatological analyses, viscosity measurements, Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM). These eco-friendly methods effectively promoted interactions between the biopolymers, resulting in homogeneous blends with tunable properties. Besides, they are simple, fast, safe, and require minimal infrastructure. This study demonstrated that selective precipitation and co-precipitation are effective methods for producing chitosan/collagen and chitosan/Aloe vera blends. These methods foster interactions and miscibility between the biopolymers, as confirmed by FTIR, XRD, viscosity, and 4-Hy content analyses. They also align with green chemistry principles by avoiding organic solvents, reducing environmental risks, and minimizing waste. The high yields achieved, especially for CS/AV blends (exceeding 96%), make these materials compatible with lyophilization procedures. The absence of segregated phases after appropriate washing underscores their suitability for pharmaceutical formulations and other applications. CS (CS CL (CL AV (AV biocompatibility biodegradability applications CSCL CSAV coprecipitation co techniques 4hydroxyproline hydroxyproline 4 . blends) analyses measurements Fouriertransform Fourier transform FTIR , (FTIR) Xray X ray XRD (XRD) SEM. SEM (SEM) ecofriendly eco friendly biopolymers properties Besides simple fast safe infrastructure chitosancollagen chitosan chitosanAloe 4Hy Hy solvents risks waste achieved exceeding 96%, 96 96% 96%) procedures (FTIR (XRD (SEM 9

Acetic acid bacteria (AAB) are versatile organisms that catalyze the conversion of a wide range of carbon sources into biomolecules of great industrial interest. In this study, we exploited the ability of Gluconobacter spp. to synthesize levans. Among the isolated strains, Gluconobacter cerinus UELBM11 produced approximately 14.0 g L−1 of levan under non-optimized conditions. Gas chromatography-mass spectrometry (GC-MS), Fourier transform infrared spectroscopy (FTIR), and nuclear magnetic resonance (NMR) analyses confirmed that levan obtained from G. cerinus UELBM11 consisted of a β-(2→6)-D-fructose backbone with some β-(2→1) ramifications. The average molecular weight (Mw) of the purified levan was 8.78 × 105 Da. Thermogravimetric/differential thermogravimetric (TGA/DTG) analysis indicated high thermal stability, with the maximum decomposition rate observed at 227.44 °C. Scanning electron microscopy (SEM) revealed a microporous morphology, and the antioxidant activity assays demonstrated that levan had a high scavenging capacity of 2,2’-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) and hydroxyl radicals. Therefore, it has been demonstrated the levan produced by G. cerinus UELBM11 is a promising natural antioxidant and, owing to its microporosity and excellent thermal properties and stability, is a potential candidate as an additive in cosmetics, pharmaceuticals, and food products. AAB (AAB interest study spp levans strains UELBM UELBM1 140 14 0 14. L1 L 1 L− nonoptimized non optimized conditions chromatographymass chromatography mass GCMS, GCMS GC MS , (GC-MS) FTIR, FTIR (FTIR) NMR (NMR G β2→6Dfructose β26Dfructose βDfructose β 2→6 D fructose 2 6 β2→1 β21 2→1 β-(2→1 ramifications Mw (Mw 878 8 78 8.7 10 Da Thermogravimetricdifferential Thermogravimetric differential TGA/DTG TGADTG TGA DTG (TGA/DTG stability 22744 227 44 227.4 C °C SEM (SEM morphology 2,2azinobis 22azinobis azinobis 2,2 azino bis 3ethylbenzothiazoline6sulfonic ethylbenzothiazolinesulfonic 3 ethylbenzothiazoline sulfonic ABTS (ABTS radicals Therefore cosmetics pharmaceuticals products (GC-MS (FTIR β2 6Dfructose Dfructose 26 2→ β2→ 21 β-(2→ 87 7 8. 2274 22 4 227. 2azinobis 2, β-(2 β-( β-

The present work aims to extract and test cashew nut peel oil as a natural antioxidant in the oxidative stabilization of biodiesel. Therefore, determinations of the ideal time of Soxhlet and thermal extractions, Fourier transform infrared spectroscopy (FTIR) analyses, and evaluation of the oxidative stability by Rancimat method were carried out. FTIR analyses revealed that the 3rd cycle of extraction was sufficient to extract all the oil, with an average yield of 30.0%. For the thermal extraction of the laboratory technical cashew nut peel oil, the best extraction, based on statistical analysis, was 60 min, yielding 20.0%. The FTIR analysis of the extracted cashew nut peel oil showed characteristic peaks of phenolic groups and organic acids, showing differences in the intensities of the absorption bands. The oxidative stability showed induction period of 8 h 40 min for the hydraulic press extraction, 10 h 35 min for the Soxhlet extraction, and 10 h 65 min for the industrial technical extraction of the cashew nut peel oil. All values were below the 12-h limit established by the National Agency for Petroleum, Natural Gas and Biofuels (ANP). The technical cashew nut peel oil extracted in the laboratory presented an induction period of 11 h 12 min, close to that recommended by ANP, proving to be a promising natural antioxidant. Cardanol presented satisfactory results with 25 h 22 min, double that suggested by ANP. Thus, cashew nut peel oil showed important and promising results as a natural antioxidant for biodiesel. biodiesel Therefore extractions (FTIR out rd 300 30 0 30.0% 6 200 20 20.0% acids bands 4 1 3 12h Petroleum ANP . (ANP) 2 Thus 30.0 20.0 (ANP 30. 20.

Efavirenz, an antiretroviral drug, is a class 2 according to the biopharmaceutics classification system. Many dissolution enhancement systems have been tried and our group had success using wet milling to decrease particle size and granules were obtained by spray and freeze drying. In this paper we present data related to the upgrade in the process, raising the solids concentration in the suspension from 10 to 50% (m/v) and changing the drying step for a fluid bed granulation. After that, tablets were obtained. Granules and tablets were fully evaluated and a pharmacokinetic study was also performed with the granules. By powder X-ray diffraction (PXRD) and Fourier transform infrared spectroscopy (FTIR) it was possible to prove that there was no phase transition in the sample after milling and drying. Dissolution efficiency of 4 from 5 granules was higher than 90%, considering 83% for the raw material. Tablets were technically approved but the dissolution was impacted and just 2 out of 11 showed results > 80%. A high enhancement in the bioavailability was also observed, around 172%. So, it is possible to conclude that efavirenz microcrystals with enhanced dissolution and bioavailability can be formulated into tablets and are a viable system to develop a new drug product. Efavirenz process 1 50 m/v mv m v (m/v granulation Xray X ray PXRD (PXRD FTIR (FTIR 90 90% 83 material 80 80% observed 172 172% So product 9 8 17

This study highlights the synthesis of innovative polyurethane materials derived from Moringa oleifera oils extracted from two distinct sources. The oils were converted into their respective polyols through the in situ generated performic acid method. Diverse material characteristics were observed due to different agroclimatic and cultivation conditions for the sources. Extraction yields were 45.21% (source 1) and 40.32% (source 2), with acid values of 28.70 and 26.00 mg KOH per g of oil, respectively. Oleic acid constituted 79.87 and 67.11% of the oils composition, respectively. Nuclear magnetic resonance and Fourier transform infrared spectroscopy (FTIR) confirmed the hydroxylation of the oils. FTIR also identified the isocyanate structures in the synthesized polyurethane materials. Gel permeation chromatography analysis revealed a higher oligomer content in the polyol synthesized from the oil extracted from source 2. Thermogravimetric analysis demonstrated enhanced thermal stability post-oil conversion, highlighting decomposition stages for rigid and flexible segments. Differential scanning calorimetry indicated higher unsaturation in the oil extracted from source 1, resulting in an elevated crystallization temperature. Tensile testing showed increased elasticity as the [NCO]/[OH] ratio decreased in the material, emphasizing the influence of polyol and crosslinking agent concentrations on mechanical resistance of polyurethane materials. sources method 4521 45 21 45.21 1 4032 40 32 40.32 2, 2 , 2) 2870 28 70 28.7 2600 26 00 26.0 respectively 7987 79 87 79.8 6711 67 11 67.11 composition (FTIR postoil post conversion segments temperature NCO/OH NCOOH NCO / OH [NCO]/[OH 452 4 45.2 403 3 40.3 287 7 28. 260 0 26. 798 8 79. 671 6 67.1 45. 40. 67.

Nanocomposites of GO/γ-Fe2O3 were used for magnetic dispersive solid-phase microextraction (m-d-μ-SPE) of six pesticides from river water samples, followed by the determination using high performance liquid chromatography-diode array detection. The synthesis of the nanocomposites is described and characterized using Fourier transform-infrared spectroscopy, X-ray diffraction, and scanning electron microscopy. A central composite design was used to optimize the extraction time, sample solution pH, and adsorbent amount. The solvent type and volume for desorption and the effect of the ionic strength for adsorption were also investigated. The optimum adsorption conditions were achieved at 84 min of extraction time, pH 5.4, 115 mg of absorbent, and 1% (m/v) of NaCl, while the desorption solvent selected was 1.0 mL of methanol-acetic acid (9:1, v/v). The limits of detection ranged from 0.1 to 0.9 μg L-1, and a good precision was achieved with relative standard deviation (RSD) lower than 7.6% (n = 10). The accuracy of the method was accessed by recovery tests ranging from 82 to 117% (n = 3, RSD < 8%). GO/γFe2O3 GOγFe2O3 GOγFeO GO/γ Fe2O3 GO γ Fe O GO/γ-Fe2O solidphase solid phase mdμSPE m d μ SPE (m-d-μ-SPE samples chromatographydiode chromatography diode transforminfrared transform infrared spectroscopy Xray X ray diffraction microscopy time amount investigated 8 54 5 4 5.4 11 absorbent 1 m/v mv v (m/v NaCl 10 0 1. methanolacetic methanol acetic 91, 91 9 1, (9:1 v/v. vv v/v . v/v) 01 0. 09 L1, L1 L L-1 (RSD 76 7 6 7.6 n 10. 10) 117 3 8%. 8% 8%) γFe2O3 γFe GO/γFe2O GOγFe GOγFe2O GOγ FeO Fe2O 5. (9: L- 7. γFeO γFe2O (9 (

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

This study investigated the removal of contaminants in water by adsorption on thermoplastic starch (TPS) and kraft lignin (KL) composites. A study on the desorption of methylene blue (MB) and methyl orange (MO) dyes in water was also carried out, followed by the photodegradation of solutions containing dissolved dyes. Initially, the surface morphology of the TPS and TPS-KL films was analyzed by scanning electron microscopy, revealing advantageous characteristics for efficient adsorption of contaminants. Fourier transform infrared spectroscopy (FTIR) analysis made it possible to characterize the TPS and TPS-KL composites. The results demonstrate the reversibility of the process and confirm the lack of permanent chemical modification in the polymer matrix, indicating that the adsorption/desorption process is physical rather than chemical. This suggests that the adsorbent material can be reused without losing its fundamental structural properties. Furthermore, the study allows for verification of the chemical changes on the surfaces of the materials involved. Ultraviolet-visible spectroscopy (UV-Vis) results show that for MO, both substrates exhibited low adsorption capacity, with efficiency values close to 20%. In contrast, for MB, both composite materials displayed excellent dye adsorption rates, achieving efficiencies of 78% or higher. The photodegradation of adsorbed dyes revealed promising results. (TPS KL (KL composites MB (MB MO (MO out Initially TPSKL microscopy FTIR (FTIR matrix adsorptiondesorption properties Furthermore involved Ultravioletvisible Ultraviolet visible UVVis UV Vis (UV-Vis capacity 20 20% contrast rates 78 higher 2 7

Abstract Introduction. Weeds are one of the main problems in agricultural productivity due to their interactions with crops, such as alelopatic effects on germination. Objective. To evaluate the allelopathy of kikuyo grass (Cenchrus clandestinus) on the germination of beans (Phaseolus vulgaris L.) variety ICA Cerinza. Materials and methods. The study was conducted at the Quality Control Laboratory of the Universidad de Pamplona, Central Campus, Pamplona, Norte de Santander, Colombia, from May to August 2022. To each experimental unit (Petri dishe) with 12 been seeds, 6 mL of kikuyo aqueous extract (leaf, stem, and root) at three concentrations (1, 2.5, and 5 %), plus a control (0 %), were added, totaling 12 treatments. From day 0 to 12, the number of germinated seeds (NGS) was recorded, and the germination rate index (GRI) and germination index (IG) were calculated. The biomolecular profile of the aqueous extract was determined using the Fourier-transform spectroscopy. A completely randomized experimental design with a factorial arrangement (3x4), with repeated measures in each experimental unit, was employed. The intersuject factors were the organ type and concentration, while the intrasubject factor was the evaluation time (12 days). Results. Significant differences (p<0.001) were observed for NSG among treatments due to the concentration of the aqueous extract, as well as for IG, while GRI depended on the organ (p<0.05) and concentration (p<0.001), both negatively affected as the concentration increased. The infrared spectrum of the extract determined the presence of polyphenols, nitriles, and siloxanes. Conclusión. C. clandestinus affected NGS, GRI, and GI of P. vulgaris, with an allelopathic effect of the leaf aqueous extract at higher concentrations. Polyphenols, nitriles, and siloxanes associated with allelopathic effects were identified in the aqueous extracts.

Resumen Introducción. Las arvenses son uno de los principales problemas en la productividad agrícola, debido a interacciones con el cultivo, como efectos alelopáticos sobre la germinación. Objetivo. Evaluar la alelopatía del pasto kikuyo (Cenchrus clandestinus) en la germinación de frijol (Phaseolus vulgaris L.) variedad ICA Cerinza. Materiales y métodos. El estudio se realizó en el laboratorio de Control de Calidad de la Universidad de Pamplona, Campus Central, Pamplona, Norte de Santander, Colombia, en mayo-agosto 2022. A cada unidad experimental (caja de Petri) con doce semillas de frijol se le agregó 6 mL de extracto acuoso de kikuyo (hoja, tallo y raíz) en tres concentraciones (1, 2,5 y 5 %), más un testigo (0 %), para un total de doce tratamientos. En el lapso de 0 a 12 días, se registró el número de semillas germinadas (NSG), se calculó el índice de tasa de germinación (ITG) y el índice de germinación (IG), y se determinó el perfil biomolecular del extracto acuoso mediante la técnica de espectroscopia transformada de Fourier. Se utilizó un diseño experimental completamente al azar con arreglo factorial (3x4), con medidas repetidas en cada unidad experimental. Los factores intersujetos fueron el tipo de órgano y concentración, y el factor intrasujeto fue el tiempo (12 días) de evaluación. Resultados. Se observaron diferencias significativas (p<0,001) para NSG entre tratamientos por efecto de la concentración del extracto acuoso al igual que para IG, mientras que ITG dependió del órgano (p<0,05) y la concentración (p<0,001); ambos fueron afectados de forma negativa conforme aumentó la concentración. En el espectro infrarrojo del extracto se determinaron polifenoles, nitrilos y siloxanos. Conclusión. C. clandestinus afectó NSG, el ITG e IG de P. vulgaris, con efecto alelopático del extracto acuoso de hoja en mayor concentración. En los extractos acuosos se determinaron polifenoles, nitrilos y siloxanos, asociados a efecto alelopático.