Abstract (Introduction): The current cultivation of trees is insufficient to cover the national demand for wood, in this way small producers become an alternative solution to this situation, since despite having small areas, in the country there are abundant farms with these conditions; However, the current forest management scheme does not meet adequate standards for the incorporation of these small producers. (Objective): To present an adaptive forest management scheme (AFMS) to the needs of the small farmer, in addition, to demonstrate the institutional availability to change according to expert criteria. (Methodology): 1) the factors that influence the decision to adopt an agricultural or forestry production system were identified; 2) a profile of an ideal productive system that met the interests and preferences of the small producer was made, which was compared with the characteristics of agricultural and forestry production; 3) the proposal of an EMFA adjusted to the preferences and interest of the producer was made, which was also compared with the ideal profile; 4) three proposed change actions were presented to experts, obtaining different degrees of possibility of changes in the EMFA. (Results): The discrepancy of the forest management scheme for the cultivation of trees with the perspective that a small producer has on an ideal production system was evidenced, as well as the substantial improvement that an EMFA would have in the valuation of the small producer and the institutional availability to change the EMFA according to the perspective of the small producers. (Conclusions): The adjustment of the forest management scheme allows a greater adoption of the activity by the small producer, but it was recognized that any proposal that is made would be successful only if forest governance makes it more flexible and allows change.

Resumen (Introducción): El cultivo actual de árboles es insuficiente para cubrir la demanda nacional de madera, de este modo, los pequeños productores se tornan como una alternativa de solución ante esta situación, ya que pese a contar con áreas pequeñas, en el país son abundantes las fincas con estas condiciones; sin embargo, el esquema actual de manejo forestal no cumple con estándares adecuados para la incorporación de estos pequeños productores. (Objetivo): Presentar un esquema de manejo forestal adaptativo (EMFA) a las necesidades del pequeño productor, además de evidenciar la disponibilidad institucional al cambio, según el criterio experto. (Metodología): 1) se identificaron los factores que influyen en la decisión de adopción de un sistema productivo agrícola o forestal; 2) se realizó un perfil de un sistema productivo ideal que cumpliera con los intereses y preferencias del pequeño productor, el cual se confrontó con las características de la producción agrícola y forestal; 3) se efectuó la propuesta de un EMFA ajustado a las preferencias e interés del productor, que fue también confrontada con el perfil ideal; 4) se expusieron tres acciones de cambio propuestas ante expertos, obteniendo diferentes grados de posibilidad de cambios en el EMFA. (Resultados): Se evidenció la discrepancia del esquema de manejo forestal para el cultivo de árboles con la perspectiva que un pequeño productor tiene sobre un sistema de producción ideal, asimismo la mejora sustancial que un EMFA tendría en la valoración del pequeño productor y la disponibilidad institucional al cambio del EMFA, según la perspectiva de los pequeños productores. (Conclusiones): El ajuste del esquema de manejo forestal permite una mayor adopción del cultivo de árboles por parte del pequeño productor, pero se reconoció que cualquier propuesta que se realice lograría ser exitosa si la gobernanza forestal flexibiliza y posibilita el cambio.

Abstract This study investigated the effect of dolomitic lime incorporation on the microstructure and mechanical properties of metakaolin-based geopolymers activated by alkaline solution. Five geopolymer mixtures were prepared with the addition of 0.0%, 2.5%, 5.0%, 7.5%, and 10.0% dolomitic lime. The microstructure of the geopolymers was evaluated by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction analyses (XRD). The compressive strength of the mixtures ranged between 53.2 and 63.0 MPa after 28 days of ambient curing. SEM/EDS analyses showed that the main phases formed were the N-A-S-H gel together with the C-A-S-H and N-M-A-S-H gels in the mixtures with dolomitic lime. In summary, the results showed that the incorporation of dolomitic lime can significantly improve the microstructure and properties of geopolymers. metakaolinbased metakaolin based solution 00 0 0.0% 25 2 5 2.5% 50 5.0% 75 7 7.5% 100 10 10.0 SEM, SEM , (SEM) energydispersive energy dispersive Xray X ray EDS, EDS (EDS) XRD. XRD . (XRD) 532 53 53. 630 63 63. curing SEMEDS NASH N A S H CASH C NMASH M summary 0.0 2.5 5.0 7.5 1 10. (SEM (EDS (XRD 6 0. 2. 5. 7.

Resumo Este estudo investigou o efeito da incorporação de cal dolomítica na microestrutura e nas propriedades mecânicas de geopolímeros à base de metacaulim ativados por solução alcalina. Foram preparadas cinco misturas de geopolímeros com adição de 0,0%, 2,5%, 5,0%, 7,5% e 10,0% de cal dolomítica. A microestrutura dos geopolímeros foi avaliada por microscopia eletrônica de varredura (MEV), espectroscopia de energia dispersiva de raios X (EDS) e análises de difração de raios X (DRX). A resistência à compressão das misturas variou entre 53,2 e 63,0 MPa após 28 dias de cura ambiente. As análises SEM/EDS mostraram que as principais fases formadas foram o gel N-A-S-H juntamente com os géis C-A-S-H e N-M-A-S-H nas misturas com cal dolomítica. Em resumo, os resultados mostraram que a incorporação de cal dolomítica pode melhorar significativamente a microestrutura e as propriedades dos geopolímeros. alcalina 00 0 0,0% 25 2 5 2,5% 50 5,0% 75 7 7,5 100 10 10,0 MEV, MEV , (MEV) EDS (EDS DRX. DRX . (DRX) 532 53 53, 630 63 63, ambiente SEMEDS SEM NASH N S H CASH C NMASH M resumo 0,0 2,5 5,0 7, 1 10, (MEV (DRX 6 0, 2, 5,

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 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 (

Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by extracellular accumulation of amyloid-β (Aβ) peptides in the brain. This study demonstrates the direct association of the disposable pipette extraction (DPX) with tandem mass spectrometry (MS/MS) for the analysis of Aβ peptides in cerebrospinal fluid (CSF) samples. Different parameters were optimized in order to improve detectability in the MS/MS including mobile phase percentage of ammonium hydroxide, mobile phase flow rate and acquisition mode. Also, this method used an electrospray ionization (ESI) low-flow probe and direct infusion of an organic solution in the MS/MS. The DPX-MS/MS method showed adequate linearity for determining Aβ peptides in CSF-linearity ranged from 0.1 to 1.5 ng mL 1. The coefficients of determination were higher than 0.99; the precision coefficient of variation (CV) ranged from 0.3 to 12.7%; and the accuracy relative standard deviation (RSD) ranged from -13.6 to 13.2%. Alzheimers Alzheimer s AD (AD amyloidβ amyloid β (Aβ brain DPX (DPX MSMS MS (MS/MS CSF (CSF samples hydroxide mode Also ESI (ESI lowflow low DPXMS/MS DPXMSMS CSFlinearity 01 0 1 0. 15 5 0.99 099 99 CV (CV 03 3 12.7% 127 12 7 RSD (RSD 13.6 136 13 6 -13. 132 2 13.2% DPXMS 0.9 09 9 12.7 13. -13 13.2 12. -1 -

In the water/triethanolamine/ethanol system, TiCl4 aqueous solution is used as the precursor to regulate the conversion rate of TiCl4 by changing the reaction temperature, water volume, pH value, and ethanol amount. The experiment uses a single-factor method to investigate the dynamic relationship between Ti4+ concentration and time under various factors, thereby achieving controllable TiO2 production. The experimental results showed that under a single factor, the conversion rate showed a trend of first steep and then slow growth within 180 min. After 180 min, the conversion rate tended to stabilize. Considering various factors, it was found that VTiCl4:VC6H15NO3:VH2O:VC2H5OH = 1:6:15:30, pH = 7, reaction time at room temperature was 4 h, and the hydrolysis effect was good. The final conversion rate was 90.46%, and the hydrolysis reaction conforms to the first-order reaction equation. Kinetic parameters: pre-factor (A) = 0.107, activation energy (Ea) = 4488.65 J mol-1. watertriethanolamineethanol triethanolamine system TiCl volume value amount singlefactor factor Ti4 Ti factors TiO production 18 min stabilize VTiCl4VC6H15NO3VH2OVC2H5OH VTiClVCHNOVHOVCHOH VTiCl4 VC6H15NO3 VH2O VC2H5OH VTiCl VC H NO VH O OH 161530, 161530 1 6 15 30, 30 1:6:15:30 7 h good 9046 90 46 90.46% firstorder order equation parameters prefactor pre A (A 0107 0 107 0.107 Ea (Ea 448865 4488 65 4488.6 mol1. mol1 mol 1. mol-1 OVC VCHNO VC6H15NO VHO VCHOH 16153 3 1:6:15:3 904 9 90.46 010 10 0.10 44886 448 4488. mol- 1615 1:6:15: 90.4 01 0.1 44 161 1:6:15 90. 0. 16 1:6:1 1:6: 1:6 1:

The rapid advance of nanotechnology has led to the proliferation of a wide range of water-soluble nanomaterials and therefore, a profound impact on the environment, underscoring the need to devise effective methods for isolating and confining these nanomaterials. This study presents the development of a highly effective system capable of removing and storing gold nanoparticles in solution using modified resins with different linking groups, such as tris(2-aminoethyl) amine, 3-mercaptopropionic acid, 11-mercaptoundecanoic acid, and L-cysteine. The catalytic properties of the resins functionalized with the thiol group containing gold nanoparticles were evaluated, using the reduction of the nitro compounds (3,5-dinitrosalicylic acid, 4-nitroguaiacol and 4-nitroaniline) as model reaction. Solid-phase organic synthesis was employed to prepare the modified resins and their interaction with gold nanoparticles was characterized using infrared spectroscopy, thermogravimetric analysis, field emission scanning electron microscopy-energy dispersive spectroscopy, and X-ray photoelectron spectroscopy. The removal capacity of the resins was evaluated using ultraviolet-visible optical emission spectroscopy and inductively coupled plasma techniques. Ultraviolet-visible technique was suitable to assess the catalytic properties of the functionalized resins containing gold nanoparticles. It was determined that the functionalized resins showed remarkable capacity for complex gold nanoparticles, removing them from the solution. The most significant removal was with 11-mercaptoundecanoic acid. watersoluble water soluble therefore environment groups tris2aminoethyl trisaminoethyl tris 2 aminoethyl tris(2-aminoethyl amine 3mercaptopropionic mercaptopropionic 3 acid 11mercaptoundecanoic mercaptoundecanoic 11 Lcysteine. Lcysteine L cysteine. cysteine L-cysteine 3,5dinitrosalicylic 35dinitrosalicylic dinitrosalicylic 3,5 5 4nitroguaiacol nitroguaiacol 4 4nitroaniline nitroaniline 4-nitroaniline reaction Solidphase Solid phase analysis microscopyenergy microscopy energy Xray X ray ultravioletvisible ultraviolet visible techniques Ultravioletvisible Ultraviolet 1 5dinitrosalicylic 35 3,

RESUMO A estruvita (NH4MgPO4∙6H2O) é um fertilizante de liberação lenta obtido através da recuperação de fósforo e/ou nitrogênio de águas residuais geralmente pela adição de sais de magnésio. Neste sentido, objetivou-se avaliar a viabilidade da substituição de fontes comerciais de magnésio por fontes alternativas no processo de precipitação de estruvita, em termos de remoção de amônio e fosfato, e quantificação e caracterização do cristal precipitado. Os experimentos foram conduzidos em escala de bancada sob delineamento inteiramente casualizado a pH 9,5 através da precipitação de uma solução de efluente sintético com quatro diferentes fontes de magnésio: MgCl2∙6H2O, MgSO4∙7H2O, MgO e magnesita (MgCO3). Após pré-acidificação, soluções derivadas de fontes alternativas de baixo custo de magnésio removeram acima de 55 e 90% de nitrogênio amoniacal e fosfato em solução, respectivamente, e alcançaram por volta de 10 g L-1 de cristais precipitados. A proximidade dos resultados obtidos com soluções derivadas de fontes comerciais de magnésio (46ꟷ56% de remoção de nitrogênio amoniacal, 97% de remoção de fosfato, e mais de 6 g L-1 de precipitado formado) indicou que reagentes alternativos puderam facilmente substituir os comerciais se submetidos ao prévio processo de digestão, a fim de tornar o magnésio disponível em solução. A análise qualitativa por difratometria de raios-X confirmou a presença de estruvita e newberyita na maioria dos precipitados. NH4MgPO4∙6H2O NH4MgPO46H2O NHMgPOHO NH4MgPO4 6H2O NH MgPO H O (NH4MgPO4∙6H2O eou ou sentido objetivouse objetivou 95 9 5 9, MgCl26H2O MgClHO MgCl2 MgCl MgCl2∙6H2O MgSO47H2O MgSOHO MgSO4 7H2O MgSO MgSO4∙7H2O MgCO3. MgCO3 MgCO . (MgCO3) préacidificação, préacidificação pré acidificação, acidificação pré-acidificação 90 respectivamente 1 L1 L L- precipitados 46ꟷ56% 46ꟷ56 ꟷ (46ꟷ56 97 formado digestão raiosX raios X NHMgPO NH4MgPO HO (MgCO3 46ꟷ5 (46ꟷ5 (MgCO 46ꟷ (46ꟷ

ABSTRACT Struvite (NH4MgPO4∙6H2O) is a slow-release fertilizer obtained through phosphorus and/or nitrogen recovery from wastewaters, usually by adding magnesium salts. In this sense, the aim was to evaluate the viability of replacing commercial magnesium sources with alternative ones in the struvite precipitation process regarding ammonium and phosphate removal and precipitated crystal quantification and characterization. Experiments were conducted on a bench scale in a completely randomized design at pH 9.5 by precipitation of synthetic wastewater solution with four magnesium sources: MgCl2∙6H2O, MgSO4∙7H2O, MgO, and magnesite (MgCO3). After pre-acidification, derived solutions from low-cost alternative sources of magnesium removed above 55 and 90% of ammonium nitrogen and phosphate in solution, respectively, and reached around 10 g L-1 of precipitated crystals. Results proximity obtained with solutions derived from commercial sources of magnesium (46ꟷ56% of ammonium nitrogen removal, 97% of phosphate removal, and more than 6 g L-1 of precipitate formed) indicated that alternative reagents could easily substitute commercial ones if submitted to the previous digestion process, making magnesium available in solution. Qualitative analysis by X-ray diffraction confirmed the presence of both struvite and newberyite in most precipitates. NH4MgPO4∙6H2O NH4MgPO46H2O NHMgPOHO NH4MgPO4 6H2O NH MgPO H O (NH4MgPO4∙6H2O slowrelease slow release andor or wastewaters salts sense characterization 95 9 5 9. MgCl26H2O MgClHO MgCl2 MgCl MgCl2∙6H2O MgSO47H2O MgSOHO MgSO4 7H2O MgSO MgSO4∙7H2O MgO MgCO3. MgCO3 MgCO . (MgCO3) preacidification, preacidification pre acidification, acidification pre-acidification lowcost low cost 90 respectively 1 L1 L L- crystals 46ꟷ56% 46ꟷ56 ꟷ (46ꟷ56 97 formed Xray X ray precipitates NHMgPO NH4MgPO HO (MgCO3 46ꟷ5 (46ꟷ5 (MgCO 46ꟷ (46ꟷ

RESUMO: Objetivou-se avaliar a eficácia do sulfato de magnésio e cetamina em reduzir o requerimento de propofol, remifentanil e o resgate analgésico pós-operatório de gatas submetidas à ovariohisterectomia eletiva. Trinta gatas foram pré-medicadas com acepromazina (0,05 mg/kg) e morfina (0,3 mg/kg), intramuscular, e induzidas a inconsciência com propofol para intubação orotraqueal. As infusões contínuas (IC) de propofol e remifentanil foram iniciadas e os animais foram aleatoriamente alocados em três grupos: grupo sulfato de magnésio (MG) que recebeu bolus (50 mg/kg) e IC (80 mg/kg) de sulfato de magnésio; grupo cetamina (KG) que recebeu bolus (0,5 mg/kg) e IC (1,8 mg/kg/h) de cetamina; grupo controle (CG) que recebeu bolus e IC de solução salina 0,9%. As funções cardiovasculares e respiratórias, o tempo de extubação e a pontuação de resgate pós-operatório foram registrados e descritos com nível de significância de 95% (P < 0.05). O tempo de infusão dos tratamentos foi de 21,5 ± 3,4 e 21,0 ± 2,4 minutos no KG e MG, respectivamente (P = 0.194). As taxas de infusões de remifentanil (P = 0.336) e propofol (P = 0.716) foram similares entre grupos. Na análise de dor pós-operatória as escalas não demonstraram diferenças entre grupos quanto a número de resgates, pontuação de resgate ou tempo para o primeiro resgate. Em conclusão, os protocolos propostos foram seguros e efetivos. Contudo, o sulfato de magnésio e cetamina não demonstraram analgesia pós-operatória adicional ou efeitos adjuvantes anestésicos significativos. RESUMO Objetivouse Objetivou se pósoperatório pós operatório eletiva prémedicadas pré medicadas 0,05 005 0 05 (0,0 mg/kg mgkg mg kg 0,3 03 3 (0, mg/kg, , intramuscular orotraqueal (IC MG (MG 50 (5 80 (8 (KG 0,5 5 1,8 18 1 8 (1, mg/kg/h mgkgh h CG (CG 09 9 0,9% respiratórias 95 P 0.05. 0.05 . 0.05) 215 21 21, 34 4 3, 210 24 2 2, 0.194. 0194 0.194 194 0.194) 0.336 0336 336 0.716 0716 716 pósoperatória operatória resgates conclusão efetivos Contudo significativos 0,0 00 0, (0 ( 1, (1 0,9 0.0 019 0.19 19 0.33 033 33 0.71 071 71 0. 01 0.1 0.3 0.7 07 7

ABSTRACT: This study assessed the efficacy of magnesium sulfate and ketamine hydrochloride in reducing the demand for propofol, remifentanil, and postoperative rescue analgesia in cats undergoing elective ovariohysterectomy. Thirty cats were premedicated with acepromazine (0.05 mg/kg) and morphine (0.3 mg/kg) intramuscularly and induced to unconsciousness with propofol for orotracheal intubation. The continuous infusion (CI) of propofol and remifentanil were started and animals and were randomly allocated into three groups: the magnesium sulfate group (MG) received one bolus (50 mg/kg) and CI (80 mg/kg/h) of magnesium sulfate; the ketamine group (KG) received bolus (0.5 mg/kg) and CI (1.8 mg/kg/h) of ketamine hydrochloride; the control group (CG) received bolus and CI of 0.9% saline solution. Cardiovascular and respiratory functions, extubation time, and rescue postoperative scores were assessed and data were described with a significance level of 95% (P < 0.05). The infusion period of treatments was 21.5 ± 3.4 and 21.0 ± 2.4 minutes in the KG and MG, respectively (P = 0.194). The infusion rates of remifentanil (P = 0.336) and propofol (P = 0.716) were similar between groups. Analysis of the postoperative pain scales revealed no significant intergroup differences in rescue frequency, rescue score, and time to the first rescue analgesia. In conclusion, the proposed protocols were safe and effective, yet it is noteworthy that both magnesium sulfate and ketamine failed to demonstrate significant additional postoperative analgesic or adjuvant anesthetic effects. ABSTRACT ovariohysterectomy 0.05 005 0 05 (0.0 mg/kg mgkg mg kg 0.3 03 3 (0. intubation (CI groups MG (MG 50 (5 80 (8 mg/kg/h mgkgh h (KG 0.5 5 1.8 18 1 8 (1. CG (CG 09 9 0.9 solution functions 95 P 0.05. . 0.05) 215 21 21. 34 4 3. 210 24 2 2. 0.194. 0194 0.194 194 0.194) 0.336 0336 336 0.716 0716 716 frequency score conclusion effective effects 0.0 00 0. (0 ( 1. (1 019 0.19 19 0.33 033 33 0.71 071 71 01 0.1 0.7 07 7

In the present study a spectrophotometric method for Cr(VI) determination in organic fertilizers, especially those from tanning industry residues, is proposed. Conditions for chromium extraction, extract clean-up and analytical characteristics of the method were established. The method is based on the complexation of Cr(VI) with 1,5-diphenylcarbazide (DPC) in acid medium (pH 2.0). A mixture of NaOH and Na2CO3 solution at 0.125 and 0.07 mol L–1 (pH 12), respectively, and heating at 90 °C for 60 min were the best conditions for chromium extraction. Florisil and activated charcoal were tested for clean-up of the extract, with activated charcoal being effective. Under the established conditions, the calibration linear range is up to 2500 μg L–1 Cr(VI), the results obtained are in agreement with the value of a certified reference material (CRM041), precision is better than 5% for five consecutive determinations of a solution at 1000 μg L–1 of Cr(VI) and the limit of quantification is 1.62 μg g–1. In can be concluded that the method is robust, accurate and precise, and can be easily applied for the determination of Cr(VI) in routine analysis, since it complies with legislation of most countries regarding the maximum allowed concentration of 2 μg g–1 of Cr(VI). CrVI Cr VI Cr(VI fertilizers residues proposed extraction cleanup clean 1,5diphenylcarbazide 15diphenylcarbazide diphenylcarbazide 1,5 1 5 DPC (DPC pH 2.0. 20 2.0 . 0 2.0) NaCO Na CO Na2CO 0125 125 0.12 007 07 0.0 L1 L L– 12, 12 , 12) respectively 9 C 6 effective 250 CrVI, CRM041, CRM041 CRM (CRM041) 100 162 62 1.6 g1 g robust precise analysis g– CrVI. 5diphenylcarbazide 15 1, 2. 012 0.1 00 0. 25 CRM04 (CRM041 10 16 1. 01 CRM0 (CRM04 (CRM0 (CRM

This paper elucidates the inseparable connection between the pursuit of a more ecologically sustainable society and the quest for socioeconomic justice. It also demonstrates why Unconditional Basic Income (UBI) is an effective policy to act on both fronts. First, the corresponding theory on environmental and socioeconomic oppression sheds light on the argument that both types of domination stem from the same historical process and are inherently interconnected. Addressing one without considering the other is essentially flawed; they are both features and consequences of present society. Acknowledging the historical debt owed to vulnerable economic classes and developing countries is imperative. Green republicanism could potentially establish a theoretical foundation for social-ecological thinking. Defining freedom as non-domination and applying this concept to nature are essential prerequisites for overcoming socioeconomic and environmental oppression. UBI is presented and discussed theoretically as a strong solution to address these two challenges. It serves not only as a means to facilitate the transition to a post-productivist society, transforming labor relations, but also as a catalyst for the development of circular economies and more sustainable occupations. Additionally, the basic income policy implemented in the city of Maricá, Brazil, is cited as empirical evidence showcasing the environmental and socioeconomic values of UBI. justice (UBI fronts First interconnected flawed imperative socialecological social ecological thinking nondomination non challenges postproductivist post productivist relations occupations Additionally Maricá Brazil

This study presents a solution to solid waste problems, focusing on spent lithium-ion batteries (LiBs) and iron ore tailings (IOT) from the Mariana environmental accident in Brazil. The approach involves the production CoFe2O4 from LiBs and IOT, which serves as a catalyst for solar photo-Fenton reactions for methylene blue (MB) decolorization and as an electrochemical sensor for ascorbic acid (AA) detection. Chemical analysis showed recycling potential, with 45.22 ± 0.22% m m−1 Co from LiBs and 14.9 ± 1.5% m m−1 Fe from IOT, determined by inductively coupled plasma atomic emission spectroscopy (ICP OES) and flame atomic absorption spectrometry (FAAS). The sol-gel synthesized CoFe2O4 exhibited a crystallite size of 51.9 ± 1.3 nm and agglomerated crystal clusters. Recycled-CoFe2O4 exhibited a 98.1% MB decolorization efficiency in 60 min under solar irradiation and remained above 92.3% in all 7 reuse cycles. The electrochemical sensor exhibited a coefficient of determination of 0.9987, a sensitivity of 3.352 ± 0.0428 μA mol L−1, and a limit of detection of 0.5511 µM in the concentration range of 1.96 to 23.08 mmol L−1 for AA detection. This study demonstrates the potential of recycled-CoFe2O4 in an environmentally friendly dye removal and as an electrochemical sensor, offering sustainable waste management and resource utilization with solar energy. problems lithiumion lithium ion (LiBs IOT (IOT Brazil CoFeO CoFe O CoFe2O photoFenton photo Fenton (MB (AA 4522 45 22 45.2 022 0 0.22 m1 1 m− 149 14 9 14. 15 5 1.5 ICP OES FAAS. FAAS . (FAAS) solgel sol gel 519 51 51. 13 3 1. clusters RecycledCoFe2O4 RecycledCoFeO Recycled Recycled-CoFe2O 981 98 98.1 6 923 92 92.3 cycles 09987 9987 0.9987 3352 352 3.35 00428 0428 0.042 L1 L 05511 5511 0.551 196 96 1.9 2308 23 08 23.0 L− recycledCoFe2O4 recycledCoFeO recycled recycled-CoFe2O energy 452 4 2 45. 02 0.2 (FAAS RecycledCoFe RecycledCoFe2O 98. 92. 0998 998 0.998 335 35 3.3 0042 042 0.04 0551 551 0.55 19 230 23. recycledCoFe recycledCoFe2O 0. 099 99 0.99 33 3. 004 04 0.0 055 55 0.5 09 0.9 00 05

This research aims to develop a precise and efficient dispersive solid-phase microextraction (DSPE) technique using third-generation polyamidoamine (PAMAM) dendrimer-grafted nanoparticles to quantify benzoylurea pesticides in green tea, black tea, and oolong tea infusions. The extraction efficiency is optimized through single-factor adjustments of key parameters, including adsorbent quantity (5-20 mg), adsorption duration (5-20 min), desorbent identity (methanol, acetonitrile), volume (100-600 μL), sodium chloride concentration (0-10%, m/v), and sample solution pH (3-8). The optimized method demonstrates linearity in the range of 2-500 μg L-1, with limits of detection (LODs) ranging from 0.6-1.5 μg L-1 and limits of quantification (LOQs) from 2.0 5.0 μg L-1. Recovery rates of 81.2-96.0% are achieved, with intra-day relative standard deviations (RSDs) of 1.4-2.8% and inter-day relative standard deviations of 2.0-3.9%, indicating high accuracy and repeatability. The successful application of detecting residues in commercial tea samples underscores the strong potential of the technique to determine benzoylurea analyte levels. solidphase solid phase DSPE (DSPE thirdgeneration third generation PAMAM (PAMAM dendrimergrafted dendrimer grafted infusions singlefactor single factor parameters 520 5 20 (5-2 mg, mg , mg) min, min min) methanol, methanol (methanol acetonitrile, acetonitrile acetonitrile) 100600 100 600 (100-60 μL, μL μL) 010%, 010 0 10%, 10 (0-10% m/v, mv m/v m v m/v) 38. 38 3 8 . (3-8) 2500 2 500 2-50 L1, L1 L 1, 1 LODs (LODs 0.61.5 0615 0.6 1.5 6 0.6-1. L- LOQs (LOQs 2. 50 5. L1. 1. 81.296.0% 812960 81.2 96.0% 81 96 81.2-96.0 achieved intraday intra day RSDs (RSDs 1.42.8% 1428 1.4 2.8% 4 1.4-2.8 interday inter 2.03.9%, 2039 3.9%, 9 2.0-3.9% repeatability levels 52 (5- 10060 60 (100-6 010% 01 10% (0-10 (3-8 250 2-5 61 0.61. 061 06 0. 15 0.6-1 296 81.296.0 81296 812 81. 960 96.0 81.2-96. 42 1.42.8 142 14 28 2.8 1.4-2. 03 2.03.9% 203 39 3.9% 2.0-3.9 (5 1006 (100- (0-1 (3- 25 2- 0.61 0.6- 29 81.296. 8129 96. 81.2-96 1.42. 1.4-2 2.03.9 3.9 2.0-3. ( (100 (0- (3 81.296 81.2-9 1.42 1.4- 2.03. 3. 2.0-3 (10 (0 81.29 81.2- 2.03 2.0- (1

Sensor calibration for dissolved gas is a critical and necessary step to ensure consistent sensor response over time and under different conditions. In this work, we describe a 3D printed device that facilitates the calibration of gas sensors. The device effectively maintained gas concentration in the solution for at least 2 h. Analytical curves were constructed in the pH range of 2 to 12, yielding determination coefficients surpassing 0.98. The chosen method proved suitable for the calibration of the sensors. Furthermore, using accurate and reliable reference sensors contributed to obtaining precise and trustworthy measurements. conditions work D h 12 098 0 98 0.98 Furthermore measurements 1 09 9 0.9 0.

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 (