Navegando por Autor "Teodoro, Filipe Simões"
Agora exibindo 1 - 14 de 14
Resultados por página
Opções de Ordenação
Item Adsorção de metais e corantes em celulose modificada com anidrido trimelítico.(2015) Teodoro, Filipe Simões; Gurgel, Leandro Vinícius Alves; Mageste, Aparecida Barbosa; Santos, Igor José Boggione; Gil, Laurent FrédéricA contaminação de corpos d’água por efluentes industriais é um problema ambiental crescente que necessita de atenção, não só frente à crise hídrica vivida pelo país, mas também, pela preservação deste bem para as próximas gerações. Dois poluentes importantes presentes nestes efluentes são os metais pesados e os corantes têxteis. Estes poluentes são tóxicos para várias formas de vida e não biodegradáveis, tendem a acumular-se em organismos causando várias doenças e desordens. Dessa forma a remoção destes poluentes dos efluentes industriais se mostra uma preocupação importante. A bioadsorção é um processo de tratamento de águas residuais que tem atraído considerável interesse recentemente na remoção deste tipo de contaminante. Neste trabalho foi preparado um adsorvente a partir da celulose para ser utilizado na remoção de metais tóxicos e corantes de soluções idealmente contaminadas em batelada. A celulose foi modificada quimicamente utilizando o anidrido trimelítico (AT), produzindo um material contendo funções ácido carboxílico em sua estrutura (CAT). A esterificação da celulose (C) foi investigada e otimizada considerando o efeito da quantidade de AT e o tempo de reação além da análise da porcentagem de ganho de massa (pgm) e do número de funções ácidas (nCOOH) introduzidas. As modificações na celulose foram avaliadas pelas técnicas de FTIR, TGA, RMN 13C, PCZ, MEV e análise elementar de C, H e N. Estudos de adsorção em batelada foram realizados empregando os metais cobalto (II), cobre(II) e níquel(II) e os corantes safranina-T e auramina-O. A CAT apresentou capacidade de adsorção máxima (Qmáx) de 0,960, 1,487 e 1,014 mmol.g-1 para Co+2, Cu+2 e Ni+2 e 3,743 e 5,175 mmol.g-1 para safranina-T e auramina-O, respectivamente. Foram avaliados a influência da dosagem de adsorvente, do pH, do tempo de contato e da concentração inicial de adsorvato. Para tentar descrever os sistemas de adsorção foram utilizados os modelos de isoterma de Langmuir, Freundlich, Sips, Redlich- Peterson, Hill-de Boer, Fowler-Guggenheim, um modelo para multicamadas e os modelos cinéticos de pseudo primeira e pseudo segunda ordem. Estudos de dessorção e re-adsorção mostraram a potencialidade de reutilização do adsorvente CAT. Os parâmetros termodinâmicos de adsorção ΔadsH° e ΔadsS° foram determinados com o auxílio da calorimetria de titulação isotérmica (ITC) que juntamente com a energia livre padrão ΔadsG° foram utilizados para discutir o mecanismo de adsorção de metais em CAT.Item Aminated cellulose as a versatile adsorbent for batch removal of As(V) and Cu(II) from mono- and multicomponent aqueous solutions.(2020) Pereira, Amanda Raimundi; Soares, Liliane Catone; Teodoro, Filipe Simões; Carvalho, Megg Madonyk Cota Elias; Ferreira, Gabriel Max Dias; Savedra, Ranylson Marcello Leal; Savedra, Melissa Fabíola Siqueira; Martineau Corcos, Charlotte; Silva, Luis Henrique Mendes da; Prim, Damien; Gurgel, Leandro Vinícius AlvesA bioadsorbent (CEDA) capable of adsorbing As(V) and Cu(II) simultaneously was prepared by tosylation of microcrystalline cellulose (MC) and nucleophilic substitution of the tosyl group by ethylenediamine. MC, tosyl cellulose, and CEDA were characterized by elemental C, H, N, and S analysis, infrared spectroscopy, and 13C solid-state nuclear magnetic resonance spectroscopy. The adsorption of As(V) and Cu (II) on CEDA was evaluated as a function of solution pH, contact time, and initial solute concentration. The maximum adsorption capacities of CEDA for As(V) and Cu(II) were 1.62 and 1.09 mmol g1 , respectively. The interactions of As(V) and Cu(II) with CEDA were elucidated using thermodynamic parameters, molecular quantum mechanics calculations, and experiments with ion exchange of Cd(II) by Cu(II), and As(V) by SO4 2. Adsorption enthalpies were determined as a function of surface coverage of the CEDA, using isothermal titration calorimetry, with DadsH values of 32.24 ± 0.07 and 93 ± 2 kJ mol1 obtained for As(V) and Cu(II), respectively. The potential to reuse CEDA was evaluated and the interference of other ions in the adsorption of As(V) and Cu(II) was investigated. Multi-component experiments showed that Cd(II), Co(II), Ni(II), and Pb(II) did not interfere in the adsorption of Cu(II), while SO4 2 inhibited As(V) adsorption.Item Application of a new carboxylate-functionalized sugarcane bagasse for adsorptive removal of crystal violet from aqueous solution : kinetic, equilibrium and thermodynamic studies.(2015) Ferreira, Bruno Christiano Silva; Teodoro, Filipe Simões; Mageste, Aparecida Barbosa; Gil, Laurent Frédéric; Freitas, Rossimiriam Pereira de; Gurgel, Leandro Vinícius AlvesA new carboxylate-functionalized sugarcane bagasse (SMA) was prepared via a solvent-free procedure involving esterification of sugarcane bagasse with Meldrum’s acid. The optimized conditions provided SMA with a percent weight gain of 86.0% and 4.69±0.20 mmol/g of carboxylic acid groups. SMA was characterized by FTIR, TGA, elemental analysis and SEM. Kinetic experiments showed that the amount of crystal violet adsorbed increased with increasing temperature and equilibrium was reached at 12 h. Adsorption kinetics followed a pseudo-second-order model. The Arrhenius and Eyring models were used to obtain the activation energy and changes in free energy, enthalpy, and entropy of activation for the adsorption process. The calculated activation energy (14.14 kJ/mol) suggested physical adsorption of CV onto SMA. The equilibrium data were well fitted to the Langmuir and Sips isotherms. Maximum adsorption capacity was 692.1 mg/g at 45 ◦C. Thermodynamic parameters such as changes in free energy, enthalpy and entropy were also determined.Item Application of pyridine-modified chitosan derivative for simultaneous adsorption of Cu(II) and oxyanions of Cr(VI) from aqueous solution.(2021) Gonçalves, Fernanda Jorge; Gurgel, Leandro Vinícius Alves; Soares, Liliane Catone; Teodoro, Filipe Simões; Ferreira, Guilherme Max Dias; Coelho, Yara Luiza; Silva, Luis Henrique Mendes da; Prim, Damien; Gil, Laurent FrédéricThe bioadsorbent C1, which is a chitosan derivative prepared in a one-step synthesis, was successfully used to adsorb Cr(VI) and Cu(II) simultaneously. Here, for the first time the simultaneous adsorption of a cation and an anion was modeled using the Corsel model for kinetics and the Real Adsorbed Solution Theory model for equilibrium data. Batch studies of the adsorption of Cu(II) and Cr(VI) in single and binary aqueous solutions were performed as a function of initial solute concentration, contact time, and solution pH. The maximum adsorption capacities of C1 in single and binary aqueous solutions were 1.84 and 1.13 mmol g− 1 for Cu(II) and 3.86 and 0.98 mmol g− 1 for Cr(VI), respectively. The reuse of C1 was investigated, with Cu(II) ions being almost completely desorbed and fully re-adsorbed. For Cr(VI), the desorption was incomplete resulting in a lower re- adsorption. Energy-dispersive X-ray spectroscopy was used for mapping the distributions of Cr(VI) and Cu(II) adsorbed on the C1 surface in single and binary adsorption systems. Isothermal titration calorimetry experiments were performed for Cr(VI) and Cu(II) adsorption in single solutions. The thermodynamic parameters of adsorption showed that the adsorption of both metal ions was enthalpically driven, but entropically unfavorable.Item Application of raw and chemically modified biomasses for heterogeneous Cu-catalysed conversion of aryl boronic acids to phenols derivatives.(2022) Torres, Fernanda Guimarães; Teodoro, Filipe Simões; Gurgel, Leandro Vinícius Alves; Bourdreux, Flavien; Zayene, Olfa; Gaucher, Anne; Gil, Laurent Frédéric; Prim, DamienThis work describes the application of raw and chemically modified cellulose and sug- arcane bagasse for ipso-hydroxylation of aryl boronic acids in environmentally friendly reaction conditions. The catalytic efficiency of five support-[Cu] materials was compared in forming phenols from aryl boronic acids. Our investigation highlights that the CEDA-[Cu] material (6-deoxy-6- aminoethyleneamino cellulose loaded with Cu) leads to the best results under very mild reaction conditions. The optimized catalytic sequence, allowing a facile transformation of boronic acids to phenols, required the mandatory and joint presence of the support, Cu2O, and KOH at room temperature. CEDA-[Cu] was characterized using 13C solid-state NMR, ICP, and FTIR. The use of CEDA-[Cu] accounts for the efficacious synthesis of variously substituted phenol derivatives and presents very good recyclability after five catalytic cycles.Item Batch and continuous adsorption of Cu(II) and Zn(II) ions from aqueous solution on bi‐functionalized sugarcane‐based biosorbent.(2022) Teodoro, Filipe Simões; Soares, Liliane Catone; Filgueiras, Jefferson Gonçalves; Azevedo, Eduardo Ribeiro de; Patino Agudelo, Alvaro Javier; Herrera Adarme, Oscar Fernando; Silva, Luis Henrique Mendes da; Gurgel, Leandro Vinícius AlvesA new one-pot synthesis method optimized by a 23 experimental design was developed to prepare a biosorbent, sugarcane bagasse cellulose succinate pyromellitate (SBSPy), for the removal of Cu(II) and Zn(II) from single-component aqueous solutions, in batch and continuous modes. The bi-functionalization of the biosorbent with ligands of diferent chemical structures increased its selectivity, improving its performance for removing pollutants from contaminated water. The suc- cinate moiety favored Cu(II) adsorption, while the pyromellitate moiety favored Zn(II) adsorption. Sugarcane bagasse (SB) and SBSPy were characterized using several techniques. Analysis by 13C Multi-CP SS NMR and FTIR revealed the best order of addition of each anhydride that maximized the chemical modifcation of SB. The maximum adsorption capacities of SBSPy for Cu(II) and Zn(II), in batch mode, were 1.19 and 0.95 mmol g-1, respectively. Homogeneous surface difusion, intraparticle difusion, and Boyd models were used to determine the steps involved in the adsorption process. Isothermal titration calorimetry was used to assess changes in enthalpy of adsorption as a function of SBSPy surface coverage. Fixed- bed column adsorption of Cu(II) and Zn(II) was performed in three cycles, showing that SBSPy has potential to be used in water treatment. Breakthrough curves were well ftted by the Thomas and Bohart-Adams models.Item Modeling mono- and multi-component adsorption of cobalt(II), copper(II), and nickel(II) metal ions from aqueous solution onto a new carboxylated sugarcane bagasse. Part I: Batch adsorption study.(2015) Ramos, Stela Nhandeyara do Carmo; Xavier, Amália Luísa Pedrosa; Teodoro, Filipe Simões; Carvalho, Megg Madonyk Cota Elias; Gonçalves, Fernanda Jorge; Gil, Laurent Frédéric; Freitas, Rossimiriam Pereira de; Gurgel, Leandro Vinícius AlvesA new carboxylated-functionalized sugarcane bagasse (STA) was prepared through the esterification of sugarcane bagasse with trimellitic anhydride. The optimized synthesis conditions yield STA with a percent weight gain of 73.9% and the number of carboxylic acid groups accounted for 3.78 mmol/g. STA was characterized by FTIR, elemental analysis, TGA, PZC, and SEM. Adsorption kinetics followed a pseudosecond- order model. The adsorption rate constant showed the following order: k2,Ni 2+ > k2,Cu 2+ > k2,Co 2+. Four mono- and multi-component isotherm models were used to model the adsorption systems. Monocomponent experimental data were fitted to Langmuir and Sips models; whereas, multicomponent data were fitted to modified extended Langmuir and P-factor models. The maximum adsorption capacities (Qmax,mono) obtained from the Langmuir model were 1.140, 1.197, and 1.563 mmol/g for Co2+, Cu2+, and Ni2+, respectively. The competitive studies demonstrated that the multicomponent adsorption capacity (Qmax,multi) was smaller than Qmax,mono, as a result of the interaction between the metal ions. Desorption studies showed that all metal ions could be fully desorbed from STA.Item New use for succinylated sugarcane bagasse containing adsorbed Cu2+ and Ni2+ : efficient catalysts for gas-phase n-hexane and n-heptane oxidation reactions.(2017) Balzer, Rosana; Probst, Luiz Fernando Dias; Fajardo, Humberto Vieira; Teodoro, Filipe Simões; Gurgel, Leandro Vinícius Alves; Gil, Laurent FrédéricThis study describes the use of succinylated twice-mercerized sugarcane bagasse containing adsorbed Cu2+ or Ni2+ ions from spiked aqueous solutions (2MSBA-Cu and 2MSBA-Ni) as heterogeneous catalysts for the catalytic oxidation of n-hexane and n-heptane in gas phase. To the best of our knowledge, this is the first study in which a spent adsorbent material based on lignocellulose biomass is used in the catalytic oxidation of volatile organic compounds. The adsorbent and spent adsorbent materials were characterized by FTIR, TGA and XRD. The amount of Cu2+ and Ni2+ adsorbed on 2MSBA was 0.49 and 2.49 mmol g−1, respectively. The catalysts were active for total oxidation of n-hexane and n-heptane, even at low temperatures. 2MSBA-Cu exhibited higher catalytic activity than 2MSBA-Ni and surprisingly their performances were comparable or superior to those of some catalysts reported in the literature, including noble metal-based catalysts.Item Removal of cobalt (II), copper (II), and nickel (II) ions from aqueoussolutions using phthalate - functionalized sugarcane bagasse : mono - and multicomponent adsorption in batch mode.(2016) Ramos, Stela Nhandeyara do Carmo; Xavier, Pedrosa; Teodoro, Filipe Simões; Gil, Laurent Frédéric; Gurgel, Leandro Vinícius AlvesThis study describes, in detail, the chemical modification of sugarcane bagasse with phthalic anhydrideto produce a carboxylate-functionalized sugarcane bagasse (SPA). The optimized modification condi-tions yielded SPA with a percent weight gain of 77.08% and an amount of carboxylic acid groups of 4.76mmol/g. The SPA was characterized by PZC, FTIR, elemental analysis, TGA, and SEM-EDX. An SPA adsor-bent was used to remove Co2+, Cu2+, and Ni2+from aqueous solution in mono- and multicomponentsystems in batch mode. The adsorption kinetics followed a pseudo-second-order model. The adsorptionrate constants assumed the following order: k2,Co2+> k2,Ni2+> k2,Cu2+. Four mono- and multicomponentisotherm models were used to model the adsorption data. Monocomponent data were well described bythe Langmuir model, whereas bicomponent data were well described by the modified extended Lang-muir and P-Factor models. The maximum adsorption capacities (Qmax,mono) for the Langmuir model were0.561, 0.935, and 0.932 mmol/g for Co2+, Cu2+, and Ni2+, respectively. Adsorption in bicomponent systemsrevealed that Cu2+suppressed the adsorption of Co2+and Ni2+, whereas Ni2+suppressed the adsorptionof Co2+. Desorption studies revealed that the SPA adsorbent could be fully desorbed with a 1 mol/L HNO3solution.Item Synthesis and application of a new carboxylated cellulose derivative. Part I : removal of Co2+, Cu2+ and Ni2+ from monocomponent spiked aqueous solution.(2016) Teodoro, Filipe Simões; Ramos, Stela Nhandeyara do Carmo; Carvalho, Megg Madonyk Cota Elias; Mageste, Aparecida Barbosa; Ferreira, Gabriel Max Dias; Silva, Luis Henrique Mendes da; Gil, Laurent Frédéric; Gurgel, Leandro Vinícius AlvesA new carboxylated cellulose derivative (CTA) was prepared from the esterification of cellulose with 1,2, 4-Benzenetricarboxylic anhydride. CTA was characterized by percent weight gain (pwg), amount of carboxylic acid groups (nCOOH), elemental analysis, FTIR, TGA, solid-state 13C NMR, X-ray diffraction (DRX), specific surface area, pore size distribution, SEM and EDX. The best CTA synthesis condition yielded a pwg and nCOOH of 94.5% and 6.81 mmol g 1, respectively. CTA was used as an adsorbent material to remove Co2+, Cu2+ and Ni2+ from monocomponent spiked aqueous solution. Adsorption studies were developed as a function of the solution pH, contact time and initial adsorbate concentration. Langmuir model better fitted the experimental adsorption data and the maximum adsorption capacities estimated by this model were 0.749, 1.487 and 1.001 mmol g 1 for Co2+, Cu2+ and Ni2+, respectively. The adsorption mechanism was investigated by using isothermal titration calorimetry. The values of DadsH were in the range from 5.36 to 8.09 kJ mol 1, suggesting that the mechanism controlling the phenomenon is physisorption. Desorption and re-adsorption studies were also performed. Desorption and re-adsorption efficiencies were closer to 100%, allowing the recovery of both metal ions and CTA adsorbent.Item Synthesis and application of a new carboxylated cellulose derivative. Part II : removal of Co2+, Cu2+ and Ni2+ from bicomponent spiked aqueous solution.(2017) Teodoro, Filipe Simões; Herrera Adarme, Oscar Fernando; Gil, Laurent Frédéric; Gurgel, Leandro Vinícius AlvesIn the second part of this series of studies, the competitive adsorption of three binary systems Cu2+–Co2+, Cu2+–Ni2+ and Co2+–Ni2+ on a carboxylated cellulose derivative (CTA) was evaluated in binary equimolar (1:1) metal–ion aqueous solutions. Bicomponent adsorption studies were developed as a function of contact time and initial metal ion concentration. Bicomponent adsorption kinetic data was modeled by monocomponent kinetic models of pseudo-first- (PFO) and pseudo-second-order (PSO) and a competitive kinetic model of Corsel. Bicomponent adsorption isotherm data was modeled by the ideal adsorbed solution theory (IAST) and real adsorbed solution theory (RAST) models. The monocomponent isotherm models implemented into the IAST were the Langmuir and Sips models, whereas for the RAST model only the Langmuir model was implemented because this model provided the best prediction of the bicomponent isotherm data. The surface of the CTA adsorbent after bicomponent adsorption of metal ions was also examined by SEM-EDX. The effect of one metal ion on the adsorption capacity of another metal ion was discussed in detail with basis on the kinetic and thermodynamics parameters. The selectivity and performance of the CTA adsorbent for the removal of Cu2+, Co2+ and Ni2+ was also evaluated and discussed.Item Synthesis and application of a new carboxylated cellulose derivative. Part III : removal of auramine-O and safranin-T from mono- and bi-component spiked aqueous solutions.(2018) Teodoro, Filipe Simões; Carvalho, Megg Madonyk Cota Elias; Ferreira, Gabriel Max Dias; Herrera Adarme, Oscar Fernando; Savedra, Ranylson Marcello Leal; Savedra, Melissa Fabíola Siqueira; Silva, Luis Henrique Mendes da; Gil, Laurent Frédéric; Gurgel, Leandro Vinícius AlvesIn the third part of this series of studies, the adsorption of the basic textile dyes auramine-O (AO) and safranin-T (ST) on a carboxylated cellulose derivative (CTA) were evaluated in mono- and bi-component spiked aqueous solutions. Adsorption studies were developed as a function of solution pH, contact time, and initial dye concentration. Adsorption kinetic data were modeled by monocomponent kinetic models of pseudo-first- (PFO), pseudo-second-order (PSO), intraparticle diffusion, and Boyd, while the competitive kinetic model of Corsel was used to model bicomponent kinetic data. Monocomponent adsorption equilibrium data were modeled by the Langmuir, Sips, Fowler-Guggenhein, Hill de-Boer, and Konda models, while the IAST and RAST models were used to model bicomponent equilibrium data. Monocomponent maximum adsorption capacities for AO and ST at pH 4.5 were 2.841 and 3.691 mmol g−1, and at pH 7.0 were 5.443 and 4.074 mmol g−1, respectively. Bicomponent maximum adsorption capacities for AO and ST at pH 7.0 were 1.230 and 3.728 mmol g−1. Adsorption enthalpy changes (ΔadsH) were obtained using isothermal titration calorimetry. The values of ΔadsH ranged from −18.83 to −5.60 kJ mol−1, suggesting that physisorption controlled the adsorption process. Desorption and re-adsorption of CTA was also evaluated.Item Trimellitated sugarcane bagasse : a versatile adsorbent for removal of cationic dyes from aqueous solution. Part I : batch adsorption in a monocomponent system.(2018) Fideles, Renata Aparecida; Ferreira, Gabriel Max Dias; Teodoro, Filipe Simões; Herrera Adarme, Oscar Fernando; Silva, Luis Henrique Mendes da; Gil, Laurent Frédéric; Gurgel, Leandro Vinícius AlvesTrimellitated-sugarcane bagasse (STA) was used as an environmentally friendly adsorbent for removal of the basic dyes auramine-O (AO) and safranin-T (ST) from aqueous solutions at pH 4.5 and 7.0. Dye adsorption was evaluated as a function of STA dosage, agitation speed, solution pH, contact time, and initial dye concentration. Pseudo-first- and pseudo-second-order, Elovich, intraparticle diffusion, and Boyd models were used to model adsorption kinetics. Langmuir, Dubinin-Radushkevich, Redlich-Peterson, Sips, Hill-de Boer, and Fowler-Guggenheim models were used to model adsorption isotherms, while a Scatchard plot was used to evaluate the existence of different adsorption sites. Maximum adsorption capacities for removal of AO and ST were 1.005 and 0.638 mmol g 1 at pH 4.5, and 1.734 and 1.230 mmol g 1 at pH 7.0, respectively. Adsorption enthalpy changes obtained by isothermal titration energy and entropy of adsorption were calculated. These thermodynamic parameters were also used to evaluate the adsorption mechanism at both pH values.Item Trimellitated sugarcane bagasse : a versatile adsorbent for removal of cationic dyes from aqueous solution. Part II: batch and continuous adsorption in a bicomponent system.(2019) Fideles, Renata Aparecida; Teodoro, Filipe Simões; Xavier, Amália Luísa Pedrosa; Herrera Adarme, Oscar Fernando; Gil, Laurent Frédéric; Gurgel, Leandro Vinícius AlvesIn the second part of this series of studies, the bicomponent adsorption of safranin-T (ST) and auramine-O (AO) on trimellitated sugarcane bagasse (STA) was evaluated using equimolar dye aqueous solutions at two pH values. Bicomponent batch adsorption was investigated as a function of contact time, solution pH and initial concentration of dyes. Bicomponent kinetic data were fitted by the pseudo-first-order and pseudo-second-order models and the competitive model of Corsel. Bicomponent equilibrium data were fitted by the real adsorbed solution theory model. The antagonistic interactions between ST and AO in the adsorption systems studied contributed to obtain values of maximum adsorption capacity in mono- (Qmax,mono) and bicomponent (Qmax,multi) lower than unity (Qmax,multi/Qmax,mono at pH 4.5 for ST of 0.75 and AO of 0.37 and at pH 7 for ST of 0.94 and AO of 0.43). Mono- and bicomponent adsorption of dyes in a fixed-bed column was evaluated at pH 4.5. The breakthrough curves were fitted by the Thomas and Bohart-Adams original models. Desorption of ST in a fixed-bed column was studied. The results obtained from the bicomponent batch and continuous adsorption showed that the presence of ST most affected the AO adsorption than the presence of AO affected the ST adsorption.