Print version ISSN 1516-1439
Mat. Res. vol.16 no.1 São Carlos Jan./Feb. 2013 Epub Nov 02, 2012
Surface cellulose modification with 2-aminomethylpyridine for copper, cobalt, nickel and zinc removal from aqueous solution
Edson Cavalcanti Silva FilhoI*; Luiz Sousa Santos JúniorI; Marcia Maria Fernandes SilvaI; Maria Gardênnia FonsecaII; Sirlane Aparecida Abreu SantanaIII; Claudio AiroldiIV
IInterdisciplinary Laboratory for Advanced Materials LIMAV, Federal University of Piauí UFPI, CEP 64049-550, Teresina, PI, Brazil. *E-mail: email@example.com
IIChemistry Department, Federal University of Paraíba UFPI, CEP 58059-900, João Pessoa, PB, Brazil
IIIChemistry Department, Federal University of Maranhão UFMA, CEP 65080-540, São Luiz, MA, Brazil
IVInstitute of Chemistry, University of Campinas UNICAMP, P. O. Box 6154, CEP 13084-971, Campinas, SP, Brazil
Cellulose was first modified with thionyl chloride, followed by reaction with 2-aminomethylpyridine to yield 6-(2'-aminomethylpyridine)-6-deoxycellulose. The resulting chemically-immobilized surface was characterized by elemental analysis, FTIR, 13C NMR and thermogravimetry. From 0.28% of nitrogen incorporated in the polysaccharide backbone, the amount of 0.10 ± 0.01 mmol of the proposed molecule was anchored per gram of the chemically modified cellulose. The available basic nitrogen centers attached to the covalent pendant chain bonded to the biopolymer skeleton were investigated for copper, cobalt, nickel and zinc adsorption from aqueous solution at room temperature. The newly synthesized biopolymer gave maximum sorption capacities of 0.100 ± 0.012, 0.093 ± 0.021, 0.074 ± 0.011 and 0.071 ± 0.019 mmol.g1 for copper, cobalt, nickel and zinc cations, respectively, using the batchwise method, whose data was fitted to different sorption models, the best fit being obtained with the Langmuir model. The results suggested the use of this anchored biopolymer for cation removal from the environment.
Keywords: cellulose, modification, 2-aminometylpyridine, sorption, cations
The field of surface chemistry describes a variety of natural or synthetic materials suitable for chemical surface reactions, with the main objective to improve the overall capacity for applications1,2. A lot of these supports are derived from inorganic compounds, such as silica and other oxides, however, some important reports describe excellent results in which are related to biopolymers3-5. In this sense, the most abundant biopolymer is cellulose, but, the effectiveness of its applications is associated with new synthesized polymers after chemical surface modifications, by incorporating desired molecules that possess functional groups, which are, in general, Lewis basic sites, with the investigations normally focused on sorption processes6-8. One of the most known synthetic methods is based on preparing, in the first step, a halogen derivative9, by including it on the original polymeric structure at carbon 6, as shown in Figure 1.
Biopolymer halogenation is preferred due to the fact that chlorine is the most effective halogen, whose preferential sequence is given as follows: chlorine > bromine > iodine > fluorine. Then, the effectiveness of such reaction routes has been explored by using different chemicals as precursors, with the objective of transferring this element to the cellulosic polymeric chain. A series of other reactants are available for such process, but thionyl chloride is the most effective and, consequently, is the most used10, followed by phosphoryl oxychloride11, N-chlorosuccinimide12 and tosyl chloride13.
The next step of the chemical modification occurs by nucleophilic attack, which is provided by organic molecules embracing basic centers to act as chelating agents in the corresponding structure, such as nitrogen, sulfur, oxygen and/or phosphorous atoms. As mentioned before, these Lewis bases present great efficiency for aqueous metal ion removal6-8. However, functional basic groups attached to the pendant chains have also been employed for other important applications9,14-18.
Oxidation is another systematic process to incorporate organic moieties containing functional groups in this fantastic biopolymer that can be performed through esterification and also etherification reactions. In the first case, the reaction usually takes places on carbons 2 and 3, unlike halogenation that occurs preferentially at carbon 6, and it is also used as an intermediate step for the incorporation of other functional groups. However, both chemical processes follow the same route as halogenations, through reaction on carbon 6, with greatest advantage being the occurrence of only one step19. The molecule chosen to be immobilized has a chlorine atom that will react with the hydroxyl group, releasing hydrochloric acid to form the ether or ester bonds20. Besides, acylation has also been widely investigated as a cellulose surface modification reaction, starting from a cyclic organic in which all three structural hydroxyl groups are involved. In this case, the nucleophilic agents attack the carbonyl group of the strained anhydrides to yield ester bonds, being the most important advantage the absence of halogens in the final structure, without releasing hydrochloric acid21-23.
In recent years, the use of the materials based on Green Chemistry principles has been widely investigated in order to reduce the emission of pollutants from the synthetic procedures, as solvents and co-products. Thus, some investigations have already demonstrated solvent-free syntheses are desirable and the amount of organic groups immobilized under these conditions has increased6,7,21-25.
Regarding the application of natural or synthetic materials, many pristine or chemically modified polymeric compounds have been extensively applied for cation removal from aqueous solutions and these processes can provide large amounts of metal ion retention or ion exchange processes. In this context, a lot of investigated materials with excellent sorption properties are those on synthetic mesoporous silicas and silica gel supports26-28, chemically modified phyllosilicates29-31, chitosan, as obtained and after modification with a series of pendant chains24,32,33, synthetic phosphates34,35, chemically modified celluloses6-8,21-23 and others36-38. These inorganic or biopolymer materials research fields are continuously expanding, however, the biopolymers, and specially cellulose, have a huge advantage, since they are quite abundant in nature, renewable, biodegradable and easily obtained at low cost.
The simple presence of metals as extra components in nature, in a variety of forms, has encouraged finding solutions for this problem, especially when they are discharged directly to soil or to ground water. Domestic, industrial and agricultural residues are pollutant sources, which can reach not only potable water, but also the alimentary chain, affecting the entire ecosystem. In addition, the toxicity of a variety of metals in aquatic organisms has awakened and focused biological interest. Based on this unfavorable condition, efforts are focused to sorb trace metals using natural materials that can perform an important role in these species determinations in aqueous systems. Therefore, these concerns are part of an organized society that is worried about the welfare of the community and any material is welcome to apply for such applications1,6. Although sorption is the most frequently used method, due to its low cost and possible support reuse, among other factors, other methods have been used for cation removal from aquatic environments, such as ion exchange39,40, electrodeposition41,42, precipitation43,44, coagulation and flocculation45,46, among others.
The present investigation deals with chemically modified cellulose, after incorporating the 2-aminomethylpyridine moiety as a pendant functional chain, which is covalently bound to the polymeric framework. These attached nitrogen atoms in the pendant chains are potential sites to bond cations from aqueous solution in a heterogeneous system, whose interactive processes are followed at the solid/liquid interface.
Material and methods
Materials and apparatus
Cellulose (Merck), thionyl chloride (Chemika), N,N'-dimethylformamide (Synth), ammonium hydroxide (Aldrich) and 2-aminomethylpyridine (Aldrich) were used as received. Cation solutions were prepared from reagent grade nitrates (Vetec).
The amount of 2-aminomethylpyridine pendant chains anchored onto the cellulose surface was calculated based on the percent of nitrogen, determined through elemental analysis on a Perkin Elmer, model 2400, elemental analyzer. The infrared spectra of the samples were obtained in KBr pellets by accumulating 32 scans on a Bomem spectrophotometer, MB-series, in the 4000-400 cm1 range with 4 cm1 resolution. Solid state nuclear magnetic resonance spectra of the samples for carbon were obtained on a Bruker AC 300/P spectrometer at room temperature. For each run, approximately one gram of each solid sample was compacted into a 7 mm zirconium oxide rotor. The measurements were obtained at 75.47 MHz frequencies with a magic angle spinning of 4 kHz. In order to increase the signal to noise ratio the CP/MAS technique was used, with pulse repetition of 2 s and contact times of 1 and 2 ms, respectively. The thermogravimetric curves in an argon atmosphere were obtained on a TA instrument, coupled to a thermobalance, model 1090 B, using a heating rate of 0.167 K.s1, with a flow of 30 cm3.s1, varying from room temperature to 1273 K, with an initial mass of approximately 10 mg of solid sample. The amount of cation sorbed was determined by the difference between the initial concentration in the aqueous solution and that found in the supernatant, by using an ICP OES Perkin Elmer 3000 DV apparatus. For each experimental point, the repetivity was checked by at least one duplicate run.
Preparation of modified biopolymer
For chlorodeoxycellulose synthesis, 10.0 g of cellulose (Cel), previously activated at 353 K for 12 hours, was suspended in 200 cm3 of N,N-dimethylformamide (DMF), followed by the slow addition of 35.0 cm3 of thionyl chloride (SOCl2) at 353 K, under mechanical stirring. After ending the addition, stirring was continued at the same temperature for another 4 hours. From this reaction the cellulose chloride obtained was washed with several portions of dilute ammonium hydroxide solution and the supernatant in each operation was eliminated to return to neutral pH. To complete the washing, the suspension was exhaustively treated with distilled water. The solid was then filtered and dried under vacuum at room temperature9, giving 6-chlorodeoxycellulose (CelCl). Then, 1.0 g of this synthesized chlorinated biopolymer was reacted with 14.6 cm3 of 2-aminomethylpyridine (amp) under reflux and with mechanical stirring for 4 hours, followed by filtration, using a sintered glass filter. The new solid obtained (Celamp) was dried in vacuum at room temperature for 24 hours8.
The capacity of the chemically modified cellulose to sorb cations from aqueous solution, in deionized water with pH near to 6, was determined in duplicate runs, using a batch process with divalent copper, cobalt, nickel and zinc, by using a mass (m) of about 30 mg of Celamp suspended in 25.0 cm3 of an aqueous solution with concentrations of each metal varying from 0.10 to 5.0 mmol.dm3. These suspensions were mechanically stirred for 4 hours at room temperature and separated by centrifugation for 10 minutes. The supernatants were pipetted and the cations were determined by ICP OES. The sorption capacities (Nf) were calculated by considering: Nf = (ni ns).m1, where ni and ns are the number of moles in the initial and supernatant solutions25.
The sorption at the solid/liquid interface demands a competition between the solvent (solv) bonded to the anchored surface (AS) that is gradually displaced by the solute in solution to reach equilibrium:
To determine the maximum capacity, Ns, the experimental data related to the number of moles in the supernatant for each point, Cs, and the Nf obtained were fitted to a modified Langmuir equation, with b being a constant associated with the chemical equilibrium at the solid/liquid interface47.
The Freundlich equation used to obtain the sorption parameters48 is given by the expression:
where nf represents the reactivity of energetic sites of the biomaterial and Kf is a constant related to the chemical equilibrium at the solid/liquid interface. Another procedure applied to this same equilibrium was the Temkin model49, in which Nf is calculated:
As observed, the three classic overall isotherm models are normally applied for sorption surface equilibria, with the solute under study most often measured with batchwise procedures. The amount sorbed is plotted as a function of the remaining solute concentration. Thus, the evaluation of the isotherm parameters is clearly obtained by the coefficient of determination, which value indicates the goodness of the fit between the data and the chosen isotherm.
The data obtained for solute/surface interaction in this heterogeneous system can be interpreted through the models: i) the Langmuir model assumes that similar energy of sorption sites are gradually saturated in a monolayer behavior, ii) the Freundlich model establishes the same sorption process that occurs in a multilayer condition and iii) the Temkin model admits both possibilities in solute sorbing on the surface at the same time.
In the present case, the sorption models were compared through three statistical methods. The first considers the correlation coefficient (r) obtained by means of linear regression of each equation, with a scaling factor derived by the division of each individual deviation with the standard deviation of the corresponding variable, data which was calculated in a specific program.
Results and discussion
The cellulose chemically modified with 2-aminomethylpyridine gave from nitrogen elemental analysis, a value of 0.28 + 0.02% that corresponds to the degree of immobilization of 0.10 + 0.10 mmol of this element per gram of cellulose. Based on chlorine elemental analysis a significant reduction of the amount of chlorine in the preceding chlorated precursor was observed from 17.58 to 8.61%. This reduced value is due to the molar mass of aminopyridine incorporated on the biopolymer, which result shows cellulose functionalization. The incorporated amount was low when compared to other matrices, but within the expected value, when the same molecule was immobilized, for example, onto silica-chloropropyl, it presented close results50. This fact can be explained by the steric hindrance caused by the hydrophobicity of this molecule.
The infrared spectra of the crude cellulose and the modified biopolymers are shown in Figure 2. Typical wavenumbers for hydroxyl groups for Cel, such as -CH-OH and -CH2-OH stretching in the 3300 to 3400 cm1 interval, are shown in Figure 2a. The methylene group stretchings from the incorporated molecule are located at 2900 cm1 and the band in the 3000 to 2800 cm1 range is attributed to the presence of -C-H groups, since both -CH and -CH2 group ratio for cellulose is in a 5:1 proportion6,51,52. The OH bending vibrations for the cellulose surface are located at 1639 cm1, which differs from primary and secondary hydroxyl bending that appears in the 1500 to 1200 cm1 interval, and the C-O stretching vibration6,51,52 is observed at 1100 cm1.
The appearance of two new bands at 709 and 752 cm1 for chlorinated cellulose, as shown in Figure 2b, correspond to the C-Cl stretching vibration from the branched part of the original polymer. The displacement and decreasing size of the band originally observed in the cellulose at 894 cm1, as shown in Figure 2a, is shifted to 865 cm1 for the CelCl compound. The spectrum of 2-aminopyridine chemically modified cellulose is shown in Figure 2c, in which a decrease of n(C-Cl) vibration confirmed the effectiveness of the reaction. The vibrations related to aliphatic and aromatic C-H did not present significant visualization, due to the overlapping bands. In the 1670 to 1720 cm1 interval an intense band appeared associated with the axial CC deformation of the monosubstituted aromatic ring, as well as also to the angular N-H deformation that is observed in the 1650 to 1600 cm1 range. The other bands were little affected by the reaction, as previously observed6,51,52.
Nuclear magnetic resonance spectrum in the solid state for the carbon nucleus of pure cellulose is presented in Figure 3a. A set of five distinct peaks are present: C1 at 104 ppm, C4 at 88 ppm, C2, C3, and C5 at 74 ppm, and C6 at 65 ppm. For CelCl several changes in the chemical shifts for C4 and mainly for C6 are observed, which are presented at 82 and 44 ppm, respectively, as shown in Figure 3b. For Celam biopolymer, whose spectrum is shown in Figure 3c, a very weak peak in the 170 to 160 ppm interval appeared, due to low immobilized amount anchored, that refers to C8, in agreement with the low amount immobilized. The presence of a new signal at 65 ppm is also observed that corresponds to the methylene group C7 of the immobilized molecule, but better visualized than C8. The other carbons, C9 to C12, are not shown, they should appear in the 120 to 150 ppm interval, however, the experimental signal collections were not efficient to demonstrate significant peaks50,52,53.
The Celam sample, presented a low crystallinity, with characteristics near to the amorphous form, as shown in the diffractogram in Figure 4b, showing microcrystaline cellulose, with the appearance of peaks in the same region. Thus, as could be observed, the chlorinated cellulose presented a crystallographic profile distinct from microcrystalline cellulose9 and the final diffractogram gave close profile to that of the microcrystalline form, as shown in Figure 4a.
The thermogravimetric curves for cellulose and the chemically modified celluloses are shown in Figure 5. For cellulose only one thermal event is observed in the decomposition process in the 536 to 647 K range, as shown in Figure 5a, with a mass loss of 92%. The chlorinated biopolymer, as shown in Figure 5b, gave a mass loss in the 386 to 430 K interval, which correlated to the water physically sorbed onto the surface. The second step, with mass loss of 23%, between 438 and 534 K, corresponds to the displacement of hydrochloric acid, with the condensation of hydroxyl groups on carbons 2 and 3. The last event in this process, from 521 K, can be interpreted as cellulose fiber decomposition. The immobilized biopolymer Celam, as shown in Figure 5c, has a behavior close to the other chemically modified celluloses6,8,22, with the same observed events, to give the degradation order: Celam < CelCl < Cel54.
The sorption isotherms for divalent copper, cobalt, nickel and zinc for cellulose chemically modified with 2-aminopyridine are shown in Figure 6. As observed, the sorption order was the same as for cellulose containing ethylenediamine plus acetylacetone8, for this biopolymer chemically modified with butyldiamine7 and for other anchored materials50,55,56, having maximum sorption values of: 0.100 ± 0.012, 0.093 ± 0.021, 0.074 ± 0.011 and 0.071 ± 0.019 mmol.g1 for Cu2+, Co2+, Ni2+ and Zn2+, respectively.
The basic centers ratio available in matrix (B) and the corresponding sorbed amount (M/B) are listed in Table 1. In the present biopolymer the M/B ratio reached a value very close to one cation for two basic centers in the complexation process, indicating that the pendant chain acted as a bidentate chelating agent. This biopolymer in the present way of complexation used the total capacity of the available centers for copper and demonstrated also to be selective for cobalt. A proposed scheme of metal complexation is shown in Figure 7, in which the available basic nitrogen centers coordinate the cations, with the charge being counterbalanced by the counter anions.
The results obtained from the Langmuir, the Freundlich and the Temkim sorption models for these divalent cations with Celam are listed in Table 2 and the new isotherms obtained from the adjusted fit models are shown in Figure 8.
These data show that copper followed by cobalt were the cations with higher sorptions, however, for all cations excellent linear coefficients were obtained when adjusted to the Langmuir model, being values higher than 0.99. The fit for the Freundlich and the Temkin models gave lower values, which indicated that the isotherms are not well‑adjusted to these models. The data obtained for solute/surface interaction in this heterogeneous system assumes that similar energy of sorption sites are gradually saturated in a monolayer behavior, to give the good linear fit of experimental data to the Langmuir model. From these results the number of moles for the monolayer proposed by the Langmuir model is close to maximum capacity of sorption. In this condition the sites involved in the sorption process are the basic groups available, which are saturated, especially by copper and in any case, the cations are complexed in a bidentate form, as shown in Figure 7. By comparing the experimental isotherms with one obtained from theoretical calculations, based on the studied models, the results corroborate with the data listed in Table 2, with a better fit to the proposed Langmuir model.
The sorption isotherms, mainly for copper and cobalt, shown in Figure 6, are adjusted to the 2 L type of the Langmuir model, following the Giles classification, with a depression concavity, that is, with a slope to reach the plateau, whose behavior is an unequivocal representation of the formed monolayer57. These interactions can be interpreted as cation transfer from solution to basic centers attached to the pendant chains, through the complexation by the amino groups at the solid/liquid interface.
The investigation associated with cation removal from aqueous solutions based on the sorption process through metal species complexation, with chemically modified matrices, is of extreme environmental importance as established by Green Chemistry principles58, mainly when chemically modified surfaces are presented as efficient for this purpose. These removals from aqueous solution are promising for a series of cations.
A successful incorporation of the 2-aminomethylpyridine molecule in the absence of solvent onto cellulose is confirmed. Based on elemental analysis, the biopolymer Celam gave a percentage of nitrogen that opposed to the decrease amount of chlorine, after the incorporation of 2-aminomethylpyridine. This result is unequivocal evidence that an effective immobilization of such molecule took place on the cellulose surface. An expressive support for this immobilization is given by the axial C=C band related to the aromatic ring in infrared spectroscopy, followed by its chemical shift at 160 ppm from 13C NMR, the change in crystallinity and also by the decomposition profile of the biopolymer.
The anchored biopolymer Celam presented a good capacity in cation removal from aqueous solutions, to give the maximum sorptions of: 0.100, 0.093, 0.074 and 0.071 mmol.g1 in the order Cu2+ > Co2+ > Ni2+ > Zn2+, demonstrating efficiency in complexing cations with a ratio near to 2:1, for basic center attached to the pendant chain/cation ratio.
The linearity obtained for the Langmuir fit for the data was higher than other models. As observed, the data shwoed that chemically modified cellulose has higher capacity than the original biopolymer for interacting with cations in solutions, which property can be used in applications in order to reduce the toxic effects of metals in the environment.
The authors are indebted to FAPESP and CNPq for financial support and fellowships.
Babel S and Kurniawan TA. Low-cost adsorbents for heavy metals uptake from contaminated water: a review. Journal of Hazardous Materials. 2003; 97:219-243. http://dx.doi.org/10.1016/S0304-3894(02)00263-7 [ Links ]
Haensch C, Hoeppener S and Schubert US. Chemical modification of self-assembled silane based monolayers by surface reactions. Chemical Society Reviews. 2010; 39:2323‑2334. PMid:20424728. http://dx.doi.org/10.1039/b920491a [ Links ]
Klemm D, Heublein B, Fink HP and Bohn A. Cellulose: fascinating biopolymer and sustainable raw material. Angewandte Chemie International Edition. 2005; 44:3358‑3393. PMid:15861454. http://dx.doi.org/10.1002/anie.200460587 [ Links ]
Moon RJ, Martini A, Nairn J, Simonsen J and Youngblood J. Cellulose nanomaterials review: structure, properties and nanocomposites. Affiliation Information 1. School of Mechanical Engineering,Purdue University, West Lafayette, USA. Chemical Society Review. 2011; 40:3941-3994. PMid:21566801. http://dx.doi.org/10.1039/c0cs00108b [ Links ]
Silva Filho EC, Melo JCP and Airoldi C. Preparation of ethylenediamine-anchored cellulose and determination of thermochemical data for the interaction between cations and basic centers at the solid/liquid interface. Carbohydrate Research. 2006; 341:2842-2850. PMid:17022956. http://dx.doi.org/10.1016/j.carres.2006.09.004 [ Links ]
Silva Filho EC, Melo JCP, Fonseca MG and Airoldi C. Cation removal using cellulose chemically modified by a Schiff base procedure applying green principles. Journal of Colloid and Interface Science. 2009; 340:8-15. PMid:19748100. http://dx.doi.org/10.1016/j.jcis.2009.08.012 [ Links ]
Silva Filho EC, Silva LS, Lima LCB, Santos Júnior LS, Santos MRMC, Matos JME et al. Thermodynamic data of 6-(4 -aminobutylamino)-6-deoxycellulose sorbent for cation removal from aqueous solutions. Separation Science and Technology. 2011; 46:2566-2574. http://dx.doi.org/10.1080/01496395.2011.599826 [ Links ]
Silva Filho EC, Santana SAA, Melo JCP, Oliveira FJVE and Airoldi C. X-ray diffraction and thermogravimetry data of cellulose, chlorodeoxycellulose and aminodeoxycellulose. Journal of Thermal Analysis and Calorimetry. 2010; 100:315‑321. http://dx.doi.org/10.1007/s10973-009-0270-6 [ Links ]
Tashiro T and Shimura Y. Removal of mercuric ions by systems based on cellulose derivatives. Journal of Applied Polymer Science. 1982; 27:747-756. http://dx.doi.org/10.1002/app.1982.070270235 [ Links ]
Castro GR, Alcântara IL, Roldan PS, Bozano DF, Padilha PM, Florentino AO et al. Synthesis, characterization and determination of the metal ions adsorption capacity of cellulose modified with p-aminobenzoic groups. Materials Research. 2004; 7:329-334. http://dx.doi.org/10.1590/S1516‑14392004000200018 [ Links ]
Furuhata KI, Aoki N, Suzuki S, Arai N, Sakamoto M, Saegusa Y et al. Reaction of dichloroallose units in a chlorodeoxycellulose with lithium chloride under homogeneous conditions in N,N-dimethylacetamide. Carbohydrate Research. 1994; 258:169‑178. http://dx.doi.org/10.1016/0008‑6215(94)84083-0 [ Links ]
Jalali N, Moztarzadeh F, Mozafari M, Asgari S, Motevalian M and Alhosseini SN. Surface modification of poly(lactide‑co‑glycolide) nanoparticles by d-a‑tocopheryl polyethylene glycol 1000 succinate as potential carrier for the delivery of drugs to the brain. Colloids and Surfaces A. 2011; 392:335-342. http://dx.doi.org/10.1016/j.colsurfa.2011.10.012 [ Links ]
Asouhidou DD, Triantafyllidis KS, Lazaridis NK and Matis KA. Adsorption of Remazol Red 3BS from aqueous solutions using APTES- and cyclodextrin-modified HMS-type mesoporous silicas. Colloids and Surface A. 2009; 346:83-90. http://dx.doi.org/10.1016/j.colsurfa.2009.05.029 [ Links ]
Silva ALP, Sousa KS, Germano AFS, Oliveira VV, Espínola JGP, Fonseca MG et al. A new organofunctionalized silica containing thioglycolic acid incorporated for divalent cations removal - a thermodyamic cation/basic center interaction. Colloids and Surface A. 2009; 332:144-149. http://dx.doi.org/10.1016/j.colsurfa.2008.09.010 [ Links ]
Khan A, Badshah S and Airoldi C. Biosorption of some toxic metal ions by chitosan modified with glycidylmethacrylate and diethylenetriamine. Chemical Engineering Journal. 2011; 171:159-166. http://dx.doi.org/10.1016/j.cej.2011.03.081 [ Links ]
Khan A, Badshah S and Airoldi C. Dithiocarbamated chitosan as a potent biopolymer for toxic cation remediation. Colloids and Surface B. 2011; 87:88-95. PMid:21652182. http://dx.doi.org/10.1016/j.colsurfb.2011.05.006 [ Links ]
O'Conell DW, Birkinshaw C and O'Dwyer TF. Heavy metals adsorbents prepared from the modification of cellulose: a review. Bioresource Technology. 2008; 99:6709-6724. PMid:18334292. http://dx.doi.org/10.1016/j.biortech.2008.01.036 [ Links ]
Ratanakamnuan U, Atong D and Aht-Ong D. Cellulose esters from waste cotton fabric via conventional and microwave heating. Carbohydrate Polymers. 2012; 87:84-94. http://dx.doi.org/10.1016/j.carbpol.2011.07.016 [ Links ]
Melo JCP, Silva Filho EC, Santana SAA and Airoldi C. Maleic anhydride incorporated onto cellulose and thermodynamics of cation-exchange process at the solid/liquid interface. Colloids and Surface A. 2009; 346:138-145. http://dx.doi.org/10.1016/j.colsurfa.2009.06.006 [ Links ]
Melo JCP, Silva Filho EC, Santana SAA and Airoldi C. Synthesized cellulose/succinic anhydride as an ion exchanger. Calorimetry of divalent cations in aqueous suspension. Thermochimica Acta. 2011; 524:29-34. http://dx.doi.org/10.1016/j.tca.2011.06.007 [ Links ]
Melo JCP, Silva Filho EC, Santana SAA and Airoldi C. Exploring the favorable ion-exchange ability of phthalylated cellulose biopolymer using thermodynamic data. Carbohydrate Research. 2010; 345:1914-1921. PMid:20673881. http://dx.doi.org/10.1016/j.carres.2010.06.012 [ Links ]
Sousa KS, Silva Filho EC and Airoldi C. Ethylenesulfide as a useful agent for incorporation into the biopolymer chitosan in a solvent-free reaction for use in cation removal. Carbohydrate Research. 2009; 344:1716-1723. PMid:19560124. http://dx.doi.org/10.1016/j.carres.2009.05.028 [ Links ]
Santana SAA, Vieira AP, Silva Filho EC, Melo JCP and Airoldi C. Immobilization of ethylenesulfide on babassu coconut epicarp and mesocarp for divalent cation sorption. Journal of Hazardous Materials. 2010; 174:714-719. PMid:19836886. http://dx.doi.org/10.1016/j.jhazmat.2009.09.109 [ Links ]
Arakaki LNH, Alves APM, Silva Filho EC, Fonseca MG, Oliveira SF, Espínola JGP et al. Sequestration of Cu(II), Ni(II), and Co(II) by ethyleneimine immobilized on silica. Thermochimica Acta. 2007; 453:72-74. http://dx.doi.org/10.1016/j.tca.2006.10.016 [ Links ]
Arakaki LNH, Fonseca MG, Silva Filho EC, Alves APM, Sousa KS and Silva ALP. Extraction of Pb(II), Cd(II), and Hg(II) from aqueous solution by nitrogen and thiol functionality grafted to silica gel measured by calorimetry. Thermochimica Acta. 2006; 450:12-15. http://dx.doi.org/10.1016/j.tca.2006.06.012 [ Links ]
Oliveira FJVE, Silva Filho EC, Melo Junior MA and Airoldi C. Modified coupling agents based on thiourea, immobilized onto silica. Thermodynamics of copper adsorption. Surface Science. 2009; 603:2200-2206. http://dx.doi.org/10.1016/j.susc.2009.04.020 [ Links ]
Fonseca MG, Silva Filho EC, Machado Junior RSA, Arakaki LNH, Espínola JGP and Airoldi C. Zinc phyllosilicates containing amino pendant groups. Journal of Solid State Chemistry. 2004; 177:2316-2322. http://dx.doi.org/10.1016/j.jssc.2004.02.026 [ Links ]
Morais CC, Silva Filho EC, Silva OG, Fonseca MG, Arakaki LNH and Espínola JGP. Thermal characterization of modified phyllosilicates with aromatic heterocyclic amines. Journal of Thermal Analysis and Calorimetry. 2007; 87:767-770. http://dx.doi.org/10.1007/s10973-006-7854-1 [ Links ]
Lee YC, Kim EJ, Yang JW and Shin HJ. Removal of malachite green by adsorption and precipitation using aminopropyl functionalized magnesium phyllosilicate. Journal of Hazardous Materials. 2011; 192:62-70. PMid:21616589. [ Links ]
Machado MO, Lopes ECN, Sousa KS and Airoldi C. The effectiveness of the protected amino group on crosslinked chitosans for copper removal and the thermodynamics of interaction at the solid/liquid interface. Carbohydrate Research. 2009; 77:760-766. [ Links ]
Fan L, Luo C, Lv Z, Lu F and Qiu H. Preparation of magnetic modified chitosan and adsorption of Zn2+ from aqueous solutions. Colloids and Surface B. 2011; 88:574‑581. PMid:21868204. http://dx.doi.org/10.1016/j.colsurfb.2011.07.038 [ Links ]
Silva OG, Fonseca MG and Arakaki LNH. Silylated calcium phosphates and their new behavior for copper retention from aqueous solution. Colloids and Surface A. 2007; 301:376-381. http://dx.doi.org/10.1016/j.colsurfa.2006.12.072 [ Links ]
Silva OG, Silva Filho EC, Fonseca MG, Arakaki LNH and Airoldi C. Hydroxyapatite organofunctionalized with silylating agents for heavy cation removal. Journal of Colloid and Interface Science. 2006; 302:485-491. PMid:16904683. http://dx.doi.org/10.1016/j.jcis.2006.07.010 [ Links ]
Daković A, Kragović M, Rottinghaus GE, Sekulić , Milićević S, Milonjić SK et al. Influence of natural zeolitic tuff and organozeolites surface charge on sorption of ionizable fumonisin B1. Colloids and Surface B. 2010; 76:272-278. PMid:20004084. http://dx.doi.org/10.1016/j.colsurfb.2009.11.003 [ Links ]
Awwad NS, Gad HMH, Ahmad MI and Aly HF. Sorption of lanthanum and erbium from aqueous solution by activated carbon prepared from rice husk. Colloids and Surface B. 2010; 81:593-599. PMid:20800456. http://dx.doi.org/10.1016/j.colsurfb.2010.08.002 [ Links ]
Aochi YO and Farmer WJ. Effects of surface charge and particle morphology on the sorption/desorption behavior of water on clay minerals. Colloids and Surface A. 2011; 374:22-32. http://dx.doi.org/10.1016/j.colsurfa.2010.10.039 [ Links ]
Silva MLCP, Silva GLJP and Villela Filho DN. Hydrous tantalum phosphates for ion exchange purposes. A systematic study. Materials Research. 2002; 5:71-75. http://dx.doi.org/10.1590/S1516-14392002000100012 [ Links ]
Biskup B and Subotic B. Kinetic analysis of the exchange process between sodium ions from zeolite A and cadmium, copper and nickel ions from solutions. Separation and Purification Technology. 2004; 37;17-31. http://dx.doi.org/10.1016/S1383-5866(03)00220-X [ Links ]
Chen P-Y. The assessment of removing strontium and cesium cation from aqueous solution based on the combined methods of ionic liquid extraction and electrodeposition. Electrochimica Acta. 2007; 52:5484-5492. http://dx.doi.org/10.1016/j.electacta.2007.03.010 [ Links ]
Mokone TP, Lewis AE and van Hille RP. Effect of post‑precipitation of colloidal metal sulphide precipitates. Hydrometallurgy. 2012; 119-120:55-66. http://dx.doi.org/10.1016/j.hydromet.2012.02.015 [ Links ]
Mokone TP, van Hille RP and Lewis AE. Effect of solution chemistry on particle characteristics during metal sulfide precipitation. Journal of Colloid and Interface Science. 2012; 351:10-18. PMid:20705300. http://dx.doi.org/10.1016/j.jcis.2010.06.027 [ Links ]
Al-Abri M, Dakheel A, Tizaoui C and Hilal N. Combined humic substance and heavy metals coagulation, and membrane filtration under saline conditions. Desalination. 2010; 253:46‑50. http://dx.doi.org/10.1016/j.desal.2009.11.037 [ Links ]
Henneberr YK, Kraus TEC, Fleck JA, Krabbenhoft DP, Bachand PM and Horwath WR. Removal of inorganic mercury and methylmercury from surface waters following coagulation of dissolved organic matter with metal-based salts. Science of the Total Environmental. 2011; 409:631-637. PMid:21075424. http://dx.doi.org/10.1016/j.scitotenv.2010.10.030 [ Links ]
Langmuir IJ. The constitution and fundamental properties of solids and liquids, Part 1. Solids. Journal of the American Chemical Society. 1916; 38:2221-2295. http://dx.doi.org/10.1021/ja02268a002 [ Links ]
Freundlich HMF. Über die adsorption in Lösungen. Physics Chemistry. 1906; 57A:385-470. [ Links ]
Temkin MJ and Pyzhev V. Recent modification to Langmuir isotherms. Acta Physics URSS. 1940; 12:217-225. [ Links ]
Sales JAA, Faria FP, Prado AGS and Airoldi C. Attachment of 2-aminomethylpyridine molecule onto grafted silica gel surface and its ability in chelating cations. Polyhedron. 2004; 23:719-725. http://dx.doi.org/10.1016/j.poly.2003.11.051 [ Links ]
Oh SY, Yoo DI, Shin Y and Seo G. FTIR analysis of cellulose treated with sodium hydroxide and carbon dioxide. Carbohydrate Research. 2005; 340:417-428. PMid:15680597. http://dx.doi.org/10.1016/j.carres.2004.11.027 [ Links ]
Pavia DL, Basser GM and Morrill TC. Introduction to Spectroscopy. 2nd ed. Saunder: College Publishing, New York; 1996. [ Links ]
Kono H, Yunoki S, Shikano T and Fujiwara T. CP/MAS 13C NMR study of cellulose and cellulose derivatives. 1. Complete assignment of the CP/MAS 13C NMR spectrum of the native cellulose. Journal of the American Chemical Society. 2002; 124:506-7511. PMid:12071760. http://dx.doi.org/10.1021/ja010704o [ Links ]
Airoldi C and Arakaki LNH. Immobilization of ethylenesulfide on silica surface through sol-gel process and some thermodynamic data of divalent cation interactions. Polyhedron. 2001; 20:929-936. http://dx.doi.org/10.1016/S0277-5387(01)00743-4 [ Links ]
Giles CH, Macewan TH, Nakhwa SN and Smith DJ. Studies in adsorption. XI. A system of classification of solution adsorption isotherms. Journal of the Chemical Society. 1960; 1:3973‑3993. http://dx.doi.org/10.1039/jr9600003973 [ Links ]
Received: May 25, 2012
Revised: July 24, 2012