Synthesis of polyamidoxime chelating ligand from polymer‐grafted corn‐cob cellulose for metal extraction

A conventional free‐radical initiating process was used to prepare graft copolymers from acrylonitrile (AN) with corn‐cob cellulose with ceric ammonium nitrate (CAN) as an initiator. The optimum grafting was achieved with corn‐cob cellulose (anhydroglucose unit, AGU), mineral acid (H₂SO₄), CAN, and AN at concentrations of 0.133, 0.081, 0.0145, and 1.056 mol/L, respectively. Furthermore, the nitrile functional groups of the grafted copolymers were converted to amidoxime ligands with hydroxylamine under basic conditions of pH 11 with 4 h of stirring at 70°C. The purified acrylic polymer‐grafted cellulose and polyamidoxime ligand were characterized by Fourier transform infrared spectroscopy and field emission scanning electron microscopy analysis. The ligand showed an excellent copper binding capacity (4.14 mmol/g) with a faster rate of adsorption (average exchange rate = 7 min), and it showed a good adsorption capacity for other metal ions as well. The metal‐ion adsorption capacities of the ligand were pH‐dependent in the following order: Cu²⁺ > Co²⁺ > Mn²⁺ > Cr³⁺ > Fe³⁺ > Zn²⁺ > Ni²⁺. The metal‐ion removal efficiency was very high; up to 99% was removed from the aqueous media at a low concentration. These new polymeric chelating ligands could be used to remove aforementioned toxic metal ions from industrial wastewater. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40833.     

Removal of concentrated heavy metal ions from aqueous solutions using polymers with enriched amidoxime groups

Particulate and fibrous adsorbents with enriched amidoxime groups were synthesized by using a novel monomer N,N′‐dipropionitrile acrylamide. The adsorption properties of amidoximated poly(N,N′‐dipropionitrile acrylamide) [poly(DPAAm)] particles and a nonwoven fabric grafted with the same for UO₂²⁺, Pb²⁺, Cu²⁺, and Co²⁺ at high concentrations were investigated by batch process. Metal ion adsorption studies were conducted from metal ion solutions with different initial concentrations (100–1500 ppm). It was shown that particulated amidoximated poly(DPAAm) has higher adsorption capacity than amidoximated nonwoven fabrics for all metal ions, especially for uranyl ions. The results of the adsorption studies showed that the interaction between UO₂²⁺ and amidoximated groups agree with the Langmuir‐type isotherm. From the Langmuir equation, the adsorption capacities were found as 400 mg UO₂²⁺/g dry amidoximated poly(DPAAm) and 250 mg UO₂²⁺/g dry amidoximated graft polymer. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1705–1710, 2004     

Stability constants of amidoximated chitosan‐g‐poly(acrylonitrile) copolymer for heavy metal ions

Amidoximated chitosan‐g‐poly(acrylonitrile) (PAN) copolymer was prepared by a reaction between hydroxylamine and cyano group in chitosan‐g‐PAN copolymer prepared by grafting PAN onto crosslinked chitosan with epychlorohydrine. The adsorption and desorption capacities for heavy metal ions were measured under various conditions. The adsorption capacity of amidoximated chitosan‐g‐PAN copolymer increased with increasing pH values, and was increased for Cu²⁺ and Pb²⁺ but a little decreased for Zn²⁺ and Cd²⁺ with increasing PAN grafting percentage in amidoximated chitosan‐g‐PAN copolymer. In addition, desorption capacity for all metal ions was increased with increasing pH values in contrast to the adsorption results. Stability constants of amidoximated chitosan‐g‐PAN copolymer were higher for Cu²⁺ and Pb²⁺ but lower for Zn²⁺ and Cd²⁺ than those of crosslinked chitosan. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 469–476, 1999     

Introduction of amidoxime groups into cellulose and its ability to adsorb metal ions

Introduction of amidoxime groups into cellulose substrate was investigated by reaction of cyano-group-containing celluloses such as cyanoethylcellulose (CE-Cell) and acrylonitrilegrafted cellulose (G-Cell) with hydroxylamine at 70°C in water medium (pH = 7.0). Dissolving pulp from softwood was used as the cellulose sample, and photografting was applied to the preparation of G-Cell, where hydrogen peroxide was used as a photoinitiator. Degree of substitution (DS) of CE-Cell and percent grafting of G-Cell employed were less than 1.5 and 40, respectively. The amidoximation of CE-Cell proceeded easily, and the amidoxime content increased with increasing the reaction time and increasing the concentration of hydroxylamine, but the amidoxime content of G-Cell decreased significantly at longer reaction time. The amidoximated samples prepared by CE-Cell exhibited an ability to adsorb metal ions such as Cu²⁺, Ni²⁺, and Co²⁺, and the adsorbed amount of Cu²⁺ was highest among the three metal ions. Moreover, the adsorption of Cu²⁺ varied depending on the DS of CE-Cell. That is, the absorption ability was reduced when the sample was prepared using CE-Cell with higher DS. The amidoximated samples prepared from G-Cell showed adsorption of Cu²⁺ similar to samples prepared by CE-Cell with lower DS, irrespective of percent grafting. © 1995 John Wiley & Sons, Inc.     

Amidoximation of acrylonitrile radiation‐grafted onto low‐density polyethylene and its physicochemical characterization

Membranes were prepared by the direct radiation grafting of acrylonitrile onto low‐density polyethylene films. These grafted membranes were amidoximated using hydroxylamine hydrochloride in basic medium. The influence of monomer concentration and swelling behaviour of grafted membrane, amidoximated grafted membrane, and its sodium salt were also studied. Amidoximated grafted membranes and their copolymer–metal complexes of Cu(II) or Cr(III) were prepared. These membranes were characterized using different analysis techniques such as IR, UV and ESR spectrometry. The UV and ESR analyses revealed that the geometry structure for Cu(II) is square planar, while for Cr(III) it is octahedral. The amidoxime ligand was used for separating metal ions from aqueous solutions by a complexation process. The thermal stability of different membranes was investigated through TG analysis. It was found that the amidoxime‐grafted membranes possess good hydrophilic properties that may make them promising candidated for some practical applications such as the recovery of metals from their aqueous systems. © 2000 Society of Chemical Industry     

Synthesis and characterization of poly(hydroxamic acid)–poly(amidoxime) chelating ligands from polymer‐grafted acacia cellulose

Graft copolymerization of methyl acrylate (MA) and acrylonitrile (AN) onto acacia cellulose was carried out using free radical initiating process in which ceric ammonium nitrate (CAN) was used as an initiator. The optimum grafting yield was determined by the certain amount of acacia cellulose (AGU), mineral acid (H₂SO₄), CAN, MA, and AN at 0.062, 0.120, 0.016, 0.397, and 0.550 mol L^?1, respectively. The poly(methyl acrylate‐co‐acrylonitrile)‐grafted acacia cellulose was obtained at 55°C after 2‐h stirring, and purified acrylic polymer‐grafted cellulose was characterized by FTIR and TG analysis. Therein, the ester and nitrile functional groups of the grafted copolymers were reacted with hydroxylamine solution for conversion into the hydroxamic acid and amidoxime ligands. The chelating behavior of the prepared ligands toward some metal ions was investigated using batch technique. The metal ions sorption capacities of the ligands were pH dependent, and the sorption capacity toward the metal ions was in the following order: Zn²⁺ > Fe³⁺ > Cr³⁺ > Cu²⁺ > Ni²⁺. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Microwave preparation and adsorption properties of EDTA‐modified cross‐linked chitosan

A novel chitosan‐based adsorbent (CCTE) was synthesized by the reaction between epichlorohydrin O‐cross‐linked chitosan and EDTA dianhydride under microwave irradiation (MW). The chemical structure of this new polymer was characterized by infrared spectra analysis, thermogravimetric analysis, and X‐ray diffraction analysis. The results were in agreement with the expectations. The static adsorption properties of the polymer for Pb²⁺, Cu²⁺, Cd²⁺, Ni²⁺, and Co²⁺ were investigated. Experimental results demonstrated that the CCTE had higher adsorption capacity for the same metal ion than the parent chitosan and cross‐linked chitosan. In particular, the adsorption capacities for Pb²⁺ and Cd²⁺ were 1.28 mmol/g and 1.29 mmol/g, respectively, in contrast to only 0.372 mmol/g for Pb²⁺ and 0.503 mmol/g for Cd²⁺ on chitosan. Kinetic experiments indicated that the adsorption of CCTE for the above metal ions achieved the equilibrium within 4 h. The desorption efficiencies of the metal ions on CCTE were over 93%. Therefore, CCTE is an effective adsorbent for the removal and recovery of heavy metal ions from industrial waste solutions. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Molecular structure and ion exchange of amidoximated cellulosic materials

Modification of lignocellulosic materials, e.g., cotton stalks, bagasse, and rice straw, by incorporation of amidoxime group for ion exchange is investigated. The uptake of metal ions Cu, Cr, Ni, and Fe by these modified lignocellulosic materials is measured. Amidoximated bagasse has higher efficiency toward metal ions uptake than amidoximated cotton and rice straw. The effect of different variables, e.g., metal ion concentration, temperature of metal ion solution, and time of steeping, on the efficiency of the amidoximated (bagasse raw material, unbleached bagasse, and bleached bagasse) ion exchangers toward metal ions uptake is tested. The molecular structure of the prepared amidoxime from bagasse and its pulps is studied by using infrared spectroscopy. New bands appeared at 1661 and 916 cm^?1 in the spectra of amidoximated bagasse and its pulps ion exchangers due to the formation of C?N and N? OH groups. The thermal properties of these ion exchangers is also studied. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 303–311, 2006     

Preparation of amidoximated bacterial cellulose and its adsorption mechanism for Cu2+ and Pb2+

Amidoximated bacterial cellulose (Am‐BC) was prepared through successive polymer analogous reactions of bacterial cellulose with acrylonitrile in an alkaline medium followed by reaction with aqueous hydroxylamine. It was used as an adsorbent to remove Cu²⁺ and Pb²⁺ from aqueous solutions. The adsorption behaviors of Cu²⁺ and Pb²⁺ onto Am‐BC were observed to be pH‐dependent. The maximum adsorption capacity of 84 and 67 mg g^–1 was observed, respectively, for Cu²⁺ and Pb²⁺ at pH 5. Scanning electronic microscopy (SEM) indicated that the microporous network structure of Am‐BC was maintained even after the modifacation. The adsorption mechanisms for Cu²⁺ and Pb²⁺ onto Am‐BC were investigated by fourier transform infrared spectroscopy (FTIR), ζ potential measurement and X‐ray photoelectron spectroscopy (XPS). The results revealed that the mechanism for the adsorption of Cu²⁺ onto Am‐BC could be mainly described as between metal ions and nitrogen atom in the amidoxime groups or oxygen atom in the hydroxyl groups. However, in the adsorption process for Pb²⁺, precipitation played the important role along with electrostatic interactions, although chelation action also existed in the process accounted for the adsorption process. The regeneration of Am‐BC was studied by treatment with a strong complexing agent, ethylenediaminetetracetic acid (EDTA). © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Competitive removal of heavy metal ions by cellulose graft copolymers

The effect of composition of graft chains of four types cellulose graft copolymers on the competitive removal of Pb²⁺, Cu²⁺, and Cd²⁺ ions from aqueous solution was investigated. The copolymers used were (1) cellulose‐g‐polyacrylic acid (cellulose‐g‐pAA) with grafting percentages of 7, 18, and 30%; (2) cellulose‐g‐p(AA–NMBA) prepared by grafting of AA onto cellulose in the presence of crosslinking agent of N,N′‐methylene bisacrylamide (NMBA); (3) cellulose‐g‐p(AA–AASO₃H) prepared by grafting of a monomer mixture of acrylic acid (AA) and 2‐acrylamido‐2‐methyl propane sulphonic acid (AASO₃H) containing 10% (in mole) AASO₃H; and (4) cellulose‐g‐pAASO₃H obtained by grafting of AASO₃H onto cellulose. The concentrations of ions which were kept constant at 4 mmol/L in an aqueous solution of pH 4.5 were equal. Metal ion removal capacities and removal percentages of the copolymers was determined. Metal ion removal capacity of cellulose‐g‐pAA did not change with the increase in grafting percentages of the copolymer and determined to be 0.27 mmol metal ion/g_copolymer. Although the metal removal rate of cellulose‐g‐p(AA–NMBA) copolymer was lower than that of cellulose‐g‐pAA, removal capacities of both copolymers were the same which was equal to 0.24 mmol metal ion/g_copolymer. Cellulose did not remove any ion under the same conditions. In addition, cellulose‐g‐pAASO₃H removed practically no ion from the aqueous solution (0.02 mmol metal ion/g_copolymer). The presence of AASO₃H in the graft chains of cellulose‐g‐p(AA–AASO₃H) created a synergistic effect with respect to metal removal and led to a slight increase in metal ion adsorption capability in comparison to that of cellulose‐g‐pAA. All types of cellulose copolymers were found to be selective for the removal of Pb²⁺ over Cu²⁺ and Cd²⁺. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2034–2039, 2003     

Electron Beam Grafted Polymer Adsorbent for Removal of Heavy Metal Ion from Aqueous Solution

Abstract

An electron beam grafted adsorbent was synthesized by post irradiation grafting of acrylonitrile (AN) on to a non‐woven thermally bonded polypropylene (PP) sheet using 2 MeV electron beam accelerator. The grafted poly(acrylonitrile) chains were chemically modified to convert a nitrile group to an amidoxime (AMO) group, a chelating group responsible for metal ion uptake from an aqueous solution. The effect of various experimental variables viz. dose, dose rate, temperature, and solvent composition on the grafting extent was investigated. PP grafted with the amidoxime group (AMO‐g‐PP) was tested for its suitability as an adsorbent for removal of heavy metal ions such as Co²⁺, Ni²⁺, Mn²⁺, and Cd²⁺ from aqueous solution. Langmuir and Freundlich adsorption models were used to investigate the type of adsorption of these ions. The adsorption capacities of the adsorbent for the metal ions were found to follow the order Cd²⁺>Co²⁺>Ni²⁺>Mn²⁺. The kinetics of adsorption of these ions indicated that the rate of adsorption of Cd²⁺ was faster than that of other ions studied.     

Adsorption removal of Cu2+ and Ni2+ from waste water using nano‐cellulose hybrids containing reactive polyhedral oligomeric silsesquioxanes

Cellulose is an important biomass in natural material fields. Reactive polyhedral oligomeric silsesquioxane (R‐POSS) bearing multi‐N‐methylol groups is novel high reactive POSS monomer. The nano‐cellulose hybrids containing R‐POSS were synthesized by crosslinking reaction. It was interesting to investigate properties and applications of hybrids containing R‐POSS. In this work, nano‐cellulose hybrids as novel biosorbent were used for adsorpting copper and nickel ions in aqueous solution. Adsorption kinetics and equilibrium isotherm of Cu²⁺ and Ni²⁺ on the nano‐cellulose hybrids were investigated. The results showed that R‐POSS had been grafted to cellulose macromolecule. The nano‐cellulose hybrids could form new adsorptive position for heavy metal ions. The adsorption capacities of hybrid materials were obviously higher than that of control cellulose. The adsorption of heavy metal ions on nano‐cellulose hybrids followed the second‐order model. The equilibrium isotherms for adsorpting copper and nickel ions on the hybrids followed Langmuir isotherm model. Nano‐cellulose materials containing POSS as biosorbents or ultrafiltration membranes would be used in separation of toxic heavy metal ions. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

Development of amidoxime functionalized silica by radiation‐induced grafting

A novel amidoxime‐based silica adsorbent was prepared by using radiation‐induced grafting technique. Grafting of acrylonitrile (AN) on silanized silica that was silanized by vinyltriethoxysilane (VTES) was carried out in solvent‐free system. The grafting of AN was increased with increasing the absorbed dose and monomer concentration in the mixture. Grafting of 748% of AN was achieved at 20 kGy dose. The nitrile groups of acrylonitrile grafted silica (AN‐g‐S) were chemically converted into amidoxime groups. The structure of AN‐g‐S and its corresponding products was investigated by FTIR, SEM, TGA, BET, and XRD analysis. FTIR and EDX analysis confirmed the grafting of AN onto silica surface. The changed morphology of SEM images shows the presence polyacrylonitrile layers on silica particles. The adsorption application of amidoxime‐grafted silica (AO‐g‐S) was studied against Cu²⁺. Its adsorption capacity is strongly depended on the pH of the solution and 172 (mg/g) of Cu²⁺ uptake was obtained at pH 5.0. The developed adsorbent has potential application to remove heavy metal ions from aqueous solutions. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45437.     

Preparation and coordination behavior of cellulose beads derivative modified by 1,5‐diaminoethyl‐3‐hydroxy‐1,5‐diazacycloheptane

Cellulose derivative (MPCN) modified by 1,5‐diaminoethyl‐3‐hydroxy‐1,5‐diazacycloheptane (DADN) was prepared and characterized by scanning electron microscopy and elemental, and infrared analysis. MPCN and its Cu²⁺, Pb²⁺ complexes were characterized by thermogravimetric and differential thermal analysis. The coordination adsorption behavior of MPCN with divalent copper and lead ions was determined. The effects of temperature, initial pH value, and the concentration of MPCN ligand to the equilibrium adsorption were discussed. The optimum pH range of the coordination adsorption of MPCN with Cu²⁺ and Pb²⁺ is 5–6. The rate constants of the coordination reaction were found. At 323 K, the rate constant is 1.0 × 10⁻³ and 7.0 × 10⁻⁴ s⁻¹ for Cu²⁺ and Pb²⁺, respectively. The thermodynamic parameters of the coordination reaction were obtained based on the experiment data of the adsorption isotherms. The coordination reaction was performed spontaneously from the data of ΔG, as follows: −21.65 and −19.41 kJ/mol and ΔS, 87.06 and 67.92 J/mol K for Cu²⁺ and Pb²⁺, respectively. The coordination ratio of DADN coordination group immobilized on cellulose beads with either metal ion is about 1 : 2 from the plot of the relation of lgD versus lgL and the capacity of saturation adsorption. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 1278–1285, 1999     

Recent developments in the radiation grafting of N‐vinyl‐2‐pyrrolidone onto low‐density polyethylene with cinnamonitrile derivatives

The radiation‐induced graft polymerization of N‐vinyl‐2‐pyrrolidone onto low‐density polyethylene films was conducted with γ radiation by a simultaneous technique. The grafted copolymer was modified with cinnamonitrile or benzylidene malononitrile. The modified and grafted films were amidoximated with hydroxylamine hydrochloride in a basic medium. However, during amidoximation, the benzylidene malononitrile was cyclized to yield isoxazole ring through an addition to the nitrile group in its structure, whereas the nitrile groups of cinnamonitrile were converted into amidoxime groups. The swelling behavior of the grafted copolymers and copolymers grafted and modified either with cinnamonitrile or benzylidene malononitrile was studied. Amidoximated and grafted films and copolymer–metal complexes of Cu(II) were prepared and characterized. The effect of the isoxazole ring on polymeric materials was also investigated. These films were characterized with different analysis techniques, such as infrared, ultraviolet (UV), elemental analysis, energy‐dispersive spectroscopy, and electron spin resonance (ESR). The UV and ESR analyses revealed that the geometric structure of Cu(II) was square‐planar. Scanning electron microscopy was used to examine the grafted and modified films to determine the changes in the surface morphology. Morphological changes clearly appeared for both complexed and isoxazole films because of the increase in their crystallinity. The thermal stability of different films was investigated with thermogravimetric analysis. The improvement of the copolymer by modification with cinnamonitrile derivatives showed great promise for some practical applications, such as metal recovery by complexation or the use of isoxazole in medicine. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 95: 1189–1197, 2005     

Adsorption of copper(II) and chromium(III) ions onto amidoximated cellulose

Chemical modification of cellulose powder is performed by successive reactions with acrylonitrile in an alkaline medium followed by aqueous hydroxylamine to prepare amidoximated cellulose. Due to complexation, the amidoxime groups immobilize heavy cations from buffered solutions at various pH values. The capacity of adsorption for Cu(II) and Cr(III) ions is related to the amount of amidoxime groups in the support and to the metal concentration of the polluted solution. The formation of a 1/1 complex is proved by the adsorption limit values. Desorption of the cations is possible by treatment with a stronger complexing agent such as ethylenediaminetetracetic acid. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 75: 1624–1631, 2000     

Uranyl ion adsorptivity of N-vinyl 2-pyrrolidone/acrylonitrile copolymeric hydrogels containing amidoxime groups

Summary N-vinyl 2-pyrrolidone (VP) / Acrylonitrile (AN) copolymeric hydrogels were synthesized by using γ-radiation and amidoximated for the purpose of uranyl ion adsorption. Optimum amidoximation time was determined by following the uranyl ion, UO₂ ²⁺, adsorption capacity. The adsorption of amidoximated copolymers was studied from different uranyl ion solutions (1000–1850 ppm). The results of all adsorption studies showed that the interaction between UO₂ ²⁺ and amidoxime groups comply with Langmuir type isotherm. The adsorption capacity was found as 0.54 g UO₂ ²⁺ /g dry amidoximated copolymeric hydrogels. From the stoichiometric calculations, it was found that the bonding between UO₂ ²⁺ and amidoxime groups is 1 to 4. Received: 7 September 1999/Revised version: 21 February 2000/Accepted: 18 March 2000     

Thiourea modified hyper‐crosslinked polystyrene resin for heavy metal ions removal from aqueous solutions

A hyper‐crosslinked resin chemically modified with thiourea (TM‐HPS) was synthesized, characterized, and evaluated for the removal of heavy metal ions (Pb²⁺, Cd²⁺, and Cu²⁺) from aqueous solutions. The structural characterization results showed that a few thiourea groups were grafted on the surface of the resin with a big BET surface area and a large number of narrow micropores. Various experimental conditions such as pH, contact time, temperature, and initial metal concentration of the three heavy metal ions onto TM‐HPS were investigated systematically. The results indicated that the prepared resin was effective for the removal of the heavy metal ions from aqueous solutions. The isotherm data could be better fitted by Langmuir model, yielding maximum adsorption capacities of 689.65, 432.90, and 290.69 mg/g for Pd²⁺, Cd²⁺, and Cu²⁺, respectively. And the adsorption kinetics of the three metal ions followed the pseudo‐second‐order equation. FTIR and XPS analysis of TM‐HPS before and after adsorption further revealed that the adsorption mechanism could be a synergistic effect between functional groups and metal ions and electrostatic attraction, which may provide a new insight into the design of highly effective adsorbents and their potential technological applications for the removal of heavy metal ions from aqueous solutions. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45568.     

Removal of phosphate ions with a chemically modified chitosan/metal‐ion complex

The adsorption of metal ions (Mo⁶⁺, Cu²⁺, Fe²⁺, and Fe³⁺) was examined on chemically modified chitosans with a higher fatty acid glycidyl (CGCs), and the adsorption of Cu²⁺ was examined on ethylenediamine tetraacetic acid dianhydride modified CGCs (EDTA‐CGCs) synthesized by the reaction of the CGCs with ethylenediamine tetraacetic acid dianhydride. The adsorption of phosphate ions onto the resulting substrate/metal‐ion complex was measured. Mo⁶⁺ depicted remarkable adsorption toward the CGCs, although all the Mo⁶⁺ was desorbed under the adsorption conditions of the phosphate ions. The other metal ions were adsorbed to some extent on CGCs by chelating to the amino group in the substrate, except for CGC‐1, which had the highest degree of substitution (83.9%). Considerable amounts of Fe²⁺ were adsorbed onto CGCs; however, only a limited number of phosphate ions was adsorbed onto the substrate/metal‐ion complex. As a result, the following adsorbent/metal‐ion complexes gave higher adsorption ability toward phosphate ions: CGC‐4/Cu²⁺, CGC‐4/Fe³⁺, and EDTA‐CGC‐3/Fe³⁺. Where, CGC‐3 is a chemically modified chitosan with the degree of substitution of 26.5 percentage, and CGC‐4 is one with the degree of substitution of 16.0 percentage. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Study on quaternary ammonium modified tentacle‐type cellulose beads and its adsorption for

A novel anion exchange resin based on cellulose has been prepared to adsorb for the urgent demand of silver and the high toxicity of metal‐cyanide complexes. Quaternary ammonium groups were grafted onto cellulose beads as main active sites in tentacle‐type through a series of chemical reactions. The substitution degree of each reaction was determined to be about 0.854, 2.125, and 2.899 mmol g^?1, respectively. The resin exhibited excellent spherical shape with microporous structure by the observation of optical microscopy and scanning electron microscope. Moreover, the adsorption experiments demonstrated the adsorption was fast in alkaline condition. Fitting the data into isotherm and kinetic models gave the conclusion that the adsorption behavior matched better with Langmuir model and pseudo‐second‐order kinetic in initial time followed pseudo‐first‐order kinetic model in later phase. The equilibrium adsorption capacity was determined to be 3.016 mmol g^?1. With the advantages of high capacity, short equilibrium time, and alkaline resistance, the resin would be considered to a top‐priority adsorbent for the separation of . © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40987.