Poly(2‐hydroxyethylmethacrylate)/chitosan dye and different metal‐ion‐immobilized interpenetrating network membranes: Preparation and application in metal affinity chromatography

Composite membranes were synthesized with 2‐hydroxyethylmethacrylate and chitosan (pHEMA/chitosan) via an ultraviolet‐initiated photopolymerization technique in the presence of an initiator (α,α′‐azobisisobutyronitrile). The interpenetrating network (IPN) membranes were improved by the immobilization of dye molecules via hydroxyl and amino groups on the membrane surfaces from the IPNs. A triazidine dye (Procion Green H‐4G) was covalently immobilized as a ligand onto the IPN membranes. The protein showed various affinities to different chelated metal ions on the membrane surfaces that best matched its own distribution of functional sites, resulting in a distribution of binding energies. In support of this interpretation, two different metal ions, Zn(II) and Fe(III), were chelated with the immobilized dye molecules. The adsorption and binding characteristics of the different metal‐ion‐chelated dye‐immobilized IPN membranes for the lysozyme were investigated with aqueous solutions in magnetically stirred cells. The experimental data were analyzed with two adsorption kinetic models, pseudo‐first‐order and pseudo‐second‐order, to determine the best fit equation for the adsorption of lysozyme onto IPN membranes. The second‐order equation for the lysozyme–dye–metal‐chelated IPN membrane systems was the most appropriate equation for predicting the adsorption capacity for all the tested adsorbents. The reversible lysozyme adsorption on the dye‐immobilized and metal‐ion‐chelated membranes obeyed the Temkin isotherm. The lysozyme adsorption capacity of the pHEMA/chitosan dye, pHEMA/chitosan dye–Zn(II), and pHEMA/chitosan dye–Fe(III) membranes were 2.54, 2.85, and 3.64 mg cm^?2, respectively. The nonspecific adsorption of the lysozyme on the plain pHEMA/chitosan membrane was about 0.18 mg cm^?2. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1843–1853, 2003     

Dye removal from colored textile wastewater using chitosan in binary systems

In this paper, the removal of two anionic dyes from textile effluent in single and binary systems was investigated. Direct Red 23 and Acid Green 25 were used as anionic dyes. The surface characteristics of chitosan were investigated using Fourier transform infrared. The effects of operational parameters such as chitosan dosage, initial dye concentration, salt and pH on dye removal were studied. The isotherms of dye adsorption were investigated. It was found that the isotherm data of Direct Red 23 and Acid Green 25 in single and binary systems followed Tempkin isotherm. In addition adsorption kinetics of dyes was studied in single and binary systems and rate sorption was found to conform to pseudo-second order kinetics with a good correlation. Results indicated that chitosan could be used as a biosorbent to remove the anionic dyes from contaminated watercourses in both single and binary systems of pollutants.     

生物质对低浓度染料废物的协同多层吸收(英文)

Due to the high cost of adsorbents and their thermal regeneration in recent years,much research has focused on the search for cheaper adsorbents for treating wastewater from textile industry.The single component adsorption of an acidic dye,Acid Yellow 117,and a basic dye,Methylene Blue,onto several adsorbents—bamboo,waste wood,bamboo char,waste wood char,bamboo activated carbon,wood activated carbon and active carbon F400 were conducted.Based on a Langmuir analysis,the monolayer adsorption capacities were determined.Three of the adsorbents were selected for binary layer adsorption to check the multilayer concept and the potential application for better adsorbent usage.The two cheapest adsorbents,bamboo and wood are compared with the commercial activated carbon F400,and all three systems were successful.     

Beta-cyclodextrin adsorbents to remove water pollutants—a commentary

Beta-cyclodextrin-based adsorbent is a promising adsorbent because it has unique characteristics and able to form host-guest complexes with various organic compounds. Adsorption using beta-cyclodextrin-based adsorbent has continuously improved by various preparation strategies and crosslinking agents. This commentary aims to highlight the preparation strategies, properties, and adsorption mechanisms of beta-cyclodextrin-based adsorbents. The adsorbents can be generally classified according to the preparation methods and display high adsorption capacity especially for dyes. Particularly, composite/nanocomposite beta-cyclodextrin-based adsorbents exhibit outstanding adsorption capacity even though the surface area is lower than that of porous and magnetic beta-cyclodextrin-based adsorbents. The beta-cyclodextrin/chitosan functionalized graphene oxide hydrogel with specific surface of 17.6 m²·g^–1 yields an extraordinarily maximum adsorption capacity of 1499 mg·g^–1 methylene blue, while beta-cyclodextrin/chitosan modified with iron(II, III) oxide nanoparticles displays a much greater maximum adsorption capacity at 2780 mg·g^–1. The hydrophobic interaction, functional groups, hydrogen bonding, and electrostatic interaction govern the adsorption to a greater capacity. Although this commentary is not exhaustive, the preparation strategies and illustrated mechanisms provide useful insights into the adsorbent–adsorbate interactions, cost-effective analysis, challenges, and future directions of beta-cyclodextrin-based adsorbents in wastewater treatment.     

A novel nonchemical approach to the expansion of halloysite nanotubes and their uses in chitosan composite hydrogels for broad‐spectrum dye adsorption capacity

A novel method based on cryoscopic expansion of halloysite nanotubes via frozen water molecules entrapped in their lumens and subsequent lyophilization was described. Detailed analyses confirmed that the inner and outer diameters as well as the surface area of the nanotubes could be efficiently increased without disturbing the inherent tubular structure. The benefits of cryo‐expanded nanotubes for the enhancement of chitosan hydrogel performances were discussed. The composite hydrogels, depending on their compositions and morphologies, exhibited significantly enhanced swelling and mechanical properties compared with neat chitosan hydrogel. This effect was even more pronounced in the hydrogels containing cryo‐expanded halloysite nanotubes. Although neat chitosan is a selectively good adsorbent for anionic dyes, in the presence of a small amount of cryo‐expanded halloysite, the resultant composite hydrogel can establish a relatively high adsorption capacity for anionic and cationic dyes as a broad‐spectrum dye adsorbent. POLYM. COMPOS., 37:2770–2781, 2016. © 2015 Society of Plastics Engineers     

Adsorption Behavior of Methylene Blue from Aqueous Solution by the Hydrogel Composites Based on Attapulgite

A series of carboxymethyl cellulose-g-poly (acrylic acid)/attapulgite hydrogel composites were synthesized for the removal of cationic dye methylene blue. Various factors affecting the uptake behavior were investigated. Adsorption rate of the hydrogel was quite fast, and adsorption equilibrium could be reached within 30 min. Adsorption kinetics well followed the pseudo-second-order equation for all systems. The Langmuir isotherm was found to best represent the data for the dye uptake. Even when 20 wt% attapulgite was introduced into the hydrogel, the corresponding maximum adsorption capacity reached 1979.48 mg/g at 30°C. The as-prepared adsorbents exhibited excellent affinity for the dye, and can be applied to treat wastewater containing basic dyes.     

Cu2+ removal from aqueous solution by modified chitosan hydrogels

BACKGROUND: The adsorption of Cu²⁺ from aqueous solution using crosslinked chitosan hydrogels impregnated with Congo Red (CR) by ion‐imprint technology was systematically investigated with particular reference to the effects of contact time, pH, and initial concentration on adsorption. RESULTS: The adsorption capacity of the crosslinked chitosan without impregnation was only 68.68 mg g^?1 for Cu²⁺. However, the adsorption capacity increased from 77.42 (without imprint ion) to 84.54 mg g^?1 (imprint ion content 0.5 mmol) after the chitosan was impregnated with a ratio of 1/12 of CR to chitosan. The as‐prepared adsorbents were found to be pH‐dependent and the process of adsorption agreed well with the Freundlich isotherm. The loaded adsorbents could be regenerated and reused without the appreciable loss of capacity. CONCLUSION: Chitosan hydrogels impregnated with CR showed higher Cu²⁺ adsorption capacities compared with those prepared conventionally without imprint ion, and thus developed a good approach to increase Cu²⁺ adsorption efficiency in the treatment of waste‐water. Copyright © 2012 Society of Chemical Industry     

Adsorption equilibria between dye and surfactant in single and binary systems onto geological materials

Adsorption characteristics of cationic dyes and surfactants onto clay and sandstone from a single component system were studied using toluidine blue (TB) and cetyl trimethylammonium bromide (CTAB). Equilibrium data of TB and CTAB in the single solute systems fit well to the Langmuir and the Freundlich adsorption isotherms. Competitive adsorption was observed between dye and surfactant cations. The effect of sodium chloride on dye and surfactant adsorption was studied in TB–NaCl and CTAB–NaCl binary systems. Equilibrium adsorption for binary systems was analyzed by using the extended Langmuir and the extended Freundlich models. Adsorption results for the TB–CTAB system onto both adsorbents were also well described by the Sheindorf–Rebuhn–Sheintuch (SRS) model for multi-component systems. Free energy changes for adsorption systems were calculated using thermodynamic equilibrium constants evaluated from selectivity coefficients of the binary systems. The site distribution functions estimated using Freundlich model parameters gave valuable information about the ratio of the adsorption sites on adsorbent surface having different affinity for competing cations.     

Integrated three‐dimensional fiber/hydrogel biphasic scaffolds for periodontal bone tissue engineering

Combining a tissue engineering scaffold made of a load‐bearing polymer with a hydrogel represents a powerful approach to enhancing the functionalities of the resulting biphasic construct, such as its mechanical properties or ability to support cellular colonization. This research activity was aimed at the development of biphasic scaffolds through the combination of an additively manufactured poly(?‐caprolactone) (PCL) fiber construct and a chitosan/poly(γ‐glutamic acid) polyelectrolyte complex hydrogel. By investigating a set of layered structures made of PCL or PCL/hydroxyapatite composite, biphasic scaffold prototypes with good integration of the two phases at the macroscale and microscale were developed. The biphasic constructs were able to absorb cell culture medium up to 10‐fold of their weight, and the combination of the two phases had a significant influence on compressive mechanical properties compared with hydrogel or PCL scaffold alone. In addition, due to the presence of chitosan in the hydrogel phase, biphasic scaffolds exerted a broad‐spectrum antibacterial activity. The developed biphasic systems appear well suited for application in periodontal bone regenerative approaches in which a biodegradable porous structure providing mechanical stability and a hydrogel phase functioning as absorbing depot of endogenous proteins are simultaneously required. © 2016 Society of Chemical Industry     

Surfactant‐modified feldspar: Isotherm,kinetic, and thermodynamic of binary system dye removal

In this article, surface modification of feldspar using hexadecyltrimethyl ammonium bromide (HDTMA) and its dye removal ability in single and binary systems was studied. Acid Black 1 (AB1) and Acid Red 14 (AR14) were used as model dyes. The monocomponent Langmuir isotherm model was applied to experimental data and the isotherm constants were calculated for both dyes. The monolayer coverage capacities of surfactant‐modified feldspar (HDTMA‐feldspar) for AB1 and AR14 dyes in single solution system were found as 6.369 mg/g and 3.984 mg/g, respectively. It was observed that the equilibrium uptake amounts of AB1 and AR14 dye in binary mixture onto sorbent decreased with increasing concentrations of the other dye resulting in their antagonistic effect. Equilibrium adsorption for binary systems was analyzed by using the Extended Langmuir and Jain and Snoeyink Modified Extended Langmuir models. The rate of kinetic processes of single and binary dye systems onto adsorbent was described by using two kinetics adsorption models. The pseudo‐second‐order model was the best choice among the kinetic models to describe the adsorption behavior of single and binary dyes onto HDTMA‐feldspar. Thermodynamic parameters showed that dye adsorption on HDTMA‐feldspar were exothermic and unspontaneous in nature. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Competitive adsorption of acid dyes from aqueous solution on diethylenetriamine‐modified chitosan beads

The interaction between two dyes (AO7 and AG25) during adsorption was studied in detail with diethylenetriamine‐modified chitosan beads (CTSN‐beads) as the adsorbent. Results indicate that the adsorption capacities and rates were directly related to the molecular size of the dye. The adsorption capacity and rate of AO7 could be greatly weakened by interaction with AG 25 during adsorption, which has a larger molecular size. The adsorption followed the pseudo‐second‐order kinetic equation and Freundlich model gave a satisfying correlation with the equilibrium data both in the single and binary component system. Adsorption could be divided into three stages, each controlled by different mechanisms. Temperature experiments showed high temperature was beneficial to the mass transfer of dyes. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41168.     

Adsorption behavior of reactive dyes from aqueous solutions on chitosan

The capability of the use of chitosan for removing vinyl sulfone and chlorotriazine reactive dyes from aqueous solutions was examined, including equilibrium and dynamic studies. Experiments were performed as a function of dye concentration, and the amount and particle size of chitosan. It was shown that the adsorption capacities of chitosan were comparatively high for the three investigated dyes. The equilibrium data could be best fitted by the Redlich–Peterson equation over the entire concentration range (50–500 g m⁻³). A comparison of the adsorption capacity among such adsorbents as chitin and powdered activated carbon was made. Two rate parameters were finally obtained to describe the adsorption process on a quantitative basis. These parameters could be well correlated to the amount and particle size of dry chitosan. ©1997 SCI     

Utilization of polyampholyte hydrogels for simultaneous removal of textile dyes from aqueous solutions

The study aimed to create hydrogel structures with greater functionality, otherwise known as polyampholytes (PAHs), and to use these in simultaneous removal studies for remazol-type dyes found in environmental waste waters. Adsorption studies were accomplished at 20°C and 35°C, indicated that adsorption process was exothermic in nature. The Q_m values for the PAH-dye systems were in the interval 111–122 mg dye/g PAH with Ads% from 94% to 98%. The ability of PAH hydrogels to adsorb two different species of dye molecules at the same time is an advantage of PAH adsorbents compared to other hydrogel adsorbents prepared in this area.     

Preparation of an ecofriendly chitosan–ZnO composite for chromium complex dye adsorption

Three chitosan‐ZnO composites were prepared by the chitin deacetylation process using zinc chloride as source material and sodium hydroxide as precipitant. The physical characteristics of chitosan‐ZnO composites were studied using Fourier Transform infrared spectroscopy and scanning electron microscopy. The adsorption of a chromium complex dye onto commercial chitosan, prepared chitosan and chitosan‐ZnO composites was investigated in aqueous dye solution. Dye calibration was carried out by UV‐vis spectroscopy. The calculated dye adsorption values for commercial chitosan, prepared chitosan, and chitosan‐ZnO composite samples are 0.0086, 0.0137, and 0.0214 mg/g respectively, indicating that the chitosan‐ZnO composites have better dye adsorption capacity than commercial chitosan and prepared chitosan. The experimental isotherm data for the composites fitted the Langmuir isotherm model well. Thus, the chitosan‐ZnO composites can be used as an effective biosorbent for the removal of anionic dyes.     

Removal of methylene blue from aqueous solution by sorption on lignocellulose-g-poly(acrylic acid)/montmorillonite three-dimensional cross-linked polymeric network hydrogels

Batch lignocellulose-g-poly(acrylic acid)/montmorillonite (LNC-g-PAA/MMT) hydrogel nanocomposites were applied as adsorbents. The nanocomposites were characterized by FTIR, XRD, SEM, and TEM. The results showed that montmorillonite (MMT) could react with the monomers and change the structure of polymeric network of the traditional superabsorbent materials, an exfoliated structure was formed in the nanocomposites. The effect of process parameters such as MMT content (wt%), contact time (t), initial concentration of dye solution (C ₀), adsorption temperature (T), and pH value (pH) of the dye solution for the removal of methylene blue (MB) from aqueous solution were also studied. The results showed that the adsorption capacity for MB increased with increasing contact time, initial dye concentration, and pH value, but decreased with increasing MMT content and temperature. The adsorption kinetics were better described by the pseudo-second-order equation, and their adsorption isotherms were better fitted for the langmuir equation. By introducing 20 wt% MMT into LNC-g-PAA polymeric network, the obtaining hydrogel composite showed the high adsorption capacity 1994.38 mg/g and economic advantage for MB. The desorption studies revealed that the composite provided the potential for regeneration and reuse after MB dye adsorption, which implied that the composite could be regarded as a potential adsorbent for cationic dye MB removal in a wastewater treatment process.     

Adsorption Behavior of Anionic Reactive Dyes on H‐type Activated Carbon: Competitive Adsorption and Desorption Studies

Abstract

A microporous H‐type activated carbon was shown to be effective for removing anionic reactive dyes from single and binary component solutions. The extent of the dye adsorption from a single‐solute solution was high (0.25–0.42 mmol/g). From the binary dye solutions, the experimental data indicated a high degree of competition for active sites and the obtained adsorption capacities were reduced to 0.10–0.26 mmol/g. Adsorption data from single dye solutions were correlated using the Langmuir, Ferundlich, and Redlich‐Peterson models. Hydrophobic, hydrophobic mechanisms were significant in the adsorption process. Furthermore, the system showed a low extent of desorption.     

Radiation-initiated chitosan-based double network hydrogel: Synthesis,characterization, and adsorption of methylene blue

A novel chitosan (CTS)-based double network Poly(2-acrylaMido-2-Methyl-1-propanesulfonic acid)/Polyacrylamide/CTS hydrogel was synthesized by irradiation initiated. Laponite RD (RD) was used as both dopant and the cross-linking agent. Then the fabricated hydrogel was applied as an efficient adsorbent to remove the methylene blue (MB) in an aqueous solution. This hydrogel has both high strength and good adsorption properties for MB. The results from Brunauer–Emmett–Teller method confirmed that the hydrogel has a large specific surface area (96 m²/g) and developed pore structure, which is available for the contact between the adsorbent and dye molecules. In the adsorption process, the RD provides plenty of negative charges as adsorption sites for MB molecules. The influence of pH, temperature, and adsorbent dose on the adsorption performance was investigated in detail. The experimental data fit well with the pseudo-second-order kinetic model and Langmuir isotherm. Besides, the mechanical strength of the hydrogel was also investigated in this work.     

Poly(acrylic acid)/poly(acrylamide) hydrogel adsorbent for removing methylene blue

Cationic dye can cause severe damage to the environment due to their refractory degradation, complex composition and strong stability. Hydrogels as adsorbents have been widely used to treatment the wastewater with dyestuff for their low prices, simple operations, and high efficiency. This work uses poly(acrylic acid) (PAA)/poly(acrylamide)(PAM)/calcium hydroxide nanoparticles (CHN) polymeric hydrogel absorbent to eliminate methylene blue (MB) dye. First, PAM/PAA/CHN hydrogel is produced through copolymerization of acrylic acid monomer and acrylamide monomer using inorganic CHN as cross-linker. And then, the adsorption performance of such PAM/PAA/CHN hydrogel adsorbent for adsorbing MB dye is explored at different conditions including pH, contacting time, adsorbent dosage, initial concentration of MB, and temperature. A maximum adsorption capability for adsorbing MB reaches 1,056 mg/g. Furthermore, the pseudo-first-order mode and Langmuir isotherm model can well describe adsorption behavior of MB dye onto such PAA/PAM/CHN hydrogel adsorbent. Thereby, as-prepared PAA/PAM/CHN hydrogel could be a potential adsorbent for eliminating organic dyes from wastewater.     

Synthesis of Cibacron Blue F3GA‐coupled magnetic PMMA nanospheres and their use for protein affinity separation

BACKGROUND: New magnetic carrier separation technologies, capable of treating dilute solutions in large‐scale processes, even in the presence of biological debris, are necessary for the future development of biotechnology. Non‐porous magnetic carriers are more resistant to fouling, show better mass transfer and have lower non‐specific adsorption than porous carriers. Nanosized magnetic carriers have a surface area comparable to that of typical macroporous resins, and therefore their application has advantages. RESULTS: Magnetic poly(methyl methacrylate) (PMMA) nanospheres with an average diameter of 76 nm and narrow size distribution were prepared by a facile mini‐emulsion polymerization. After surface modification with poly(ethylene glycol), Cibacron Blue F3GA (CB) was coupled to the magnetic PMMA nanospheres to form dye ligand‐attached magnetic adsorbents for bovine serum albumin (BSA) adsorption. The CB‐coupled magnetic PMMA nanospheres showed very high adsorption capacity (121.98 mg g^?1) and little non‐specific adsorption for BSA. The adsorbed protein could be easily desorbed using high ionic strength solution. CONCLUSION: The CB‐coupled magnetic PMMA nanospheres showed a high BSA adsorption capacity, low non‐specific adsorption and fast adsorption kinetics in comparison with other dye‐affinity adsorbents. These characteristics indicate that these magnetic PMMA nanospheres have great potential for protein affinity separation and purification. Copyright © 2009 Society of Chemical Industry     

Synthesis of hydrogels from fractionated proteins of Moringa oleifera Lam. seeds for the treatment of water contaminated with black reactive dye 5

As has been portrayed in the literature, the main proteins extracted from the seeds of Moringa oleifera Lam. have coagulant and clarifying potential in water treatment. However, when using them as coagulant agents, sludge formation occurs, which is an environmental problem. Thus, it was proposed to synthesize hydrogels from the main Moringa seeds proteins and use them as adsorbents. This work aimed to synthesize albumin hydrogels and globulin hydrogels and evaluate their efficiency as adsorbents to remove the reactive black 5 dye. Through FTIR spectrum it was possible to confirm that the synthesis of hydrogels occurred successfully. The kinetic data fit the pseudo-second order model for both hydrogels. The equilibrium isotherms showed that adsorption occurs in multilayers, due to Freundlich fitting. The maximum adsorption capacity occurred at 298 K and was 1.19 mg g⁻¹ for the albumin hydrogel and 10.06 mg g⁻¹ for the globulin hydrogel. Through the results it is possible to state that globulin hydrogel was more favourable for adsorption since it has a more porous morphology and requires less mass compared to albumin hydrogel.