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At least 181 records · Page 10

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DOE OSTI2017

Effect of Varying Filler Concentration on Zinc Oxide Nanoparticle Embedded Chitosan Films as Potential Food Packaging Material

Prevailing scenario of non-biodegradable food packaging materials worldwide was the motivation for this research. More than half of the packaging materials used today are non-biodegradable and lack one or the other feature that keeps it from being an ideal food packaging material. Based on the current need of food grade packaging materials, the present study illustrates the amelioration of the properties of biodegradable chitosan films with the incorporation of zinc oxide (ZnO) nanoparticles in varying concentration. The ZnO nanoparticles (ZnONPs) used as fillers in the chitosan films were synthesized by supersaturation method. They were characterized using UV–visible spectrophotometry, X-ray diffraction and field emission scanning electron microscopy (FE-SEM). The particles were observed to be around 100–200 nm in size. The chitosan films with varying concentration of ZnONPs were synthesized and characterized using Fourier transform infrared spectroscopy and FE-SEM. The films were studied for their thermal stability, water vapor transmission rate (WVTR) and mechanical properties. The thermal stability, as determined by Thermo Gravimetric Analysis and Differential Scanning Calorimetry increased slightly with increasing percentage of embedded ZnONPs while a substantial decrease in WVTR was observed. Mechanical properties also showed improvements with 77% increment in tensile modulus and 67% increment in tensile strength. The antimicrobial activity of the films was also studied on gram positive bacterium Bacillus subtilis (B. subtilis) and gram negative bacterium Escherichia coli (E. coli) by serial dilution method. A twofold and 1.5-fold increment in the antimicrobial activity was observed for B. subtilis and E. coli, respectively, with increased ZnONPs concentration in the films from 0(w/w) to 2%(w/w). Films thus prepared can prove to be of immense potential in the near future for antimicrobial food packaging applications.

36 MATERIALS SCIENCE↗

DOE OSTI2017

The Gene of Aspergillus oryzae Involved in Degradation of Formaldehyde and Formaldehyde Degradation in Vapour Phase by Porous Enzyme/Chitosan Nanofibre Composites

Volatile organic compounds (VOCs) are toxic chemicals, detrimental to humans and the environment. Currently, there is no fully satisfactory method for VOC removal from indoor air. Formaldehyde, a well-known and ubiquitously present VOC, should be removed because of its various adverse effects on human health. In this study, we developed a method for removal of formaldehyde using porous enzyme/chitosan nanofibre composites. To identify the gene for a formaldehyde-degrading enzyme, we examined the involvement of the alcohol dehydrogenase gene (alcA) of Aspergillus oryzae in formaldehyde degradation. Using an alcA-disrupted strain, we found that formaldehyde degradation was lower in this mutant strain than in the control strain, suggesting that this enzyme played an essential role in formaldehyde degradation. Next, we assessed the ability of the crude enzyme extracted from A. oryzae to degrade formaldehyde in vitro. The enzyme showed a formaldehyde degradation rate of 50 ppm in 30 h. We then produced porous enzyme/chitosan nanofibre composites by mixing the crude enzyme and a 10% (w/v) chitosan nanofibre suspension, followed by freeze-drying. Characterization of the enzyme/chitosan nanofibre composites was carried out by X-ray photoelectron spectroscopy. Formaldehyde degradation tests were carried out using porous chitosan nanofibre and porous enzyme/chitosan nanofibre composites. Based on this analysis, we found that the porous enzyme/chitosan nanofibre composites showed a greater formaldehyde degradation ability than that of the porous chitosan nanofibres. When using the porous enzyme/chitosan nanofibre composites, formaldehyde was efficiently removed via enzymatic degradation and chemical adsorption by chitosan. These findings suggested that porous enzyme/chitosan nanofibre composites have a high capacity for the degradation of formaldehyde in the vapour phase.

36 MATERIALS SCIENCE↗

DOE OSTI2018

Recovery of Chromium(III) from Tannery Wastewater by Nanoparticles and Whiskers of Chitosan

Chitosan, its nanoparticles and whiskers present an excellent capacity to complex chromium ions. However, this phenomenon is influenced by different parameters. In our search, we determined the appropriate range of pH to form chitosan–Cr(III), nanoparticles Cr(III) and whiskers–Cr(III) complex. We studied also the influence of chromium concentration and nature of chitosan-based materials on complexation process. Our main aim is approximate the optimal conditions to remove chromium(III) from tanning bath, recuperated from tannery wastewater of Marrakech in Morocco. However, the results of adsorption kinetic in tannery wastewater revealed that chitosan, its nanoparticles, whiskers and biocomposites are good sorbent of chromium as well, even if the adsorbed quantity is less compared to chromium solution. Although, according to ICP-OES analysis in this real effluent, nanoparticles are the best complexing ligand, after 24 h of contact nanoparticles can remove 70% of chromium from this tannery wastewater.

54 ENVIRONMENTAL SCIENCES↗

DOE OSTI2018

Mechanical, Barrier and Antioxidant Properties of Chitosan Films Incorporating Cinnamaldehyde

Chitosan films (CF) [1 and 2% w/v] alone and with cinnamaldehyde (CNE) [0.25, 0.5 and 1% v/v] were prepared using an emulsion method, and the obtained films were characterized in terms of water vapor permeability (WVP), water solubility and optical, mechanical and antioxidant properties. The incorporation of CNE at 1% (v/v) significantly decreased the water solubility of the film by approximately 4% for the 1 and 2% CF films, whereas the WVP increased (2.5–3.5 times). The incorporation of CNE (0.25 and 0.5%) into 2% CF significantly increased the tensile strength (TS) (62 and 34%, respectively) and the percent elongation (%E) values, 26, 30 and 52% for CF that contained 0.25, 0.5 and 1% CNE, respectively. The largest value of the elasticity modulus (EM) was observed for 2% CF with 0.25% CNE. All films exhibited a yellow appearance (b*), but the CNE content had a marked impact on the coloration of the films. The CNE recoveries of the CF films (1 and 2%) with 1% of CNE were high (43 and 67%). The antioxidant activities indicated that the incorporation of 1% CNE into CF films (1 and 2%) increased the antioxidant activity. The protective effects of the films with and without CNE on erythrocytes were very strong (36–72% hemolysis inhibition). These results suggest there are potential applications for CF-CNE films as active packaging for the preservation of food products.

36 MATERIALS SCIENCE↗

DOE OSTI2018

Exploration of the Effect of Chitosan and Crosslinking Agent Concentration on the Properties of Dual Responsive Chitosan-g-Poly (N-Isopropylacrylamide) Co-polymeric Particles

The objective of the present study was to synthesize and evaluate the effect of change in concentration of chitosan (CS) and N,N-methylenebisacrylamide (MBA)- a cross linking agent, on various properties such as lower critical solution temperature (LCST), zeta potential, particle size and poly dispersity index (PDI) of the synthesized co-polymer. Nine different formulations of chitosan-g-poly (N-isopropylacrylamide) (CS-g-PNIPAAm) co-polymer with varying CS and MBA concentrations were synthesized by a surfactant free dispersion copolymerization method. The synthesized co-polymer was further characterized and confirmed for its structure, morphology, particle size, zeta-potential, thermo and pH responsive properties, in-vitro cyto-compatability and stability studies using various analytical tools. The data confirms the successful synthesis of co-polymer. The increase in the concentrations of CS and MBA during the polymerization of co-polymer, resulted in proportional increase of LCST and zeta potential with decrease in particle size of co-polymeric nanoparticles. pH responsive studies showed that as the pH of the medium increases particle size and zeta potential decreases with increase in LCST of co-polymeric nanoparticles. From the results, it can be inferred that the synthesized co-polymeric nanoparticles exerted thermo and pH responsive properties with biocompatibility. By varying the CS and MBA concentrations in the co-polymer, desired LCST, particle size and zeta potential for co-polymeric nanoparticles can be obtained and thus the synthesized co-polymer may have great potential to be used as a drug carrier (nanoform) with both thermo and pH responsiveness.

36 MATERIALS SCIENCE↗

DOE OSTI2018

Synthesis of CS/PVA Biodegradable Composite Nanofibers as a Microporous Material with Well Controllable Procedure Through Electrospinning

In this study, we have showed a facile route for fabrication of a novel microporous material based on chitosan (CS) and poly(vinyl alcohol) (PVA) biodegradable nanofibers that have high specific surface area, considerable porosity, and small diameter. Scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, fourier transform infrared spectroscopy, Brunauer–Emmett–Teller surface area analysis, and CHNS/O elemental analyser were applied to characterize the fabricated CS/PVA composite nanofibers. Moreover, the influences of spinning conditions including concentration, voltage, electrospinning distance, and flow rate, on size distribution and pore diameter of the final product were systematically studied using 2{sup k−1} factorial design experiments, and the response surface optimization was used for determining the best synthesis parameter. The results obtained from 2{sup K−1} factorial design experiments showed that electrospinning parameters influenced the size distribution and pore diameter of the CS/PVA microporous material. Based on the response surface methodology, the CS/PVA product could be obtained with a high microporous diameter of 1.8 nm and a small diameter distribution of 15.0 nm under optimized conditions. The obtained results showed that the fabricated samples could be utilized in different applications.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

DOE OSTI2018

Synthesis of N-Guanidinium-Chitosan/Silica Hybrid Composites: Efficient Adsorbents for Anionic Pollutants

A new chitosan derivative, N-guanidinium chitosan acetate, has been synthesized by direct guanylation of chitosan by cyanamide in presence of scandium(III) triflate under mild acidic condition. Starting from this material, N-guanidinium chitosan/silica microhybrids were prepared via a sol gel method using 3-glycidoxypropyl trimethoxysilane as silica precursor. Both N-guanidinium chitosan and the N-guanidinium chitosan/silica hybrid were characterized by a range of analytical techniques such as {sup 29}Si/{sup 13}C solid state NMR, FT-IR, scanning electron microscopy, thermogravimetry and elemental analysis. The characterization of the chitosan/silica hybrid indicated that this material is a highly hydrophilic nanocomposite material containing an organic core and a highly condensed silica shell. The N-guanidinium chitosan/silica microhybrids display excellent adsorption properties for anionic dyes such as methyl orange (MO) with very high capacities up to 917 mg/g. The fixation of MO as anionic dye was investigated in detail as a function of contact time, pH and the MO concentration. The adsorption kinetics of MO on N-guanidinium chitosan/silica microhybrids was more accurately described by pseudo second-order model. Langmuir isotherm model exhibited a better fit with adsorption data than Freundlich isotherm model. This work opens new possibilities for using N-guanidinium chitosan as a reusable adsorbent for water purification. Graphical Abstract: .

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

DOE OSTI2018

Fabrication of Polypyrrole/Chitosan Nanocomposite Aerogel Monolith for Removal of Cr(VI)

Three-dimensional polypyrrole/chitosan nanocomposite monoliths are fabricated by polymerization of pyrrole in chitosan aqueous solution. The static polymerization of pyrrole monomer and the cross-linking of chitosan by glutaraldehyde occur simultaneously, resulting in the self-assembly of polypyrrole/chitosan nanocomposite aerogel monolith. The addition of methyl orange and glutaraldehyde and the static reaction play key roles in the formation of the self-standing aerogel monolith. The as-prepared monolith with larger specific surface area exhibits much better adsorption capability for Cr(VI) removal in comparison with that prepared without the addition of glutaraldehyde. The adsorption process and adsorption isotherms are found to well follow the pseudo-second-order and Langmuir models, respectively. Furthermore, this polypyrrole/chitosan nanocomposite monolith is stable and recyclable. About 73.5% of the initial adsorption capability is kept after eight adsorption–desorption cycles. The polypyrrole/chitosan nanocomposite monolith can be a promising candidate for the efficient removal of Cr(VI).

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗

DOE OSTI2018

Boron Removal by Adsorption on Cobalt(II) Doped Chitosan Bio-composite

Cobalt(II) doped chitosan bio-composite was prepared, characterized and used to oxoborate separation from aqueous solutions. The adsorption process was carried out in a batch system. The effect of pH, temperature, time and initial boron concentration on the boron adsorption were tested. The maximum boron adsorption was reached at pH range 8.0–8.5 at room temperature and within 60 min. Calculations based on Langmuir and Freundlich models showed the heterogeneous nature of boron adsorption on Co-CTS bio-composite. On the base of research on optimization of pH and results from XRD and FTIR analysis it was found that boron adsorption by Co-CTS occurred through the co-precipitation and adsorption of B on cobalt hydroxide following the Coulomb attraction of B(OH){sub 4}{sup −} species on positively charged sites and molecular attraction of H{sub 3}BO{sub 3} through hydrogen bond with amine or hydroxyl groups of chitosan. The modelling of the thermodynamic data indicated the nonspontaneous and exothermic nature of the adsorption process. The pseudo-second-order model adequately described the boron adsorption on Co-CTS hydrogel. Desorption by means of alkaline solution at pH 12 was carried out successfully. Adsorption–desorption efficiencies in 3 cycles were almost 100%.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

DOE OSTI2018

Utilization of a Novel Chitosan/Clay/Biochar Nanobiocomposite for Immobilization of Heavy Metals in Acid Soil Environment

An organic–inorganic composite of chitosan, nanoclay, and biochar (named as MTCB) was chosen to develop a bionanocomposite to simultaneously immobilize Cu, Pb, and Zn metal ions within the contaminated soil and water environments. The composite material was structurally and chemically characterized with the XRD, TEM, SEM, BET, and FT-IR techniques. XRD and TEM results revealed that a mixed exfoliated/intercalated morphology was formed upon addition of small amounts of nanoclay (5% by weight). Batch adsorption experiments showed that the adsorption capacity of MTCB for Cu{sup 2+}, Pb{sup 2+}, and Zn{sup 2+} were much higher than that of the pristine biochar sample (121.5, 336, and 134.6 mg g{sup −1} for Cu{sup 2+}, Pb{sup 2+}, and Zn{sup 2+}, respectively). The adsorption isotherm for Cu{sup 2+} and Zn{sup 2+} fitted satisfactorily to a Freundlich model while the isotherm of Pb{sup 2+} was best represented by a Temkin model. That the adsorption capacity increased with increasing temperature is indicative of the endothermic nature of the adsorption process. According to the FTIR analysis, the main mechanism involved in immobilization of metals is binding with –NH{sub 2} groups. Results from this study indicated that modification of biochar by chitosan/clay nanocomposite enhances its potential capacity for immobilization of heavy metals, rendering the bionanocomposite into an efficient heavy metal sorbent in mine-impacted acidic waters and soils.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

DOE OSTI2018

Modelling and Optimization of Uranium (VI) Ions Adsorption Onto Nano-ZnO/Chitosan Bio-composite Beads with Response Surface Methodology (RSM)

Nano-ZnO-chitosan bio-composite beads were prepared for the sorption of UO{sub 2}{sup 2+} from aqueous media. The resulting nano-ZnO/CTS bio-composite beads were characterized by TEM, XRD etc. The sorption of UO{sub 2}{sup 2+} by bio-composite beads was optimized using RSM. The correlation between four variables was modelled and studied. According to RSM data, correlation coefficients (R{sup 2} = 0.99) and probability F-values (F = 2.24 × 10{sup − 10}) show that the model fits the experimental data well. Adsorption capacity for nano-ZnO/CTS bio-composite beads was obtained at 148.7 mg/g under optimum conditions. The results indicate that nano-ZnO/CTS bio-composite beads are appropriate for the adsorption of UO{sub 2}{sup 2+} ions from aqueous media. Also, the suitability of adsorption values to adsorption isotherms was researched and thermodynamic data were calculated.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

DOE OSTI2018

Development of Chitosan Membranes as a Potential PEMFC Electrolyte

Commercial chitosan and chitosan extracted from shrimp shells are being used to design membranes to be tested as low cost electrolyte in PEM fuel cells. This study investigated the influence of the deacetylation degree (DD) and molar mass (M{sub V}) of the chitosans used in the composition of membranes on its performance regarding to proton conductivity and other properties. Preliminary results indicate that the chitosan extracted from shrimp shells generated membranes with promising properties such as proton conductivity, which demonstrated to be even a 100 times higher than those shown by commercial chitosan membranes. The significant increase in proton conductivity can be associated with the higher number and availability of amino groups (–NH{sub 2}) in the chitosan produced in the laboratory, which presents higher DD and lower M{sub V}. It is believed that the properties of chitosan can be manipulated in such a way that it would be possible to obtain proton conductivity values closer to that presented by Nafion{sup ®}.

30 DIRECT ENERGY CONVERSION↗

DOE OSTI2018

Influence of Glutaraldehyde Crosslinking and Alkaline Post-treatment on the Properties of Chitosan-Based Films

Depending on the modifications proposed, chitosan films present different characteristics, for instance correlated to hydrophilicity, chemical and mechanical properties. The aim of this study was to evaluate the influence of glutaraldehyde crosslinking and an alkaline post-treatment with NaOH on the characteristics of chitosan based films. Films were obtained by casting and characterized by thickness, swelling degree, mechanical and thermal properties and chemical structure. The water vapor permeability (WVP) was also evaluated for food packaging application. It was observed that crosslinking and NaOH post-treatment have great influence on the chitosan films characteristics. Crosslinking reduced the swelling degree of films and increased its fragility, whereas NaOH treatment also reduces the swelling degree and changes mechanical properties, acting in the same way as a crosslinker. The WVP analyses showed that the basic treatment could substitute the glutaraldehyde crosslinking for film water stability, without greatly compromising the barrier properties of chitosan based films.

36 MATERIALS SCIENCE↗

DOE OSTI2018

Preparation, Characterization and Dye Adsorption/Reuse of Chitosan-Vanadate Films

Chitosan used on dyes adsorption when in film form shows limitations due to its low regeneration capacity. In this work, chitosan films were modified using vanadium ions to improve its regeneration capacity on the dye adsorption. Films were characterized and analyzed by FT-IR, XRD and DSC. Adsorption assays were performed using chitosan-vanadate films (CVF) to remove the Reactive Black 5 dye in aqueous solution. The adsorption was favored by the pH decrease from 8.0 to 4.0. The equilibrium data were best fitted by Langmuir model, with q{sub m} of 522 mg g{sup −1} at 298 K. The negative value of ΔH{sup 0} (−9.91 kJ mol{sup −1}) showed an exothermic operation and the value of ΔS{sup 0} was positive (0.0705 kJ mol{sup −1} K{sup −1}), suggesting an increase in randomness at the solid/solution interface. The kinetics was represented by pseudo-first order model and around 80 min occurred a reduction in the adsorption rates, due to the mass transfer mechanism. The most appropriate eluent to remove the RB5 from CVF was NH{sub 4}OH 0.01 kg mol L{sup −1}. The CVF used to the dye adsorption were regenerated and reutilized five times, and the adsorption capacity was around 80% of the initial value after the last cycle.

36 MATERIALS SCIENCE↗

DOE OSTI2018

Effect of Gamma Radiation on the Properties of Crosslinked Chitosan Nano-composite Film

Chitosan nano-composite film crosslinked by citric acid and with glycerol as plasticizer and MgO as antibacterial agent was prepared by casting method. MgO nanoparticles were synthesized via calcination method in furnace at 500 °C for 4 h and characterized by X-ray diffraction and transmission electron microscope. The chitosan nano-composite film with composition chitosan/citric/glycerol/magnesium oxide (1 wt%:1 wt%:75 vol%:10 wt%) has high mechanical properties than other films. The effects of different irradiation doses on the mechanical, thermal and antibacterial activity were investigated. The tensile strength enhanced by increasing irradiation dose up to 10 kGy and the elongation negligible changed as irradiation dose increased. The thermal stability slightly increased up to dose 2.5 kGy then decreased with dose increment. The antimicrobial activity film was studied against white mulberry-borne bacterial pathogens either Gram positive or Gram negative bacteria and has positive impact of gamma irradiation on the antimicrobial activity. The use of the selected chitosan nano-composite film which irradiated by dose of 2.5 kGy and has magnesium oxide of average particle size 54.3 nm as new packaging materials found to improve storage quality and shelf-life of mulberry fruit.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

DOE OSTI2018

Towards Synthesis, Characterization and Properties of Smart Material Based on Chitosan Using Mn-IV Itaconic Acid as a Novel Redox Pair

The precipitation technique of Mn-IV/itaconic acid redox pair was chosen for grafting meth acrylic acid onto chitosan. This was done to maximize the graft yield and minimize the homopolymer formation to lower extent in addition to prepare water soluble chitosan instead of non-eco friendly acid soluble one. Evidence of grafting was confirmed instrumentally by (FTIR, SEM, and TGA), titrimetrically using carboxyl content and gravimetrically using dry weight method. The mechanism of grafting and factors affected grafting reaction were studied in details, and the optimum reaction conditions were obtained at [chitosan] 2 g, [MnO{sub 2}] 25.9 mmol/100 g sample, [itaconic acid],100 mmol/L, [MAA] 50% bows,[liquor ratio], 25, reaction time, 2 h, and [reaction temperature], 65 °C. It is also seen from the obtained results that, the resultant copolymer showed the following findings: (a) only nitric acid solutions are proved to be a superior solvent for the grafted product; (b) superabsorbent towards water (197 g H{sub 2}O/g polymer) and saline absorbency (60 g saline solution/g polymer) after cross-linked with epichlorohydrin, (c) higher water solubility (21%) at 48% graft yield and (d) 73.5% copper ion removal in comparison with 41% for chitosan.

36 MATERIALS SCIENCE↗

DOE OSTI2018

Properties of Poly(Vinyl Alcohol)/Chitosan Nanocomposite Films Reinforced with Oil Palm Empty Fruit Bunch Amorphous Lignocellulose Nanofibers

The objective of this study was to investigate the properties of poly(vinyl alcohol)/chitosan nanocomposite films reinforced with different concentration of amorphous LCNFs. The properties analyzed were morphological, physical, chemical, thermal, biological, and mechanical characteristics. Oil palm empty fruit bunch LCNFs obtained from multi-mechanical stages were more dominated by amorphous region than crystalline part. Varied film thickness, swelling degree, and transparency of PVA/chitosan nanocomposite films reinforced with amorphous part were produced. Aggregated LCNFs, which reinforced PVA/chitosan polymer blends, resulted in irregular, rough, and uneven external surfaces as well as protrusions. Based on XRD analysis, there were two or three imperative peaks that indicated the presence of crystalline states. The increase in LCNFs concentration above 0.5% to PVA/chitosan polymer blends led to the decrease in crystallinity index of the films. A noticeable alteration of FTIR spectra, which included wavenumber and intensity, was obviously observed along with the inclusion of amorphous LCNFs. That indicated that a good miscibility between amorphous LCNFs and PVA/chitosan polymer blend generated chemical interaction of those polymers during physical blending. Reinforcement of PVA/chitosan polymer blends with amorphous LCNFs influenced the changes of T{sub g} (glass transition temperature), T{sub m} (melting point temperature), and T{sub max} (maximum degradation temperature). Three thermal phases of PVA/chitosan/LCNFs nanocomposite films were also observed, including absorbed moisture evaporation, PVA and chitosan polymer backbone structural degradation and LCNFs pyrolysis, and by-products degradation of these polymers. The addition of LCNFs 0.5% had the highest tensile strength and the addition of LCNFs above 0.5% decreased the strength. The incorporation of OPEFB LCNFs did not show anti-microbial and anti-fungal properties of the films. The addition of amorphous LCNFs 0.5% into PVA/chitosan polymer blends resulted in regular and smooth external surfaces, enhanced tensile strength, increased crystallinity index, and enhanced thermal stability of the films.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

DOE OSTI2018

Kinetic, Isotherm and Thermodynamic Studies for Removal of Methylene Blue Using β-Cyclodextrin/Activated Carbon Aerogels

A novel aerogel (β-CD/AC) was prepared through polymerization reaction of β-cyclodextrin (β-CD) with activated carbon (AC) and vacuum freeze drying method. The structure and morphology of β-CD/AC were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, Brunauer–Emmett–Teller (BET) method and thermogravimetric analysis (TGA). β-CD/AC is used to deal with wastewater containing methylene blue (MB) dye. The effects of AC content in β-CD/AC, pH value, temperature, contact time and amount of adsorbent on the adsorption of MB were studied in detail. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms. The Langmuir monolayer adsorption capacity of MB onto β-CD/AC was estimated as 166.67 mg/g. The kinetics of MB onto β-CD/AC was well described by the pseudo-second order model. The thermodynamic parameters indicated that the adsorption reaction of MB onto β-CD/AC was endothermic and spontaneous.

36 MATERIALS SCIENCE↗