Batch adsorption studies on surface tailored chitosan/orange peel hydrogel composite for the removal of Cr(VI) and Cu(II) ions from synthetic wastewater.

Elimination of heavy metals from wastewater has been a significant process to improve the aquatic source's quality. Various materials act as very effective adsorbents to remove heavy metals, which cause toxicity to plants and all other living organisms. Thus, the present work focuses on removing heavy metals chromium (Cr) and copper (Cu) ions containing wastewater using biodegradable and cost-effective chitosan-based hydrogel composite. The composite was prepared via chemical cross-linking of radical chitosan with polyacrylamide and N,N'-Methylene bisacrylamide and blended with orange peel. The synthesis of the adsorbent has been confirmed by using Fourier-transform infrared spectroscopy (FT-IR), Scanning electron microscopy - Energy dispersive X-ray analysis (SEM-EDAX) and X-ray diffraction (XRD) studies. The adsorption power of the composite of metal ions at different time, pH, adsorbent dosages, different metal ion concentrations were analyzed by using Atomic Absorption Spectroscopy (AAS). The results concluded that the optimum pH for Cr(VI) and Cu (II) were 4 and 5, contact time: 360 min, adsorbent dosage: 4 g, and initial metal ion concentration: 100 mg/L for each metal ions. The adsorption isotherm models follow the Freundlich model and pseudo-second-order kinetics. From the results, the adsorption capacity was observed to be 80.43% for Cr(VI) and 82.47% for Cu(II) ions, respectively.

Novel chitosan based thin sheet nanofiltration membrane for rejection of heavy metal chromium.

In recent years, polymeric membranes holds superior position in filtration processes as it was cost effective and simple to prepare. In the present study we have synthesized a novel organic-inorganic hybrid thin sheet membrane using chitosan/polyvinyl alcohol and montmorillonite clay followed by non-solvent induced phase inversion technique. This hybrid clay-polymeric nanofiltration membrane possesses excellent overall performance, such as enhanced hydrophilic nature, and holds good rejection rate. Analytical techniques such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometer (XRD) and Scanning Electron Microscopy (SEM) have been employed to characterize the membrane material. Membrane characterizations such as pure water flux, membrane hydraulic resistance, water content, percentage of porosity and pore size were also evaluated. An important characteristic of membrane for long term usage "anti-biofouling activity" is investigated by determining zone of inhibition of membrane on pathogens of bacterial and fungal strains. The remediation of chromium was performed by varying the parameters such as pH, metal ion concentration, applied pressure and thickness of membrane. The rejection of chromium removal by CS/PVA/MMT membrane is confirmed by comparing the spectral images of EDAX and FT-IR taken before and after filtration.

Banana fiber Cellulose Nano Crystals grafted with butyl acrylate for heavy metal lead (II) removal.

The present work deals with extraction of Cellulose Nano Crystals (CNCs) from Banana fiber using the steam explosion method. Extracted CNCs was grafted with butyl acrylate (BA) monomer with ceric ammonium nitrate (CAN) as an initiator. The prepared graft copolymer was analyzed using FTIR, XRD, SEM and EDAX. FTIR results indicate that the CH2 type of linkages was observed in the grafted copolymer showing effective formation of grafted copolymer. XRD results elucidate the changes in the crystalline behaviour of the prepared CNCs grafted butyl acrylate copolymer. SEM images of a prepared adsorbent was appeared to be heterogeneous and covered with clusters which will be suitable for adsorption. Batch adsorption studies was carried out for the removal of Pb(II) ions from the aqueous solution using the prepared copolymer. The parameters such as effect of pH, contact time, initial metal ion concentration and adsorbent dosage was investigated. From the observed results it was concluded that, the optimum pH: 5, contact time: 360 min, adsorbent dosage: 4 g/100 mL and initial metal ion concentration: 125 mg/L. The adsorption isotherm models of Pb(II) ions could be described very well by Freundlich model and the kinetic results revealed that pseudo-second-order kinetics showed a better fit.

Development of 3D scaffolds using nanochitosan/silk-fibroin/hyaluronic acid biomaterials for tissue engineering applications.

Bone tissue engineering put emphasis on fabrication three-dimensional biodegradable porous scaffolds that supporting bone regeneration and functional bone tissue formation. In the present work, we prepared novel 3D tripolymeric scaffolds of nanochitosan (NCS)/silk fibroin (SF)/hyaluronic acid (HA) ternary blends and demonstrating the synergistic effect of scaffolds and its use in tissue engineering applications. The physico-chemical characterization of the prepared scaffold was evaluated by FTIR, XRD and SEM studies. The FT-IR and XRD results confirmed the interfacial bonding interaction existing between polymers. SEM images showed good interconnected porous structure with rough surface morphology. The in vitro cytocompatibility tests carried out with osteoblast cells by the MTT assay demonstrated that the blended scaffold favors the early adhesion, growth and proliferation of preosteoblast MC3T3-E1 cells. The alizarin red assay indicated that the prepared scaffold can promote the osteogenic differentiation and facilitate the calcium mineralization of MC3T3-E1 cells. The alkaline phosphatase assay confirmed that the NCS/SF/HA scaffold provide conducive environment for osteoblast proliferation and mineral deposition. The bactericidal action of NCS/SF/HA scaffold reveals that the prepared sample has the potential to kill the microorganisms to a greater extent. Hence the overall findings concluded that the NCS/SF/HA scaffolds have better applications in tissue engineering.

Size optimization and in vitro biocompatibility studies of chitosan nanoparticles.

Chitosan (CS), an amino polysaccharide has fascinating scientific applications due to its many flexible properties. The advantages of Chitosan tend to increase when it was modified. Thus, in the present research work, to improve the properties of chitosan, it was converted into chitosan nanoparticles (CS-NPs) through the ionic gelation method using sodium tripoyphosphate (TPP) and sodium hexametaphosphate (SHMP) as a crosslinker. The size optimization was done by varying the parameters such as crosslinker concentration, agitation method and rate, agitation time, temperature and drying method. The prepared samples were characterized using FTIR, TGA, XRD, SEM, TEM and DLS. Also the prepared CS-NPs with TPP and SHMP had been evaluated in vitro for determining its hemocompatibility, biodegradability, serum stability, cytotoxicity and cell viability. The results showed the significant participation of all the parameters in obtaining the nanoparticles in 20-30nm and 5-10nm for CS-NPs-TPP air dried and freeze dried samples and around 60-80nm and 20-30nm for CS-NPs-SHMP air dried and freeze dried samples. The in vitro biological studies revealed that the nanoparticles are non-toxic with a good degree of biodegradability, blood compatibility and stability.

Adsorption Studies of Lead(II) from aqueous solution onto Nanochitosan /Polyurethane /Polypropylene glycol ternary blends.

Chitosan is one of the most abundant natural biopolymer after cellulose. Nanochitosan (NCS) was prepared from chitosan by ionic gelation method with sodium tripolyphosphate. Polyurethanes (PU) find wide range of applications as good materials for the concentration and removal of both organic and inorganic pollutants because of their high efficiency for sorption of various ionic and neutral materials. Polypropylene glycol (PPG) is a family of long chain polymers attached to a glycerine backbone. The present project deals with the aims in exploiting the positive behaviour of the three polymers by preparing a ternary blends of NCS/PU/PPG(1:1:1) ratio. Batch adsorption process was carried out using prepared ternary blend of various parameters influencing the Pb(II) adsorption such as initial concentration of the metal solutions, pH, agitation time and adsorbent concentrations have been studied. The characterization of the prepared sample was carried out using FTIR, XRD, TGA, DSC and SEM studies. Langmuir, Freundlich and Tempkin isotherm parameters have been determined. Adsorption kinetic data were tested using pseudo-first order, pseudo-second order and Elovich model. The kinetics of the adsorption was found to fit the pseudo-second order model. The present work proves the suitability of the ternary blend as an effective adsorbent for Pb(II).

Removal of toxic heavy metal lead (II) using chitosan oligosaccharide-graft-maleic anhydride/polyvinyl alcohol/silk fibroin composite.

The present work was aimed to investigate the efficiency of novel chitosan oligosaccharide-graft-maleic anhydride(COS-g-MAH)/Polyvinyl alcohol (PVA)/silk fibroin (SF) composite for removing the toxic heavy metal lead (II) ion from aqueous solution by batch adsorption studies. Initially the chitosan oligosaccharide-graft-maleic anhydride copolymer has been prepared by utilizing ceric ammonium nitrate as an initiator and the optimised graft copolymer was then used for synthesizing COS-g-MAH/PVA/SF composite. The prepared samples were analyzed through FTIR and XRD studies. The FTIR results indicate that the grafted chitosan oligosaccharide copolymer was mixed homogeneously with silk fibroin and polyvinyl alcohol through intermolecular hydrogen bonding. The XRD results elucidate the changes in the crystalline behaviour of the prepared COS-g-MAH/PVA/silk fibroin composite. Both FTIR and XRD results revealed a strong interaction among COS-g-MAH, PVA and silk fibroin components. To evaluate the adsorption potential of the synthesized composite, the parameters such as pH, adsorbent dosage, contact time and initial Pb(II)ion concentration was investigated. The adsorption isotherms of Pb(II) could be described very well by Langmuir model and the kinetic results revealed that pseudo second order kinetics shows a better fit. This work provides a practical and high-efficient method for water treatment at moderate concentration of toxic heavy metals.

FTIR, XRD and DSC studies of nanochitosan, cellulose acetate and polyethylene glycol blend ultrafiltration membranes.

In the present work, a series of novel nanochitosan/cellulose acetate/polyethylene glycol (NCS/CA/PEG) blend flat sheet membranes were fabricated in different ratios (1:1:1, 1:1:2, 2:1:1, 2:1:2, 1:2:1, 2:2:1) in a polar solvent of N,N'-dimethylformamide (DMF) using the most popular phase inversion method. Nanochitosan was prepared by the ionotropic gelation method and its average particle size has been analyzed using Dynamic Light Scattering (DLS) method. The effect of blending of the three polymers was investigated using FTIR and XRD studies. FTIR results confirmed the formation of well-blended membranes and the XRD analysis revealed enhanced amorphous nature of the membrane ratio 2:1:2. DSC study was conducted to find out the thermal behavior of the blend membranes and the results clearly indicated good thermal stability and single glass transition temperature (Tg) of all the prepared membranes. Asymmetric nature and rough surface morphology was confirmed using SEM analysis. From the results it was evident that the blending of the polymers with higher concentration of nanochitosan can alter the nature of the resulting membranes to a greater extent and thus amorphous membranes were obtained with good miscibility and compatibility.