Efficient capture of eosin yellow and crystal violet with high performance xanthan-acacia hybrid super-adsorbent optimized using response surface methodology.

Blending of xanthan and acacia gives a unique hybrid that was used for the synthesis of semi-interpenetrating network (semi-IPN) in which poly(acrylamide) chains were grafted onto hybrid of xanthan-acacia followed by their cross-linking (Xan-Aca-cl-poly(AAm)). Optimization was carried out under response surface methodology-central composite design (RSM-CCD). Maximum percentage swelling of semi-IPN obtained was 496.57%. The concentrations of acrylamide, citric acid and ammonium persulphate used as monomer, cross-linker and initiator, respectively were found to be significant parameters. The blend was highly effective in removal of both cationic (crystal violet) and anionic dyes (eosin yellow) showing maximum dye removal capacity of 97.58% and 95.42%, respectively under optimized parameters - 0.4 g semi-IPN dose in 15 ml dye solution of 10 mg L-1 concentration within 16 h. Adsorption mechanism of both the dyes followed three steps in accordance with intraparticle diffusion model along with mono layer langmuir adsorption criteria. Second order kinetics was followed in case of both dyes. Thermodynamic studies gave idea about the exothermic nature of adsorption. Semi-IPN could be recycled up to eight consecutive cycles and hence, can be utilized for industrial purpose for removal of dyes.

Selective removal of cationic dyes using response surface methodology optimized gum acacia-sodium alginate blended superadsorbent.

Gum acacia and sodium alginate were blended to synthesize highly efficient superadsorbent formed by grafting of poly(acrylic acid) (AA) used as monomer onto the hybrid of gum acacia and sodium alginate and the polymeric chains were crosslinked through N,N'-methylene bisacrylamide (MBA). The overall reaction followed free radical polymerization with ammonium persulphate (APS) used as initiator. Response surface methodology integrated with central composite design (RSM-CCD) could synthesize semi-Interpenetrating network (semi-IPN) having maximum swelling capacity of 1749.2% at MBA, APS and AA concentrations of 0.89 × 10-2 mol L-1, 3.29 × 10-2 mol L-1 and 1.46 mol L-1, respectively using 15 mL water at 70 °C for 2.5 h. The synthesized sample was found to be selective for removal of cationic dyes upto 97.49%, 95.39% and 94.56% for auramine-O (AO), malachite green (MG) and crystal violet (CV), respectively. Adsorption capacities at equilibrium were calculated experimentally as 2.01 mg g-1, 3.06 mg g-1 and 7.55 mg g-1 for AO, MG and CV, respectively. These dyes could be desorbed with 0.1 N HCl for the recyclization of semi-IPN. Adsorption mechanism involved monolayer formation with three step process of adsorption and followed first order kinetics. Exothermic nature of adsorption was revealed by thermodynamic studies.

Response surface methodology directed synthesis of luminescent nanocomposite hydrogel for trapping anionic dyes.

The present research work reveals semi-interpenetrating network (semi-IPN) synthesis using response surface methodology-central composite design (RSM-CCD) based optimization. The maximum swelling of 362.11% was obtained with monomer, crosslinker and initiator concentrations 4.39 mol L-1, 1.52 mol L-1 and 4.58 mol L-1, respectively, temperature 70 °C, time 3 h and pH 4.0. The synthesized hydrogel showed 94.16% and 95.62% removal for eosin yellow (EY) and eriochrome black-T (EBT) dyes, respectively. The incorporation of cadmium sulphide nanodots into the hydrogel network enhanced the % dye removal (96.82% EY and 98.73% EBT) along with fluorescent behavior. Various conditions optimized for EY and EBT dye removal with respect to semi-IPN were: 0.4 g adsorbent dose each, dye concentrations 10 mg L-1 and 120 mg L-1, contact time 24 h each, respectively. Adsorption studies followed langmuir theory for both dyes. Second order and first order kinetics along with intraparticle diffusion of dye molecules were favorable to EY and EBT, respectively. Thermodynamic study reveals exothermic nature of adsorption. Recyclability of the adsorbent is superior as tested by desorption-adsorption tests.