Biocompatible carboxymethyl chitosan-modified glass ionomer cement with enhanced mechanical and anti-bacterial properties.

Due to the potential adverse effects of conventional dental cements, the demand for biocompatible cements have grown tremendously in the field of dentistry. In this respect, Glass ionomer cements (GICs) are being developed by different researchers. However, low mechanical strength of GIC make them unsuitable for application in high-stress areas. Thus, numerous initiatives to improve mechanical performance have been attempted till date including incorporation of reinforcing fillers. Novelty of the study lies in using carboxymethyl chitosan (CMC) to develop a biocompatible dental cement (DC/CMC-m-GP), which would have enhanced mechanical strength due to greater interaction of CMC with the particles of GIC and better cyto-compatibility due to its cell-proliferation activity. The mechanical strength, acid erosion and fluoride release of DC/CMC-m-GP were studied and compared with control dental cement (DC/Control). DC/CMC-m-GP shows compressive strength of 157.45 M Pa and flexural strength of 18.76 M Pa which was higher as compared to DC/Control. The morphology of the GICs were studied through FESEM. Anti-microbial activity of DC/CMC-m-GP was studied by Agar disc-diffusion method and biofilm assay against S. mutans, which shows that DC/CMC-m-GP inhibits bacterial adhesion on its surface. MTT assay infers that DC/CMC-m-GP was non-cytotoxic and did not affect the cell viability significantly.

Plasma polymerized functional supermagnetic Fe3O4 nanostructured templates for laccase immobilization: A robust catalytic system for bio-inspired dye degradation.

Fe3O4 magnetic nanoparticles, synthesized using co-precipitation method, were epoxy functionalized via plasma polymerization of 2,3-epoxypropylmethacrylate (EPMA) precursor. The EPMA-functionalized Fe3O4 nanoparticles (EPMA-f-MN) were employed as templates for facile, one-step covalent immobilization of laccase enzyme at room temperature. Samples were rigorously characterized by FTIR, TGA, SEM, TEM, XRD techniques, while Mössbauer spectroscopy (MöS) and vibrating sample magnetometry (VSM) confirmed the supermagnetic nature of Fe3O4 nanoparticles. Activities of free and immobilized laccase (ImLac) were assayed by spectrophotometrically monitoring the enzymatic reduction of substrate 2,2-azino-bis(3-ethylthiazoline-6-sulfonate) (ABTS) at 420 nm, corresponding to the λmax of ABTS.+. In addition to possessing higher thermal stability and a broader pH tolerance window compared to free laccase, the supermagnetic property of the Fe3O4 renders the ImLac system conveniently recoverable and recyclable. Practical applicability of ImLac towards catalytic degradation of industrial dyes was also ably demonstrated using Acid Blue 193 (AB 193) as a commercially used model textile dye, which belongs to the family of azo dyes. Over 95% degradation of the dye was achieved within a period of 4 hours. ImLac could be used for more than 10 dye degradation cycles with >90 % of retention in enzyme activity.

Radiation grafted cellulose fabric as reusable anionic adsorbent: A novel strategy for potential large-scale dye wastewater remediation.

A low cost, cellulose based anionic adsorbent has been synthesized at room temperature by single step gamma radiation induced grafting of 4-vinylbenzenesulfonic acid sodium salt (VBSA) onto cellulose using water as solvent. Grafting parameters, namely, radiation dose, monomer concentration, volume/weight ratio, were studied to optimize the radiation grafting process. Poly(VBSA) grafted cellulose (PVBSA-g-cellulose) samples were characterized by grafting yield estimation, Elemental analysis, FTIR, TGA and SEM. The radiation grafted adsorbent was tested for textile dyes removal from aqueous solutions, in batch and continuous flow column operation mode, using Basic Red-29 (BR-29) dye as a model textile dye. Adsorbent with 25% grafting yield exhibited an adsorption capacity of 320 mg.g-1, which was corroborated by the equilibrium adsorption and kinetic studies. The adsorbent was regenerated and demonstrated to be reusable for multiple cycles with minimal attrition losses. The process was successfully upscaled and demonstrated at a semi pilot scale treatment.

Mitigation of Cr(VI) toxicity using Pd-nanoparticles immobilized catalytic reactor (Pd-NICaR) fabricated via plasma and gamma radiation.

Catalytic reduction of Cr(VI) to less toxic Cr(III) form using metal nanoparticles is one of the novel approaches adopted to deal with Cr toxicity. In this work, we report the fabrication of a facile, reusable, and robust Pd nanoparticles-immobilized catalytic reactor (Pd-NICaR) system using green, environment-friendly gamma radiolytic, and plasma polymerization processes. A room temperature, RF-powered plasma polymerization process was employed to functionalize a polyethylene-polypropylene (PE-PP) non-woven matrix with epoxy group containing monomer 2,3-epoxypropyl methacrylate (EPMA). EPMA-functionalized PE-PP (EPMA-f-PE-PP) substrate was subsequently used as a template for in situ generation and immobilization of Pd NPs via gamma radiolytic route. The samples were characterized using FTIR, SEM, XPS, and XRF techniques. The catalytic efficacy of Pd-NICaR towards Cr(VI) reduction, in the presence of formic acid (FA) as a reductant, was investigated spectrophotometrically, and reaction parameters were optimized at reaction temperature of 50 °C and [FA]/[Cr(VI)] = 680 to achieve catalytic reduction efficiency of 99.7% within 10 min in batch process. The system showed excellent reusability (~ 20 cycles) and storage stability (> 30 days) without substantial loss (~ 11%) of activity. Practical applicability of the robust catalytic system towards Cr(VI) toxicity mitigation was established in continuous flow mode using a fixed-bed column reactor.

Cellulose based cationic adsorbent fabricated via radiation grafting process for treatment of dyes waste water.

A cationized adsorbent was prepared from cellulosic cotton fabric waste via a single step-green-radiation grafting process using gamma radiation source, wherein poly[2-(methacryloyloxy) ethyl]trimethylammonium chloride (PMAETC) was covalently attached to cotton cellulose substrate. Radiation grafted (PMAETC-g-cellulose) adsorbent was investigated for removal of acid dyes from aqueous solutions using two model dyes: Acid Blue 25 (AB25) and Acid Blue 74 (AB74). The equilibrium adsorption data was analyzed by Langmuir and Freundlich isotherms, whereas kinetic data was analyzed by pseudo first order, pseudo second order, intra particle diffusion and Boyd's models. The PMAETC-g-cellulose adsorbent with 25% grafting yield exhibited equilibrium adsorption capacities of ∼ 540.0mg/g and ∼ 340.0mg/g for AB25 and AB74, respectively. Linear and nonlinear fitting of adsorption data suggested that the equilibrium adsorption process followed Langmuir adsorption isotherm model, whereas, the kinetic adsorption process followed pseudo-second order model. The multi-linearities observed in the intra-particle kinetic plots suggested that the intraparticle diffusion was not the only rate-controlling process in the adsorption of acid dyes on the adsorbent, which was further supported by Boyd's model. The adsorbent could be regenerated by eluting the adsorbed dye from the adsorbent and could be repeatedly used.