New Thermal and Microbial Resistant Metal-Containing Epoxy Polymers

A series of metal-containing epoxy polymers have been synthesized by the condensation of epichlorohydrin (1-chloro-2,3-epoxy propane) with Schiff base metal complexes in alkaline medium. Schiff base was initially prepared by the reaction of 2,6 dihydroxy 1-napthaldehyde and o-phenylenediamine in 1  :  2 molar ratio and then with metal acetate. All the synthesized compounds were characterized by elemental, spectral, and thermal analysis. The physicochemical properties, viz., epoxy value, hydroxyl content, and chlorine content [mol/100 g] were measured by standard procedures. The antimicrobial activities of these metal-containing epoxy polymers were carried out by using minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) methods against S. aureus, B. subtilis (Gram-positive bacteria), and E. coli, P. aeruginosa (Gram-negative bacteria). It was found that the ECu(II) showed higher antibacterial activity than other metal-chelated epoxy resin while EMn(II) exhibited reduced antibacterial activity against all bacteria

Metal-Containing Epoxy Polymers

A series of metal-containing epoxy polymers have been synthesized by the condensation of epichlorohydrin (1-chloro-2,3-epoxy propane) with Schiff base metal complexes in alkaline medium. Schiff base was initially prepared by the reaction of 2,6 dihydroxy 1-napthaldehyde and o-phenylenediamine in 1 : 2 molar ratio and then with metal acetate. All the synthesized compounds were characterized by elemental, spectral, and thermal analysis. The physicochemical properties, viz., epoxy value, hydroxyl content, and chlorine content [mol/100 g] were measured by standard procedures. The antimicrobial activities of these metal-containing epoxy polymers were carried out by using minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) methods against S. aureus, B. subtilis (Gram-positive bacteria), and E. coli, P. aeruginosa (Gram-negative bacteria). It was found that the ECu(II) showed higher antibacterial activity than other metal-chelated epoxy resin while EMn(II) exhibited reduced antibacterial activity against all bacteria

Semibath Polymerization Approach for One-Pot Synthesis of Temperature- and Glucose-Responsive Core-Shell Nanogel Particles

Herein, we report a simple and easy procedure for the synthesis of core-shell structures of glucose-sensitive 3-acrylamidophenylboronic acid (APBA) and temperature-responsive P(NIPAm-AAc) shell nanogel particles using MBA as a cross-linker via free radical polymerization. The synthesized particles were approximately 100 nm and were cross-linked to one another. The shell thickness of the nanogel particles was adjusted by increasing the concentrations of NIPAm through the semibath approach during the process of polymerization. The synthesized colloidal nanogel particle shows thermoresponsive behaviors. The dynamic light scattering technique also confirmed the change in the size of particles dispersed in an aqueous solution upon increase/decrease in temperatures, which is the result of its volume phase transition temperatures (VPTT). The size and morphology of the particles were characterized by TEM, FE-SEM, and AFM. The sensitivity of these nanogel particles to temperature and glucose suggests that they have the potential for applications related to the delivery of self-regulated insulin

Coordination Polymer: Synthesis, Spectral Characterization and Thermal Behaviour of Starch-Urea Based Biodegradable Polymer and Its Polymer Metal Complexes

A starch-urea-based biodegradable coordination polymer modified by transition metal Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) was prepared by polycondensation of starch and urea. All the synthesized polymeric compounds were characterized by Fourier transform-infrared spectroscopy (FT-IR), (1)H-NMR spectroscopy, (13)C-NMR spectroscopy, UV-visible spectra, magnetic moment measurements, differential scanning calorimeter (DSC), and thermogravimetric analysis (TGA). The results of electronic spectra and magnetic moment measurements indicate that Mn(II), Co(II), and Ni(II) complexes show octahedral geometry, while Cu(II) and Zn(II) complexes show square planar and tetrahedral geometry, respectively. The thermogravimetric analysis revealed that all the polymeric metal complexes are more thermally stable than the parental ligand. In addition, biodegradable studies of all the polymeric compounds were also carried out through ASTM standards of biodegradable polymers by CO(2) evolution method

Bimetallic metal-organic frameworks for controlled catalytic graphitization of nanoporous carbons

Single metal-organic frameworks (MOFs), constructed from the coordination between one-fold metal ions and organic linkers, show limited functionalities when used as precursors for nanoporous carbon materials. Herein, we propose to merge the advantages of zinc and cobalt metals ions into one single MOF crystal (i.e., bimetallic MOFs). The organic linkers that coordinate with cobalt ions tend to yield graphitic carbons after carbonization, unlike those bridging with zinc ions, due to the controlled catalytic graphitization by the cobalt nanoparticles. In this work, we demonstrate a feasible method to achieve nanoporous carbon materials with tailored properties, including specific surface area, pore size distribution, degree of graphitization, and content of heteroatoms. The bimetallic-MOF-derived nanoporous carbon are systematically characterized, highlighting the importance of precisely controlling the properties of the carbon materials. This can be done by finely tuning the components in the bimetallic MOF precursors, and thus designing optimal carbon materials for specific applications

Structural and electrochemical studies of proton conducting biopolymer blend electrolytes based on MC:Dextran for EDLC device application with high energy density

This study shows preparation and characterization of solid biopolymer electrolyte based on glycerolized methylcellulose (MC): dextran-doped with ammonium thiocyanate (NH4SCN). The nature of electrolyte composition in terms of interaction is characterized using Fourier transform infrared (FTIR) technique. Lowering and shifting in the intensity of the bands are observed with increasing the quantity of glycerol as a plasticizer, confirming complexation between electrolyte components. Ion transport parameters are determined using both of the methods of EIS and FTIR where the parameters are found to be increased with glycerol concentration. The transport number measurement indicates that ions are the primary charge carrier in the conduction mechanism where tion is found to be 0.961. The maximum DC ionic conductivity value is achieved that found to be 1.63 � 10�3 S cm�1. The ESR values are ranged from 300 to 580 O throughout 450 cycles. The technique of linear sweep voltammetry (LSV) shows the electrochemical stability window of 2 V for the conducting samples. The response of cyclic voltammetry (CV) shows an almost rectangular shape without Faradaic peaks. A galvanostatic charge–discharge investigation has shown the initial specific capacitance, energy density, and power density are 133 F g�1, 18.3 Wh Kg�1, and 680 W Kg�1, respectively

Jute-derived microporous/mesoporous carbon with ultra-high surface area using a chemical activation process

Here, we report the synthesis of nanoporous carbons (NCs) derived from a low-cost and renewable biomass, jute, by a chemical activation process using KOH. Jute is one of the least expensive and most abundant crops, with a staggering 2.8 million metric tons of jute produced each year. In this study, we synthesize NCs from three different parts of jute fibers through a chemical activation technique using KOH. The NCs prepared from the bottom portion of the fiber show a high surface area (2682 m g) with the presence of both micropores and mesopores. The ultra-high surface area of jute makes it an economically viable, environmentally friendly precursor for NCs, with a wide variety of applications from energy storage to environmental and biomedical applications

Fabrication of Highly Porous Polymeric Nanocomposite for the Removal of Radioactive U(VI) and Eu(III) Ions from Aqueous Solution

In the present study, a polymeric nanocomposite, CoFe2O4@DHBF, was fabricated using 2,4 dihydroxybenzaldehyde and formaldehyde in basic medium with CoFe2O4 nanoparticles. The fabricated nanocomposite was characterized using FTIR, TGA, XRD, SEM, TEM, and XPS analyses. The analytical results revealed that the magnetic nanocomposite was fabricated successfully with high surface area 370.24 m2/g. The fabricated CoFe2O4@DHBF was used as an efficient adsorbent for the adsorption of U(VI) and Eu(III) ions from contaminated water. pH, initial concentration, adsorption time, and the temperature of the contaminated water solution affecting the adsorption ability of the nanocomposites were studied. The batch adsorption results exposed that the adsorption capacity for the removal of U(VI) and Eu(III) was found to be 237.5 and 225.5 mg/g. The adsorption kinetics support that both the metal ions follow second order adsorption kinetics. The adsorption isotherm well fits with the Langmuir adsorption isotherm and the correlation coefficient (R2) values were found to be 0.9920 and 0.9913 for the adsorption of U(VI) and Eu(III), respectively. It was noticed that the fabricated nanocomposites show excellent regeneration ability and about 220.1 and 211.3 mg/g adsorption capacity remains with U(VI) and Eu(III) under optimum conditions