Strong Antimicrobial Activity of Highly Stable Nanocomposite Containing AgNPs Based on Water-Soluble Triazole-Sulfonate Copolymer

A new hydrophilic polymeric nanocomposite containing AgNPs was synthesized by chemical reduction of metal ions in an aqueous medium in the presence of the copolymer. A new water-soluble copolymer of 1-vinyl-1,2,4-triazole and vinylsulfonic acid sodium salt (poly(VT-co-Na-VSA)) was obtained by free-radical copolymerization and was used as a stabilizing precursor agent. The structural, dimensional, and morphological properties of the nanocomposite were studied by UV–Vis, FTIR, X-ray diffraction, atomic absorption, transmission and scanning electron microscopy, dynamic and electrophoretic light scattering, gel permeation chromatography, thermogravimetric analysis, and differential scanning calorimetry. Hydrodynamic diameter of macroclubs for the copolymer was 171 nm, and for the nanocomposite it was 694 nm. Zeta potential for the copolymer was −63.8 mV, and for the nanocomposite it was −70.4 mV. The nanocomposite had strong antimicrobial activity towards Gram-negative and Gram-positive microorganisms: MIC and MBC values were in the range of 0.25–4.0 and 0.5–8.0 μg/mL, respectively.

Reactivity of 2,3-Dichloropropene in free-radical copolymerization reactions

The copolymers of 2,3-Dichloropropene with vinyl chloride, methyl methacrylate, and styrene of different compositions were obtained via free-radical copolymerization. The copolymerization constants for the comonomers were found from the dependence of the copolymer composition on the initial mixture content. An increase in the content of 2,3-Dichloropropene in the initial mixture was found to decrease the yield and intrinsic viscosity of the copolymer for all systems. The reactivity of 2,3-Dichloropropene in copolymerization reactions was assessed according to the reciprocals of the copolymerization constants of vinyl chloride, methyl methacrylate, and styrene, which indicate the reactivity of the dichlorinated monomer when interacting with comonomer radicals. It was found that 2,3-dichloropropene is the most active in the reaction with a styrene radical. However, its reactivity with a methyl methacrylate radical decreases by a factor of 0.88 as compared to the styrene radical. The lowest reactivity of 2,3-Dichloropropene is observed when interacting with a vinyl chloride radical. The synthesized copolymers can be further modified by replacing chlorine atoms with functional groups.

MB Dye Adsorption Behavior on Poly (N cyclohexylacrylamide-co-Acrylamide/Maleicacid)/ OMMT Nanocomposite Hydrogels

A series of poly (N-cyclohexylacrylamide-co-Acrylamide/Maleic acid) /OMMT nanocomposite hydrogels (NC) were prepared from free-radical copolymerization in water/methanol medium using ammonium persulfate (APS) as a free radical initiator and N,N’- methylene-bis-acryl amide(MBA) as the cross-linker at 60˚C. The nanocomposite hydrogels were synthesized via in situ polymerization using organo modified MMT (O-MMT) nano clay. The optimum swelling of nanocomposite superabsorbents was achieved at 0.150g of OMMT nanoclay. The synthesized nanocomposites were characterized by FTIR, SEM, XRD and TGA techniques. Swelling and diffusion parameters in water and dye solution were calculated. The effect of two cationic salt solutions on the swelling was studied. The hydrogel nanocomposites showed up to 99.9% removal efficiency towards methylene blue dye adsorption study.

Copolymer Involving 2-Hydroxyethyl Methacrylate and 2-Chloroquinyl Methacrylate: Synthesis, Characterization and In Vitro 2-Hydroxychloroquine Delivery Application

The Poly(2-chloroquinyl methacrylate-co-2-hydroxyethyl methacrylate) (CQMA-co-HEMA) drug carrier system was prepared with different compositions through a free-radical copolymerization route involving 2-chloroquinyl methacrylate (CQMA) and 2-hydroxyethyl methacrylate) (HEMA) using azobisisobutyronitrile as the initiator. 2-Chloroquinyl methacrylate monomer (CQMA) was synthesized from 2-hydroxychloroquine (HCQ) and methacryloyl chloride by an esterification reaction using triethylenetetramine as the catalyst. The structure of the CQMA and CQMA-co-HEMA copolymers was confirmed by a CHN elementary analysis, Fourier transform infra-red (FTIR) and nuclear magnetic resonance (NMR) analysis. The absence of residual aggregates of HCQ or HCQMA particles in the copolymers prepared was confirmed by a differential scanning calorimeter (DSC) and XR-diffraction (XRD) analyses. The gingival epithelial cancer cell line (Ca9-22) toxicity examined by a lactate dehydrogenase (LDH) assay revealed that the grafting of HCQ onto PHEMA slightly affected (4.2–9.5%) the viability of the polymer carrier. The cell adhesion and growth on the CQMA-co-HEMA drug carrier specimens carried out by the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) (MTT) assay revealed the best performance with the specimen containing 3.96 wt% HCQ. The diffusion of HCQ through the polymer matrix obeyed the Fickian model. The solubility of HCQ in different media was improved, in which more than 5.22 times of the solubility of HCQ powder in water was obtained. According to Belzer, the in vitro HCQ dynamic release revealed the best performance with the drug carrier system containing 4.70 wt% CQMA.

Preparation, Characterization and Properties of some Acrylic Base Latex: A Review

Acrylic polymer latex has versatile role in many academic and industrial applications like paint, adhesives, textile, paper industry, concrete, surface coating, synthetic rubber and many ones. Acrylic base polymer latex can be prepared by various polymerization methods like Batch emulsion, Seeded emulsion, Situ miniemulsion, Atom transfer radical, Free radical copolymerization, Pickering miniemulsion, Semi-continuous seeded emulsion, dispersion copolymerization, aqueous suspension polymerization etc. in different solvents i.e. 1,1,2-trichloroethane, water, deionized water, 1,4-dioxane, chloroform, tetra hydro furan, toluene, benzene, nitric acid and so on. Acrylic latexes possessed various properties such as increased particle size which resist centrifugal nature and reduce viscosity of heavy oil, layered coating on steel improve lustre along with flexibility, tensile strength and thermal stability too. Acrylic latexes increase silicon intensity in silicon nanoparticles by controlling pH of emulsion during polymerization and also super paramagnetic behaviour of Fe2O3 nanocomposites latex controlled by pH. In this connection, many researchers have synthesized various acrylic base polymer latex or its composites, investigate its utility in different forms for different purposes to improve properties as required. In this review our main emphasis is to investigate the synthesis, characterisation and application of various acrylate polymer latexes.

BSA Adsorption and Antibiofilm Properties of (N-Cyclohexylacrylamide-co-Acrylamide/AMPSNa) Hydrogels

The hydrogels poly (N-cyclohexylacrylamide-co-acrylamide/2-acrylamido-2-methyl-1-propanesodiumsulfonate) i.e.poly(NCA-co-AM/AMPSNa) (HG41,HG42,HG43&HG44) were synthesised via free-radical copolymerization of NCA and (AM) in a fixed proportion (50:50), but varying the ionic monomer-AMPSNa (0.1g,0.3g,0.5 d 0.7g) in a medium of mixture of water and methanol at 60°C in an oil bath, Potassium persulfate (KPS) was used as an initiator, while N,N'-methylene-bisacrylamide (MBA) was used as a cross-linker. FT-IR spectral data, SEM, XRD, and TGA techniques were used to characterise the synthesised hydrogel (HG43). On changing pH(3.0, 5.0, 7.0 & 9.0), the amount of Bovine Serum Albumin (BSA) adsorption efficiency by these hydrogels was evaluated. At pH 5.0, which is near to BSA's isoelectric point (4.7)., the maximum adsorption was found. BSA adsorption increased as the amount of AMPSNa increased. SEM and XRD were used to examine the BSA-adsorbed hydrogel (HG43). The antibiofilm abilities of the hydrogel (HG43) by Microtiter plate Assay(MTP), Fluorescence microscopy and SEMl against Staphylococcus aureus and Pseudomonas aureginosa displayed outstanding efficacy.

Influence of Newly Organosolv Lignin-Based Interface Modifier on Mechanical and Thermal Properties, and Enzymatic Degradation of Polylactic Acid/Chitosan Biocomposites

This article aimed to study the effects of chitosan fiber and a newly modifying agent, based on organosolv lignin, on mechanical and thermal performances and the enzymatic degradation of PLA/chitosan biocomposites. A newly modifying agent based on polyacrylic acid-grafted organosolv lignin (PAA-g-OSL) was synthesized via free radical copolymerization using t-butyl peroxide as the initiator. The biocomposites were prepared using an internal mixer and the hot-pressed method at various fiber loadings. The results demonstrate that the addition of chitosan fiber into PLA biocomposites remarkably decreases tensile strength and elongation at break. However, it improves the Young’s modulus. The modified biocomposites clearly demonstrat an improvement in tensile strength by approximately 20%, with respect to the unmodified ones, upon the presence of PAA-g-OSL. Moreover, the thermal stability of the modified biocomposites was enhanced significantly, indicating the effectiveness of the thermal protective barrier of the lignin’s aromatic structure belonging to the modifying agent during pyrolysis. In addition, a slower biodegradation rate was exhibited by the modified biocomposites, relative to the unmodified ones, that confirms the positive effects of their improved interfacial interaction, resulting in a decreased area that was degraded through enzyme hydrolysis.

A Zwitterionic Copolymer as Rheology Modifier and Fluid Loss Agents for Water-Based Drilling Fluids

To overcome the negative impact on the rheological and filtration loss properties of drilling fluids caused by elevated temperature and salts contamination, which are common in ultradeep or geothermal drilling operations, it is imperative to develop highly efficient additives used in the water-based drilling fluid. In this study, a zwitterionic copolymer P (AM/DMC/AMPS/DMAM, ADAD) was synthesized by using acrylamide (AM), cationic monomer methacrylatoethyl trimethyl ammonium chloride (DMC), anionic monomer 2-acrylamide-2-methyl propane sulfonic acid (AMPS), and N,N-dimethylacrylamide (DMAM) through free radical copolymerization. The copolymer was characterized by 1H Nuclear Magnetic Resonance (NMR), Fourier transform infrared spectroscopy (FTIR), elemental analysis, thermogravimetric analysis (TGA), and zeta potential. The rheological behavior, filtration properties, and the performance exposure to salt or calcium contamination in water-based drilling fluid were investigated. The bentonite/polymer suspension showed improved rheological and filtration properties even after aging at 160 °C or a high concentration of salt and calcium. The filtration loss can be greatly reduced by more than 50% (from 18 mL to 7 mL) by the inclusion of 2.0 wt% copolymer, while a slight increase in the filtrate loss was observed even when exposed to electrolyte contamination. Particle size distribution and zeta potential further validate the idea that zwitterionic copolymer can greatly improve the stability of base fluid suspension through positive group enhanced anchoring on the clay surface and repulsion force between negative particles. Moreover, this study can be directed towards the design and application of zwitterionic copolymer in a water-based drilling fluid.