Stabilizing Na-bentonite by Poly(Diallyl Dimethyl Ammonium Chloride) Adsorption

Clay minerals have been modified by polymers for different applications. The polymer addition affects not only the surface propertiesbut also the rheological properties and the stability of the clay-polymer suspension as a whole. In the current study, the electro-chemical properties of bentonite particles in presence of poly diallyl dimethyl ammonium chloride (PDDACl) were investigated. Theseproperties were characterized by as zeta potential, adsorption isotherm, Fourier transform infrared (FTIR) and the apparent viscosityat different solid percent. The results indicated that the viscosity of the bentonite-PDDACl suspension not only increases by raising thepolymer concentration but also by increasing solids %. Adsorption of PDDACl polymer increases the positivity of bentonite surfaceas a function of polymer concentration, which could be explained mainly by electrostatic interaction of deficient metal ions at theoctahedral sheets of bentonite with the cationic head group of the polymer. The PDDACl adsorption isotherm on bentonite fits moreprobably Langmuir than Freundlich isotherm

Enhanced water oxidation of CoP/CNTs via interfacial charge transfer induced by poly dimethyl diallyl ammonium chloride

CoP layer was successfully deposited onto poly(diallyl dimethyl ammonium chloride) (PDDA) functionalized carbon nanotubes (CoP/PDDA@CNTs) as high effective OER electrocatalysts in alkaline solution.

Microbicidal Dispersions and Coatings from Hybrid Nanoparticles of Poly (Methyl Methacrylate), Poly (Diallyl Dimethyl Ammonium) Chloride, Lipids, and Surfactants

Hybrid and antimicrobial nanoparticles (NPs) of poly (methyl methacrylate) (PMMA) in the presence of poly (diallyl dimethyl ammonium) chloride (PDDA) were previously obtained by emulsion polymerization in absence of surfactant with low conversion. In the presence of amphiphiles such as cetyl trimethyl ammonium bromide (CTAB), dioctadecyl dimethyl ammonium bromide (DODAB) or soybean lecithin, we found that conversion increased substantially. In this work, the effect of the amphiphiles on the NPs core-shell structure and on the antimicrobial activity of the NPs was evaluated. NPs dispersions casted on silicon wafers, glass coverslips or polystyrene substrates were also used to obtain antimicrobial coatings. Methods for characterizing the dispersions and coatings were based on scanning electron microscopy, dynamic light scattering, determination of thickness, rugosity, and wettability for the coatings and determination of colony-forming unities (log CFU/mL) of microbia after 1 h interaction with the coatings or dispersions. The amphiphiles used during PMMA/PDDA/amphiphile NPs synthesis reduced the thickness of the NPs PDDA shell surrounding each particle. The antimicrobial activity of the dispersions and coatings were due to PDDA—the amphiphiles were either washed out by dialysis or remained in the PMMA polymeric core of the NPs. The most active NPs and coatings were those of PMMA/PDDA/CTAB—the corresponding coatings showed the highest rugosity and total surface area to interact with the microbes. The dispersions and coatings obtained by casting of the NPs dispersions onto silicon wafers were hydrophilic and exhibited microbicidal activity against Escherichia coli, Staphylococcus aureus, and Candida albicans. In addition, a major effect of reduction in particle size revealed the suitability of nanometric and cationic NPs (sizes below 100 nm) represented by PMMA/PDDA/CTAB NPs to yield maximal microbicidal activity from films and dispersions against all microbia tested. The reduction of cell viability by coatings and dispersions amounted to 6–8 logs from [PDDA] ≥ minimal microbicidal concentration.