3D/4D printing of high-performance nanocomposites and AI/ML strategies

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Antimicrobial PVK:SWNT nanocomposite coated membrane for water purification: Performance and toxicity testing

This study demonstrated that coated nitrocellulose membranes with a nanocomposite containing 97% (wt%) of polyvinyl-N-carbazole (PVK) and 3% (wt%) of single-walled carbon nanotubes (SWNTs) (97:3 wt% ratio PVK:SWNT) achieve similar or improved removal of bacteria when compared with 100% SWNTs coated membranes. Membranes coated with the nanocomposite exhibited significant antimicrobial activity toward Gram-positive and Gram-negative bacteria (?80–90%); and presented a virus removal efficiency of ?2.5 logs. Bacterial cell membrane damage was considered a possible mechanism of cellular inactivation since higher efflux of intracellular material (Deoxyribonucleic acid, DNA) was quantified in the filtrate of PVK-SWNT and SWNT membranes than in the filtrate of control membranes. To evaluate possible application of these membrane filters for drinking water treatment, toxicity of PVK-SWNT was tested against fibroblast cells. The results demonstrated that PVK-SWNT was non toxic to fibroblast cells as opposed to pure SWNT (100%). These results suggest that it is possible to synthesize antimicrobial nitrocellulose membranes coated with SWNT based nanocomposites for drinking water treatment. Furthermore, membrane filters coated with the nanocomposite PVK-SWNT (97:3 wt% ratio PVK:SWNT) will produce more suitable coated membranes for drinking water than pure SWNTs coated membranes (100%), since the reduced load of SWNT in the nanocomposite will reduce the use of costly and toxic SWNT nanomaterial on the membranes

2,2'-(1,4-Phenylene)bis(propane-2,2-diyl) bis(benzodithioate)

The title compound, C26H26S4, shows a dihedral angle of 76.64 (15) between the central and peripheral benzene rings. An inversion center is located at the centroid of the thiobenzoyl ring. In the crystal, weak C-H...S interactions form C(5) chains along [001]. There are no classical hydrogen bonds.Universidad del ValleUniversidad de San Buenaventur

Tunable Protein and Bacterial Cell Adsorption on Colloidally Templated Superhydrophobic Polythiophene Films

A facile approach for enabling or inhibiting the adsorption of protein and adhesion of bacterial cells on a potential-induced reversibly wettable polythiophene film is described. The superhydrophobic polymeric surface was first prepared by a two-step process that combines the layering of polystyrene (PS) latex particles via a Langmuir–Blodgett (LB)-like technique followed by cyclic voltammetric (CV)–electrodeposition of polythiophene from a terthiophene ester monomer. The polythiophene conducting polymer coating enabled control of the wettability of the surface by simply changing its redox property via potential switching. The influence of morphology on this switching behavior is also described. The wettability in return controls the adsorption of protein and adhesion of bacterial cells. For instance, the undoped polythiophene film, which is superhydrophobic, inhibits the adhesion of fibrinogen proteins and Escherichia coli (E. coli) cells. On the other hand, the doped film, which is hydrophilic, leads to increased attachment of both protein and bacteria. Unlike most synthetic antiwetting surfaces, the as-prepared superhydrophobic coating is nonfluorinated. It maintains its superhydrophobic property at a wide range of pH (pH 1–13) and temperature (below ?10 °C and between 4 and 80 °C). Moreover, the surface demonstrated self-cleaning properties at a sliding angle as low as 3° ± 1. The proposed methodology and material should find application in the preparation of smart or tunable biomaterial surfaces that can be either resistant or susceptible to proteins and bacterial cell adhesion by a simple potential switching

3,5-Bis(benzyloxy)benzoic acid

In the title compound, 'C IND.21''H IND. 18''O IND. 4', the outer benzyl rings are disordered over two resolved positions in a 0.50 ratio. The O-C'H IND. 2' groups form dihedral angles of 4.1 (2) and 10.9 '(4) GRAUS' with the central benzene ring, adopting a syn-anti conformation with respect to this ring. In the crystal, the molecules are linked by O-H...O hydrogen bonds and weak C-H...O interactions, forming chains along [010]

Antimicrobial Applications of Electroactive PVK-SWNT Nanocomposites

The antibacterial properties of a nanocomposite containing an electroactive polymer, polyvinyl-N-carbazole (PVK) (97 wt %), and single-walled carbon nanotubes (SWNT) (3 wt %) was investigated as suspensions in water and as thin film coatings. The toxic effects of four different PVK-SWNT (97:3 wt %) nanocomposite concentrations (1, 0.5, 0.05, and 0.01 mg/mL) containing 0.03, 0.015, 0.0015, and 0.0003 mg/mL of SWNT, respectively, were determined for planktonic cells and biofilms of Escherichia coli (E. coli) and Bacillus subtilis (B. subtilis). The results showed that the nanocomposite PVK-SWNT had antibacterial activity on planktonic cells and biofilms at all concentration levels. Higher bacterial inactivation (94% for E. coli and 90% for B. subtilis) were achieved in planktonic cells at a PVK-SWNT concentration of 1 mg/mL. Atomic force microscopy (AFM) imaging showed significant reduction of biofilm growth on PVK-SWNT coated surfaces. This study established for the first time that the improved dispersion of SWNTs in aqueous solutions in the presence of PVK enhances the antimicrobial effects of SWNTs at very low concentrations. Furthermore, PVK-SWNT can be used as an effective thin film coating material to resist biofilm formation

Permeability of anti-fouling PEGylated surfaces probed by fluorescence correlation spectroscopy

The present work reports on in situ observations of the interaction of organic dye probe molecules and dye-labeled protein with different poly(ethylene glycol) (PEG) architectures (linear, dendron, and bottle brush). Fluorescence correlation spectroscopy (FCS) and single molecule event analysis were used to examine the nature and extent of probe朠EG interactions. The data support a sieve-like model in which size-exclusion principles determine the extent of probe朠EG interactions. Small probes are trapped by more dense PEG architectures and large probes interact more with less dense PEG surfaces. These results, and the tunable pore structure of the PEG dendrons employed in this work, suggest the viability of electrochemically-active materials for tunable surfaces