Corrosion-protective coatings from electrically conducting polymers

In a joint effort between NASA Kennedy and LANL, electrically conductive polymer coatings were developed as corrosion protective coatings for metal surfaces. At NASA Kennedy, the launch environment consist of marine, severe solar, and intermittent high acid and/or elevated temperature conditions. Electrically conductive polymer coatings were developed which impart corrosion resistance to mild steel when exposed to saline and acidic environments. Such coatings also seem to promote corrosion resistance in areas of mild steel where scratches exist in the protective coating. Such coatings appear promising for many commercial applications

Substituted oligoanilines: synthesis and characterization

Abstract Substituted trimeric oligoanilines were synthesized by palladium-catalyzed aromatic amination, followed by hydrogenolysis or transamination and thermolysis. The effects of substituent groups on the electronic and electrochemical properties were characterized by cyclic voltammetry and UV-vis spectroscopy. Electron-donating groups decreased the oxidation potential and had little effect on the UV-vis absorption, while electron-withdrawing groups increased the oxidation potential and the UV-vis absorption wavelengths. Electrical conductivities were in the range from 10 −5 to 10 −3 S/cm when the oligoanilines were doped with iodine

Tobacco Mosaic Virus Based Thin Film Sensor for Detection of Volatile Organic Compounds

A thin film sensor for the detection of volatile organic compounds (VOC) was fabricated by deposition of oligo-aniline grafted tobacco mosaic virus (TMV) onto a glass substrate. The oligo-aniline motifs were conjugated onto the TMV surface by a traditional diazonium coupling reaction to tyrosine residues followed by Cu(I) catalyzed alkyne-azide cycloaddition (CuAAC) reaction. The modified TMV was easily fabricated into a thin film by directly drop coating onto a glass substrate. Upon integration of the glass substrate into a prototypical device, the virus-based thin film exhibited good sensitivity and selectivity toward ethanol and methanol vapour

Nanoparticles as Antibiotic-Delivery Vehicles (ADVs) Overcome Resistance by MRSA and Other MDR Bacterial Pathogens: The Grenade Hypothesis

Objectives The aim of this study was to examine how the concentrated delivery of less effective antibiotics, such as the Β-lactam penicillin G, by linkage to nanoparticles (NPs), could influence the killing efficiency against various pathogenic bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and other multidrug resistant (MDR) strains. Methods The Β-lactam antibiotic penicillin G (PenG) was passively sorbed to fluorescent polystyrene NPs (20 nm) that were surface-functionalized with carboxylic acid (COO−-NPs) or sulfate groups (SO4−-NPs) to form a PenG-NP complex. Antimicrobial activities of PenG-NPs were evaluated against Gram-negative and Gram-positive bacteria, including antibiotic resistant strains. Disc diffusion, microdilution assays and live/dead staining were performed for antibacterial assessments. Results The results showed that bactericidal activities of PenG-NP complexes were statistically significantly (P \u3c 0.05) enhanced against Gram-negative and Gram-positive strains, including MRSA and MDR strains. Fluorescence imaging verified that NPs comigrated with antibiotics throughout clear zones of MIC agar plate assays. The increased bactericidal abilities of NP-linked antibiotics are hypothesized to result from the greatly increased densities of antibiotic delivered by each NP to a given bacterial cell (compared with solution concentrations of antibiotic), which overwhelms the bacterial resistance mechanism(s). Conclusions As a whole, PenG-NP complexation demonstrated a remarkable activity against different pathogenic bacteria, including MRSA and MDR strains. We term this the ‘grenade hypothesis’. Further testing and development of this approach will provide validation of its potential usefulness for controlling antibiotic-resistant bacterial infections

The Mechanical Properties of Epoxy Composites Filled with Rubbery Copolymer Grafted SiO\u3csub\u3e2\u3c/sub\u3e

This study demonstrated a method for toughening a highly crosslinked anhydride cured DGEBA epoxy using rubbery block copolymer grafted SiO2 nanoparticles. The particles were synthesized by a sequential reversible addition-fragmentation chain transfer (RAFT) polymerization. The inner rubbery block poly(n-hexyl methacrylate) (PHMA) had a glass transition temperature below room temperature. The outer block poly(glycidyl methacrylate) (PGMA) was matrix compatible. A rubbery interlayer thickness of 100% and 200% of the particle core radius was achieved by grafting a 20 kg/mol and a 40 kg/mol PHMA at a graft density of 0.7 chains/nm2 from the SiO2 surface. The 20 kg/mol rubbery interlayer transferred load more efficiently to the SiO2 cores than the 40 kg/mol rubbery interlayer and maintained the epoxy modulus up to a loading of 10 vol% of the rubbery interlayer. Both systems enabled cavitation or plastic dilatation. Improvement of the strain-to-break and the tensile toughness was found in both systems. We hypothesize that plastic void growth in the matrix is the primary mechanism causing the improvement of the ductility

Engineering Nanoparticles to Silence Bacterial Communication

The alarming spread of bacterial resistance to traditional antibiotics has warranted the study of alternative antimicrobial agents. Quorum sensing (QS) is a chemical cell-to-cell communication mechanism utilized by bacteria to coordinate group behaviors and establish infections. QS is integral to bacterial survival, and therefore provides a unique target for antimicrobial therapy. In this study, silicon dioxide nanoparticles (Si-NP) were engineered to target the signaling molecules [i.e., acylhomoserine lactones (HSLs)] used for QS in order to halt bacterial communication. Specifically, when Si-NP were surface functionalized with β-cyclodextrin (β-CD), then added to cultures of bacteria (Vibrio fischeri), whose luminous output depends upon HSL-mediated QS, the cell-to-cell communication was dramatically reduced. Reductions in luminescence were further verified by quantitative polymerase chain reaction (qPCR) analyses of luminescence genes. Binding of HSLs to Si-NPs was examined using nuclear magnetic resonance (NMR) spectroscopy. The results indicated that by delivering high concentrations of engineered NPs with associated quenching compounds, the chemical signals were removed from the immediate bacterial environment. In actively-metabolizing cultures, this treatment blocked the ability of bacteria to communicate and regulate QS, effectively silencing and isolating the cells. Si-NPs provide a scaffold and critical stepping-stone for more pointed developments in antimicrobial therapy, especially with regard to QS—a target that will reduce resistance pressures imposed by traditional antibiotics

Effect of high magnetic fields on orientation and properties of liquid crystalline thermosets

In this report we provide the first description of the orientation of liquid crystalline thermosets (LCT`s) in field strengths of up to 18 T, as well as the first report of tensile properties for both unoriented and oriented LCT`S. The LCT we have chosen for study is the diglycidyl ether of dihydroxy-a-methylstilbene cured with the diamine, sulfanilamide. Orientation in magnetic fields leads to an increase of almost three times the modulus compared to the unoriented material. These values are much greater than can be obtained with conventional thermosets. The strain at break is also significantly affected by the chain orientation. The coefficient of thermal expansion and x-ray diffraction of oriented samples show high degrees of anisotropy, indicating significant chain alignment in the magnetic field. We are working to further understand the field dependence of orientation and properties plus the mechanisms of the alignment process

Engineering Nanoparticles to Silence Bacterial Communication

The alarming spread of bacterial resistance to traditional antibiotics has warranted the study of alternative antimicrobial agents. Quorum sensing (QS) is a chemical cell-to-cell communication mechanism utilized by bacteria to coordinate group behaviors and establish infections. QS is integral to bacterial survival, and therefore provides a unique target for antimicrobial therapy. In this study, silicon dioxide nanoparticles (Si-NP) were engineered to target the signaling molecules [i.e., acylhomoserine lactones (HSLs)] used for QS in order to halt bacterial communication. Specifically, when Si-NP were surface functionalized with β-cyclodextrin (β-CD), then added to cultures of bacteria (Vibrio fischeri), whose luminous output depends upon HSL-mediated QS, the cell-to-cell communication was dramatically reduced. Reductions in luminescence were further verified by quantitative polymerase chain reaction (qPCR) analyses of luminescence genes. Binding of HSLs to Si-NPs was examined using nuclear magnetic resonance (NMR) spectroscopy. The results indicated that by delivering high concentrations of engineered NPs with associated quenching compounds, the chemical signals were removed from the immediate bacterial environment. In actively-metabolizing cultures, this treatment blocked the ability of bacteria to communicate and regulate QS, effectively silencing and isolating the cells. Si-NPs provide a scaffold and critical stepping-stone for more pointed developments in antimicrobial therapy, especially with regard to QS—a target that will reduce resistance pressures imposed by traditional antibiotics

Synthesis of well-defined polymer brushes grafted onto silica nanoparticles via surface reversible addition-fragmentation chain transfer polymerization

ABSTRACT: Reversible addition-fragmentation chain transfer polymerization (RAFT) was used to prepare polymer brushes grafted onto silica nanoparticles. Novel RAFT-silane agents were prepared that contained both an active RAFT moiety and a silane coupling agent. RAFT agents were anchored to silica nanoparticles by the functionalization of colloidal silica with the RAFT-silane agents. RAFT polymerizations were then conducted from the particle surface to graft homopolymer and block copolymer brushes to the particles. The kinetics of styrene (St) and n-butyl acrylate (nBuA) surface RAFT polymerizations were investigated and compared with model polymerizations mediated by free RAFT agent. The molecular weights of grafted polymers increased linearly with conversions, and first-order kinetics were observed in the conversion range studied, indicating that the surface graft polymerization proceeded in a controlled manner. Well-defined PSt-block-PBuA copolymers attached to silica nanoparticles were also prepared