Morphology and mechanical properties of dual‐curable epoxyacrylate hybrid composites

A dual‐curable epoxyacrylate (EA) oligomer with one epoxide group and one vinyl group at each end was synthesized for the application as adhesive sealant in the liquid crystal display panels. However, after UV and thermal cure, the EA resin was brittle with a poor resistance to crack initiation and propagation. Liquid rubbers with different functional end groups were thus tried as toughening agents for the EA resin. Among all the rubber‐toughened EAs, the EA‐V5A5 added with vinyl‐terminated and amino‐terminated butadiene‐acrylonitrile copolymers (VTBN and ATBN) each at 5 phr had the highest fracture toughness, tensile strength, and elongation at break but a lower initial modulus. To raise the modulus, submicron‐sized silica particles (∼170 nm) with surface vinyl functional groups were further added to the EA‐V5A5 to prepare the hybrid composites. Because of interfacial chemical bonding provided by the surface vinyl functional groups, both modulus and fracture toughness were increased by adding silica particles, without any appreciable decrease in extensibility. For the hybrid composite at 20 phr silica particles, the initial modulus, fracture toughness, and fracture energy were raised by 10.3, 100, and 267%, respectively, when compared to the neat epoxyacrylate. Owing to their strong interfacial bonding, the increase of fracture toughness was mainly due to the crack deflection and bifurcation on silica particles, in addition to the rubber particle bridging and tearing as evidenced by SEM pictures on the fracture surface. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41820.     

Preparation of highly conductive reduced graphite oxide/poly(styrene-co-butyl acrylate) composites via miniemulsion polymerization

Polymer/reduced graphite oxide (rGO) composite nanoparticles with a high electrical conductivity were synthesized using the miniemulsion polymerization technique. The rGO was modified with a reactive surfactant, 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS), to facilitate monomer intercalation into the rGO nanogalleries. The AMPS-modified rGO was emulsified in the presence of styrene (St) and butyl acrylate (BA) monomers, and the stable miniemulsion was polymerized to form poly(St-co-BA)/rGO composite latex nanoparticles. The transition in the composite nanoparticles from an electrical insulator to an electrical conductor occurred at an rGO content of 10 wt% (relative to the monolayer content), yielding an electrical conductivity of 0.49 S/cm. The electrical conductivity of the composite nanoparticles reached 2.22 S/cm at 20 wt% rGO, yielding a much better conductivity than other polymer composites prepared using a GO filler. Importantly, the miniemulsion polymerization method for fabricating poly(St-co-BA)/rGO composite nanoparticles is easy, green, low-cost, and scalable, providing a universal route to the rational design and engineering of highly conductive polymer composites.     

Diameter and Density Control of Single‐Walled Carbon Nanotube Forests by Modulating Ostwald Ripening through Decoupling the Catalyst Formation and Growth Processes

A continuous and wide range control of the diameter (1.9?3.2 nm) and density (0.03?0.11 g cm^?3) of single‐walled carbon nanotube (SWNT) forests is demonstrated by decoupling the catalyst formation and SWNT growth processes. Specifically, by managing the catalyst formation temperature and H₂ exposure, the redistribution of the Fe catalyst thin film into nanoparticles is controlled while a fixed growth condition preserved the growth yield. The diameter and density are inversely correlated, where low/high density forests would consist of large/small diameter SWNTs, which is proposed as a general rule for the structural control of SWNT forests. The catalyst formation process is modeled by considering the competing processes, Ostwald ripening, and subsurface diffusion, where the dominant mechanism is found to be Ostwald ripening. Specifically, H₂ exposure increases catalyst surface energy and decreases diameter, while increased temperature leads to increased diffusion on the surface and an increase in diameter.     

Influence of High-Permeability Layers for Enhancing Landfill Gas Capture and Reducing Fugitive Methane Emissions from Landfills

Gas collection systems of various designs have been used to control landfill gas emissions, which can be problematic, particularly before installation of final landfill covers. In this work, an innovative gas collection system that includes a permeable layer near the top surface of landfills was evaluated for enhancing capture of landfill gas and reducing fugitive methane emissions. A computational model that accounts for advective and diffusive fluxes of multiple gas components was used to evaluate the efficiency of this new design for intermediate landfill covers. The utility of the high-permeability gas-conductive layer was illustrated for several conditions of interest including varying refuse permeability, varying degrees of permeability anisotropy, and temporal atmospheric pressure changes. Simulations showed that the permeable layer decreased methane emissions by 43% when the horizontal to vertical permeability ratio for refuse was kh/kv = 3 and the domain average kh = 3×10?12?m2, while reductions in methane emissions decreased to 17% for the same anisotropy but with kh = 10?11?m2. With this design, barometric pressure changes did not significantly affect oxygen intrusion or methane emission rates.     

Conversion of amorphous TiO2 coatings into their crystalline form using a novel microwave plasma treatment

Crystalline titanium dioxide (TiO₂) coatings have been widely used in photo-electrochemical solar cell applications. In this study, TiO₂ and carbon-doped TiO₂ coatings were deposited onto unheated titanium and silicon wafer substrates using a DC closed-field magnetron sputtering system. The resultant coatings had an amorphous structure and a post-deposition heat treatment is required to convert this amorphous structure into the photoactive crystalline phase(s) of TiO₂. This study investigates the use of a microwave plasma heat treatment as a means of achieving this crystalline conversion. The treatment involved placing the sputtered coatings into a 2.45 GHz microwave-induced nitrogen plasma where they were heated to approximately 550 °C. It was observed that for treatment times as short as 1 min, the 0.25-μm thick coatings were converted into the anatase crystalline phase of TiO₂. The coatings were further transformed into the rutile crystalline phase after treatments at higher temperatures. The doping of TiO₂ with carbon was found to result in a reduction in this phase transformation temperature, with higher level of doping (up to 5.8% in this study) leading to lower anatase-to-rutile transition temperature. The photoactivity performance of both doped and un-doped coatings heat-treated using both furnace and microwave plasma was compared. The carbon-doped TiO₂ exhibited a 29% increase in photocurrent density compared to that observed for the un-doped coating. Comparing carbon-doped coatings heat-treated using the furnace and microwave plasma, it was observed that the latter yielded a 19% increase in photocurrent density. This enhanced performance may be correlated to the differences in the coatings' surface morphology and band gap energy, both of which influence the coatings' photoabsorption efficiency.     

Fluorous Iminoalditols: A New Family of Glycosidase Inhibitors and Pharmacological Chaperones

A collection of new reversible glycosidase inhibitors of the iminoalditol type featuring N‐substituents containing perfluorinated regions has been prepared for evaluation of physicochemical, biochemical and diagnostic properties. The vast variety of feasible oligofluoro moieties allows for modular approaches to customised structures according to the intended applications, which are influenced by the fluorine content as well as the distance of the fluorous moiety from the ring nitrogen. The first examples, in particular in the D ‐galacto series, exhibited excellent inhibitory activities. A preliminary screen with two human cell lines showed that, at subinhibitory concentrations, they are powerful pharmacological chaperones enhancing the activities of the catalytically handicapped lysosomal D ‐galactosidase mutants associated with GM1 gangliosidosis and Morquio B disease.     

In-vivo human brain molecular imaging with a brain-dedicated PET/MRI system

Advances in the new-generation of ultra-high-resolution, brain-dedicated positron emission tomography-magnetic resonance imaging (PET/MRI) systems have begun to provide many interesting insights into the molecular dynamics of the brain. First, the finely delineated structural information from ultra-high-field MRI can help us to identify accurate landmark structures, thereby making it easier to locate PET activation sites that are anatomically well-correlated with metabolic or ligand-specific organs in the neural structures in the brain. This synergistic potential of PET/MRI imaging is discussed in terms of neuroscience and neurological research from both translational and basic research perspectives. Experimental results from the hippocampus, thalamus, and brainstem obtained with ¹⁸F-fluorodeoxyglucose and ¹¹C-3-amino-4-(2-dimethylaminomethylphenylsulfanyl)benzonitrile are used to demonstrate the potential of this new brain PET/MRI system.     

Isolation of Ambient Particles of Known Critical Supersaturation: The Differential Activation Separator (DAS)

A field-deployable instrument has been developed that isolates from an ambient aerosol those particles that have critical supersaturations, S_c, within a narrow, user-specified, range. This Differential Activation Separator (DAS) consists of two continuous flow diffusion chambers housed within a single enclosure. Particles are introduced into the upstream chamber referred to as the CCN remover (CCNR) near the centerline between a warm, water-soaked, plate and a cool, continuously circulated, water bath. Those particles that activate at the resulting peak supersaturation, S_p, grow quickly and fall into the water bath. The remaining aerosol enters the second chamber referred to as the CCN separator (CCNS), which differs from the CCNR primarily in the use of a salt solution in the lower bath. The imposed temperature differential establishes an S_p slightly higher than that maintained in the upstream chamber, while the presence of a salt solution at the lower boundary results in a subsaturated region in roughly the lower half of the chamber. Those particles having (S_p)_CCNR < S _c < (S_p)_CCNS activate in this chamber and begin to fall due to gravitational settling. Before reaching the lower bath, the droplets evaporate in the subsaturated environment and continue to travel towards the chamber exit. The previously activated particles in the lower half of the chamber and the unactivated particles in the upper half are extracted in separate flows that are subsequently dried. Calibration of the DAS was achieved by measuring the size distribution of separated particles when a polydisperse ammonium sulfate aerosol was introduced.