One‐shot radical polymerization of vinyl monomers with different reactivity accompanying spontaneous delay of polymerization for the synthesis of double‐network hydrogels

Double‐network hydrogels were conveniently synthesized by the one‐shot radical polymerization of an ionic monomer for the first network and a non‐ionic monomer for the second network in the presence of crosslinkers by simultaneous addition of the monomers, that is, one‐shot and spontaneous two‐step polymerization accompanying the delay of polymerization of a second network monomer. We analyzed the polymerization process based on the conversion of each monomer during the reaction in the absence of crosslinkers. Then we fabricated the double‐network hydrogels using several polymerization systems consisting of a conjugated monomer and a non‐conjugated monomer in the presence of the dual crosslinkers. We analyzed the swelling, mechanical and viscoelastic properties of hydrogels synthesized by one‐shot radical polymerization to confirm the production mechanism and the network structure of the hydrogels. © 2020 Society of Chemical Industry     

Dip Coating of Water-Resistant PEDOT:PSS Films Based on Physical Crosslinking

Water-resistant poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films are valuable in biomedical applications; however, they typically require crosslinkers to stabilize the films, which can introduce undesired aggregation or phase separation reactions. Herein, a dipping-based process to prepare PEDOT:PSS films on nonplanar surfaces without crosslinker is developed. Sequential soaking of a dip-coated PEDOT:PSS film in ethanol and water imparts water resistance to the film. Microscopic and spectroscopic techniques are used to monitor the process and confirm that the ethanol soaking elutes the excess PSS from the film bulk, which stabilizes the film prior to the water-soaking process. The obtained films act as conductors and semiconductors on curved surfaces, including 3D-printed objects. A film deposited on a curved surface is successfully applied as the channel layer in a neuromorphic organic electrochemical transistor. This approach can enable integrated bioelectronic and neuromorphic applications that can be readily deployed for facile prototyping.     

Fabrication of TiO2 composite materials for air purification by magnetic field effect and electrocodeposition

Novel air purification materials were fabricated by the application of a magnetic field. In a magnetic field perpendicular to a copper plate, nickel particles with a diameter of 10 m were arranged to form numerous pillar-like structures on the matrix surface, and copper as a binder was deposited onto the three-dimensional surface. The total surface area of the pillars and the matrix increased with the magnetic flux density, up to about 800 cm² per cm² of the original matrix surface at 6.2 T. After successful codeposition of TiO₂ particles on the fabricated materials by electroplating, their photocatalytic activities were evaluated on the basis of the removal efficiency of nitrogen oxides (NO _x ), which are some of the most hazardous air pollutants. It was concluded that the samples with the pillar-like structures had two opposite characteristics: large surface area as a positive effect and shadowing against ultraviolet (UV) irradiation as a negative effect. However, total photocatalytic activity increased to twice as much as that of the flat sample by improving the UV irradiation method and the preparation condition of the materials     

Why would apparent κ linearly change with O/C? Assessing the role of volatility,solubility, and surface activity of organic aerosols

Correlations between O/C and cloud condensation nucleus activity, represented by κ, are a computationally efficient approach to estimate the impact of aerosol aging on cloud formation and climate; however, previously reported correlations between these two variables are empirical and vary widely in their slopes and extrapolations to high O/C values. This study proposes a theoretical framework that bridges elemental ratios, volatility, solubility, and κ. The framework estimates intrinsic κ based on molecular formulas of organics composed of carbon, oxygen, and hydrogen that partition to condensed phase, and then it estimates apparent κ considering solubility distribution parameterized by O/C. This article applied the new framework to the two-dimensional volatility basis set (2D-VBS) and found that distribution of O/C and molecular size play key roles in determining apparent κ. For highly soluble organics, κ is dictated by gas-particle partitioning and it is unlikely for κ of organics to go beyond 0.3 in typical ambient organic material loadings. Sensitivity analysis showed that surface-active compounds are not likely to profoundly alter the overall trend within a reasonable range of surface activity. This framework provides a simple yet plausible explanation of why κ would and would not correlate with O/C; distributions of OA in the 2D-VBS as well as the presence of inorganic salts determine the trend. The framework opens up new opportunities to evaluate two-dimensional representations of organic aerosol aging using κ, a significant advancement from the current empirical linear fits to κ and O/C.

Copyright © 2017 American Association for Aerosol Research     

A Unique Approach to Characterization of Sol‐Gel‐Derived Rare‐Earth‐Doped Oxyfluoride Glass‐Ceramics

Using the sol‐gel route Nd³⁺‐doped oxyfluoride glass‐ceramics were prepared. LiYF₄ and YF₃ crystals were deposited in the glass‐ceramics and their size, distribution, and amount ratio were varied by changing the compositions and heating temperatures. The incorporation of Nd³⁺ ions into both the fluoride crystals was confirmed by the high‐resolution elemental mapping of the glass‐ceramics. The incorporated Nd³⁺ ions showed up and down conversion photoluminescence whose properties were obviously different among the samples. The preliminary site analysis for Nd³⁺ ions was carried out using a unique approach associated with the Prony series approximation. Finally, the approach was found to be useful for the analysis of materials that are structurally complicating.     

Radiation detector made of a high-quality polycrystalline diamond

Radiation detector was made of a high-quality CVD polycrystalline diamond composed of frost column like structure diamond grains, and induced charge distribution spectra and drift velocities were measured by using alpha particles. As a result, the CVD polycrystalline achieved maximum induced charge of 83% of HP/HT type IIa diamond. Moreover, the CVD crystal had lower charge loss on electrons compared with the HP/HT type IIa diamond. Drift velocities of electrons and holes were v_e = 7.7 × 10⁴ and v_h = 7.3 × 10⁴cm/s at an electric field of 20 kV/cm, respectively. In addition, response function measurement for 14 MeV neutrons was carried out.     

Structural,electrical and electrochemical properties of polyacrylonitrile-ammonium hexaflurophosphate polymer electrolyte system

Polyacrylonitrile (PAN) based polymer electrolyte membranes complexed with Ammonium hexafluorophosphate (NH₄PF₆) with different molar concentration are prepared by solution casting method. Increase in the amorphous nature by the addition of Ammonium salt and the formation of polymer-salt complex are confirmed by X ray diffraction studies and infrared spectroscopy respectively. The glass transition temperature is measured for all membranes and it showed a lowest value for the PAN complexed with 20 mol% of NH₄PF₆. Electrical properties are studied by AC impedance spectroscopy. An ionic conductivity of the order of 10^?3 Scm^?1 is obtained for the 80 PAN / 20 NH₄PF₆ polymer electrolyte. Conductivity, dielectric and modulus spectra from the impedance data are analysed to understand the ionic transport mechanism. Transference number measurement is done to study the ionic contribution to the charge transport. A proton battery with the configuration, Zn+ ZnSO₄. 7H₂O /80 PAN / 20 NH₄PF₆ / PbO₂ +V₂O₅ has been constructed and its discharge characteristics are studied.     

1H NMR,thermal, and conductivity studies on PVAc based gel polymer electrolytes

The lithium‐ion conducting gel polymer electrolytes (GPE), PVAc‐DMF‐LiClO₄ of various compositions have been prepared by solution casting technique. ¹H NMR results reveal the existence of DMF in the gel polymer electrolytes at ambient temperature. Structure and surface morphology characterization have been studied by X‐ray diffraction analysis (XRD) and scanning electron microscopy (SEM) measurements. Thermal and conductivity behavior of polymer‐ and plasticizer‐salt complexes have been studied by differential scanning calorimetry (DSC), TG/DTA, and impedance spectroscopy results. XRD and SEM analyses indicate the amorphous nature of the gel polymer‐salt complex. DSC measurements show a decrease in T_g with the increase in DMF concentrations. The thermal stability of the PVAc : DMF : LiClO₄ gel polymer electrolytes has been found to be in the range of (30–60°C). The dc conductivity of gel polymer electrolytes, obtained from impedance spectra, has been found to vary between 7.6 × 10^?7 and 4.1 × 10^?4 S cm^?1 at 303 K depending on the concentration of DMF (10–20 wt %) in the polymer electrolytes. The temperature dependence of conductivity of the polymer electrolyte complexes appears to obey the VTF behavior. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008