10 research outputs found
The Impact of Polymer Grafting from a Graphene Oxide Surface on Its Compatibility with a PDMS Matrix and the Light-Induced Actuation of the Composites
Poly(dimethyl siloxane) (PDMS)-based materials with improved photoactuation properties were prepared by the incorporation of polymer-grafted graphene oxide particles. The modification of the graphene oxide (GO) surface was achieved via a surface initiated atom transfer radical polymerization (SI ATRP) of methyl methacrylate and butyl methacrylate. The modification was confirmed by thermogravimetric analysis, infrared spectroscopy and electron microscopy. The GO surface reduction during the SI ATRP was investigated using Raman spectroscopy and conductivity measurements. Contact angle measurements, dielectric spectroscopy and dynamic mechanical analyses were used to investigate the compatibility of the GO filler with the PDMS matrix and the influence of the GO surface modification on its physical properties and the interactions with the matrix. Finally, the thermal conductivity and photoactuation properties of the PDMS matrix and composites were compared. The incorporation of GO with grafted polymer chains, especially poly(n-butyl methacrylate), into the PDMS matrix improved the compatibility of the GO filler with the matrix, increased the energy dissipation due to the improved flexibility of the PDMS chains, enhanced the damping behavior and increased the thermal conductivity. All the changes in the properties positively affected the photoactuation behavior of the PDMS composites containing polymer-grafted GO
Reversible Actuation Ability upon Light Stimulation of the Smart Systems with Controllably Grafted Graphene Oxide with Poly (Glycidyl Methacrylate) and PDMS Elastomer: Effect of Compatibility and Graphene Oxide Reduction on the Photo-Actuation Performance
This study is focused on the controllable reduction of the graphene oxide (GO) during the surface-initiated atom transfer radical polymerization technique of glycidyl methacrylate (GMA). The successful modification was confirmed using TGA-FTIR analysis and TEM microscopy observation of the polymer shell. The simultaneous reduction of the GO particles was confirmed indirectly via TGA and directly via Raman spectroscopy and electrical conductivity investigations. Enhanced compatibility of the GO-PGMA particles with a polydimethylsiloxane (PDMS) elastomeric matrix was proven using contact angle measurements. Prepared composites were further investigated through the dielectric spectroscopy to provide information about the polymer chain mobility through the activation energy. Dynamic mechanical properties investigation showed an excellent mechanical response on the dynamic stimulation at a broad temperature range. Thermal conductivity evaluation also confirmed the further photo-actuation capability properties at light stimulation of various intensities and proved that composite material consisting of GO-PGMA particles provide systems with a significantly enhanced capability in comparison with neat GO as well as neat PDMS matrix
Simplified synthesis of silver nanoparticles on graphene oxide and their applications in electrocatalysis
The Impact of Polymer Grafting from a Graphene Oxide Surface on Its Compatibility with a PDMS Matrix and the Light-Induced Actuation of the Composites
Nicotinamide-based supergelator self-assembling via asymmetric hydrogen bonding NH OC and H Br pattern for reusable, moldable and self-healable nontoxic fuel gels
Hypothesis
Development of highly efficient low-molecular weight gelators (LMWGs) for safe energy storage materials is of great demand. Energy storage materials as fuel gels are often achieved by construction of hybrid organic frameworks capable of multiple noncovalent interactions in self-assembly, which allow tuning required properties at the molecular level by altering individual building blocks of the LMWG. However, LMWGs have limited rechargeable capability due to their chemical instability.
Experiments
We designed, synthesized and characterized a novel, bio-inspired chiral gemini amphiphile derivative 1 containing N-hexadecyl aliphatic tails from quaternized nicotinamide-based segment and bromide anion showing supergelation ability in water, alcohols, aprotic polar and aromatic solvents, with critical gel concentrations as low as 0.1 and 0.035 wt% in isopropanol and water, respectively.
Findings
Nanostructural architecture of the network depended on the solvent used and showed variations in size and shape of 1D nanofibers. Supergelation is attributed to a unique asymmetric NH⋯OC, H⋯Br− hydrogen bonding pattern between H-2 hydrogens from nicotinamide-based segment, amide functional groups from chiral trans-cyclohexane-1,2-diamide-based segment and bromide ions, supporting the intermolecular amide–amide interactions appearing across one strand of the self-assembly. Gels formed from 1 exhibit high stiffness, self-healing, moldable and colorable properties. In addition, isopropanol gels of 1 are attractive as reusable, shape-persistent non-toxic fuels maintaining the chemical structure with gelation efficiency for at least five consecutive burning cycles.This publication was jointly supported by Qatar University and Chemical Institute, Slovak Academy of Sciences Grant IRCC-2020-004 . The findings achieved herein are solely the work of the authors. This work was supported by the Slovak Research and Development Agency (grant no. APVV-17-0324 ) as well as by the Grant Agency of the Ministry of Education of the Slovak Republic (VEGA projects no. 1/0712/18 and 1/0145/20). P.H. also acknowledges the support from the European Union?s Horizon 2020 research and innovation programme under grant no. 810701 . J.O. acknowledges the Ministry of Education, Youth and Sports of the Czech Republic?DKRVO (RP/CPS/2020/003). Authors thank to Dr. Emil ?vajdlenka, Faculty of Pharmacy, Comenius University in Bratislava for HRMS measurements and Center for Advanced Materials and Gas Processing Center at Qatar University for support with facilities. The publication of this article was funded by the Qatar National Library.Scopu
Simple, Reversible, and Fast Modulation in Superwettability, Gradient, and Adsorption by Counterion Exchange on Self-Assembled Monolayer
A simple fabrication method for preparation
of surfaces able to
switch from superhydrophobic to superhydrophilic state in a reversible
and fast way is described. A self-assembled monolayer (SAM) consisting
of quaternary ammonium group with aliphatic tail bearing terminal
thiol functionality was created on gold nano/microstructured and gold
planar surfaces, respectively. A rough nano/microstructured surface
was prepared by galvanic reaction on a silicon wafer. The reversible
counterion exchange on the rough surface resulted in a switchable
contact angle between <5° and 151°. The prewetted rough
surface with Cl<sup>–</sup> as a counterion possesses a superoleophobic
underwater character. The kinetics of counterion exchanges suggests
a long hydration process and strong electron ion pairing between quaternary
ammonium group and perfluorooctanoate counterion. Moreover, a wettability
gradient from superhydrophobic to superhydrophilic can be formed on
the modified rough gold surface in a robust and simple way by passive
incubation of the substrate in a counterion solution and controlled
by ionic strength. Furthermore, adsorption of gold nanoparticles to
modified plain gold surface can be controlled to a high extent by
counterions present on the SAM layer
The effect of short polystyrene brushes grafted from graphene oxide on the behavior of miscible PMMA/SAN blends
Synthesis, Antimycobacterial, Antifungal and Photosynthesis-Inhibiting Activity of Chlorinated N-phenylpyrazine-2-carboxamides †
A series of sixteen pyrazinamide analogues with the -CONH- linker connecting the pyrazine and benzene rings was synthesized by the condensation of chlorides of substituted pyrazinecarboxylic acids with ring-substituted (chlorine) anilines. The prepared compounds were characterized and evaluated for their antimycobacterial and antifungal activity, and for their ability to inhibit photosynthetic electron transport (PET). 6-Chloro-N-(4-chlorophenyl)pyrazine-2-carboxamide manifested the highest activity against Mycobacterium tuberculosis strain H37Rv (65% inhibition at 6.25 μg/mL). The highest antifungal effect against Trichophyton mentagrophytes, the most susceptible fungal strain tested, was found for 6-chloro-5-tert-butyl-N-(3,4-dichlorophenyl)pyrazine-2-carboxamide (MIC = 62.5 μmol/L). 6-Chloro-5-tert-butyl-N-(4-chlorophenyl)pyrazine-2-carboxamide showed the highest PET inhibition in spinach chloroplasts (Spinacia oleracea L.) chloroplasts (IC50 = 43.0 μmol/L). For all the compounds, the relationships between the lipophilicity and the chemical structure of the studied compounds as well as their structure-activity relationships are discussed