Antibacterial potential of electrochemically exfoliated graphene sheets

Electrochemically exfoliated graphene is functionalized graphene with potential application in biomedicine. Two most relevant biological features of this material are its electrical conductivity and excellent water dispersibility. In this study we have tried to establish the correlation between graphene structure and its antibacterial properties. The exfoliation process was performed in a two electrode-highly oriented pyrolytic graphite electrochemical cell. Solution of ammonium persulfate was used as an electrolyte. Exfoliated graphene sheets were dispersed in aqueous media and characterized by atomic force microscopy, scanning electron microscopy, Raman spectroscopy, Fourier transform infrared spectroscopy, X photoelectron spectroscopy, X-ray diffraction, electron paramagnetic resonance, zeta potential, contact angle measurements and surface energy. Antibacterial assays have shown lack of the significant antibacterial activity. Major effect on bacteria was slight change of bacteria morphology. Membrane remained intact despite significant change of chemical content of membrane components.This is the peer reviewed version of the paper: Marković, Z. M., Matijašević, D. M., Pavlović, V. B., Jovanović, S. P., Holclajtner-Antunović, I. D., Špitalský, Z., Mičušik, M., Dramićanin, M. D., Milivojević, D. D., Nikšić, M. P., & Todorović Marković, B. M. (2017). Antibacterial potential of electrochemically exfoliated graphene sheets. Journal of Colloid and Interface Science, 500, 30–43. [https://doi.org/10.1016/j.jcis.2017.03.110][https://www.sciencedirect.com/science/article/abs/pii/S0021979717303776?via%3Dihub

Surface modification of low-density polyethylene with poly(2-ethyl-2- oxazoline) using a low-pressure plasma treatment

Low-density polyethylene (LDPE) is a suitable polymer for biomedical applications due to its good physiochemical properties, but its insufficient biocompatibility is often an issue. Therefore, biocompatible substances such as those based on 2-ethyl-2-oxazoline seem to be a good choice to increase the LDPE biocompatibility. In this work, the surface modification of LDPE with poly(2-ethyl-2-oxazoline) with two different end-groups was investigated. This modification led to the improvement of surface and adhesion properties, which were investigated by several analytical methods. The low-temperature plasma treatment of the LDPE surface was sufficient to create binding sites for the permanent attachment of poly(2ethyl-2-oxazoline) chains. This was confirmed by infrared spectroscopy and X-Ray photoelectron spectroscopy. It was found that the polymer containing the acrylic end-group was well attached to the LDPE surface. 2013 Elsevier Ltd. All rights reserved.This work was supported by the Slovak Grant Agency VEGA for projects Nr. 2/0064/10 , Nr. 2/0151/12 , and Nr. 2/0185/10 ). The Center for Materials, Layers and Systems for Applications and Chemical Processes under Extreme Conditions was supported by the Research & Development Operational Program funded by the ERDF. Electron microscopy at IMC was performed with financial support through grant TACR TE01020118 .Scopu

Size effects of graphene nanoplatelets on the properties of high-density polyethylene nanocomposites: Morphological, thermal, electrical, and mechanical characterization

High-density polyethylene (HDPE)-based nanocomposites incorporating three different types of graphene nanoplatelets (GnPs) were fabricated to investigate the size effects of GnPs in terms of both lateral size and thickness on the morphological, thermal, electrical, and mechanical properties. The results show that the inclusion of GnPs enhance the thermal, electrical, and mechanical properties of HDPE-based nanocomposites regardless of GnP size. Nevertheless, the most significant enhancement of the thermal and electrical conductivities and the lowest electrical percolation threshold were achieved with GnPs of a larger lateral size. This could have been attributed to the fact that the GnPs of larger lateral size exhibited a better dispersion in HDPE and formed conductive pathways easily observable in scanning electron microscope (SEM) images. Our results show that the lateral size of GnPs was a more regulating factor for the above-mentioned nanocomposite properties compared to their thickness. For a given lateral size, thinner GnPs showed significantly higher electrical conductivity and a lower percolation threshold than thicker ones. On the other hand, in terms of thermal conductivity, a remarkable amount of enhancement was observed only above a certain filler concentration. The results demonstrate that GnPs with smaller lateral size and larger thickness lead to lower enhancement of the samples' mechanical properties due to poorer dispersion compared to the others. In addition, the size of the GnPs had no considerable effect on the melting and crystallization properties of the HDPE/GnP nanocomposites. © 2020 Evgin et al.This work was partially supported by the Science Grant Agency VEGA, project no. 2/0010/18, and 2/0093/16 (Slovakia).2/0010/18, 2/0093/1

Thermal and electrical characterization of multi-walled carbon nanotubes reinforced polyamide 6 nanocomposites

In this study composites of polyamide 6 and multiwalled carbon nanotubes (MWCNT) were prepared by diluting a masterbatch using melt mixing. Differential scanning calorimetry was employed in order to investigate the influence of nanotubes on the thermal transitions of polyamide 6. Significant changes are reported on crystallization and glass transition by the addition of nanotubes. The results are discussed in terms of polymer-filler interactions. Dielectric relaxation spectroscopy measurements were performed to study both the electrical and dielectric properties of the nanocomposites. Percolation threshold is calculated to be at 1.7 vol.% MWCNT

Structure-property relationships in polyamide 6/multi-walled carbon nanotubes nanocomposites

Polyamide 6 (PA6)/multi-walled carbon nanotubes (MWCNT) nanocomposites were produced by diluting a masterbach containing 20 wt % nanotubes using melt mixing. The influence of the addition of well dispersed MWCNT (as indicated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM)) on the thermal transitions, and crystallization behavior of the PA6 matrix is investigated. Differential scanning calorimetry (DSC) results show a reduction in heat capacity jump at the glass transition which is interpreted by an immobilized interfacial layer near the nanotubes. Furthermore, both DSC and X-ray diffraction (XRD) measurements indicate that nanotubes favor the formation of the α crystalline form of PA6. These findings are correlated with the observed improvement of the storage modulus as revealed by dynamic mechanical thermal analysis (DMTA). Additionally, a new crystallization peak appears when MWCNT are added, and is attributed to the formation of a different morphology of the same type crystallite around the nanotubes walls (trans-crystallinity). Finally, water sorption measurements show an increase of water content, normalized to the amorphous polymer fraction, in the nanocomposites. © 2009 Wiley Periodicals, Inc