Copper coated multifunctional cotton fabrics

2017 ◽  
Vol 48 (2) ◽  
pp. 448-464 ◽  
Author(s):  
Azam Ali ◽  
Vijay Baheti ◽  
Jiri Militky ◽  
Zaman Khan ◽  
Veronika Tunakova ◽  
...  

The present work deals with the development of electrically conductive cotton fabrics by in-situ deposition of copper particles. The dynamic light scattering, scanning electron microscope, and X-ray diffraction techniques were employed to study the morphology of deposited copper particles. The utility of conductive fabrics was analyzed for electromagnetic shielding ability over frequency range of 30 MHz to 1.5 GHz. The electromagnetic interference shielding was found to increase with increase in number of dips, which was attributed to increased reflection of EM waves due to dense, uniform, and percolated network of conductive copper particles on the surface. The sample produced from 100 and 150 dips exhibited the maximum shielding ability of 10 dB and 13 dB, respectively. Furthermore, the role of deposited copper particles on antibacterial properties was examined against pathogenic bacteria such as Staphylococcus aureus and Escherichia coli. The S. aureus showed more sensitivity towards copper particles as zone of inhibitions increased from 9.5 to 15.5 mm. At the end, the durability of fabrics was examined against washing after application of binder. The fabrics showed good retention of the copper particles, proved by scanning electron microscopic microstructures and small loss in the conductivity of the material after washing.

2011 ◽  
Vol 6 (3) ◽  
pp. 155892501100600 ◽  
Author(s):  
Sunil Kumar Bajpai ◽  
Varsha Thomas ◽  
Manjula Bajpai

In this work, ZnO microparticles were in situ in the chitosan – attached cotton fabric following ‘equilibration – cum - hydrothermal’ approach to yield zinc oxide microparticles loaded cotton (ZOMLC) fabrics. The ZnO microparticles were characterized by surface plasmon resonance (SPR), X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. The ZOMLC fabric showed fair antibacterial action against model bacteria E.coli.


Materials ◽  
2019 ◽  
Vol 12 (19) ◽  
pp. 3249 ◽  
Author(s):  
Satoshi Idenoue ◽  
Yoshitaka Oga ◽  
Daichi Hashimoto ◽  
Kazuya Yamamoto ◽  
Jun-ichi Kadokawa

In this study, we have performed the preparation of reswellable amorphous porous celluloses through regeneration from hydrogels. The cellulose hydrogels were first prepared from solutions with an ionic liquid, 1-butyl-3-methylimidazolium chloride (BMIMCl), in different concentrations. Lyophilization of the hydrogels efficiently produced the regenerated celluloses. The powder X-ray diffraction and scanning electron microscopic measurements of the products suggest an amorphous structure and porous morphology, respectively. Furthermore, the pore sizes of the regenerated celluloses, or in turn, the network sizes of cellulose chains in the hydrogels, were dependent on the concentrations of the initially prepared solutions with BMIMCl, which also affected the tensile mechanical properties. It was suggested that the dissolution states of the cellulose chains in the solutions were different, in accordance with the concentrations, which representatively dominated the pore and network sizes of the above materials. When the porous celluloses were immersed in water, reswelling was observed to regenerate the hydrogels.


2020 ◽  
Vol 35 (4-5) ◽  
pp. 389-398
Author(s):  
Tarık Eren ◽  
Gülay Baysal ◽  
Faik Doğan

There is a growing interest in new type of biocidal compounds with antibacterial properties against bacteria. In this study, new antibacterial synthetic materials bearing curcumin and cationic polymers were synthesized. In the synthesis stage, the methacrylate functional cationic monomer was synthesized via the Michael addition route by using 3-acryloxy-2-hydroxypropyl methacrylate and 3-amino pyridine to obtain Monomer 1. Monomer 1 was further quaternized with hexyl bromide to obtain a cationic methacrylate functional monomer. Free-radical polymerization of Monomer 1 and methyl acrylate was conducted in the presence of azobisisobutyronitrile under dimethylformamide solvent. The composite formulation was conducted by using turmeric extract Curcuma longa (curcumin), hydroxyapatite, montmorillonite, and silver nitrate. The materials were analyzed by using the methods of X-ray diffraction, nuclear magnetic resonance, Fourier transform infrared spectroscopy, and scanning electron microscopy. The biocidal activities against the bacteria Escherichia coli, Listeria monocytogenes, Salmonella, and Staphylococcus aureus were analyzed using agar well diffusion method. From the Fourier transform infrared, X-ray diffraction, and scanning electron microscopy analysis results of the synthesized nanocomposites, it is seen that they form strong connections with the components added to the composites and form an exfoliated structure. According to the antibacterial analysis results, the nanocomposites obtained have showed a strong antibacterial resistance against E.coli, L.monocytogenes, Salmonella, and S. aureus bacteria, and the high inhibition zone areas were obtained.


2013 ◽  
Vol 78 (9) ◽  
pp. 1387-1395 ◽  
Author(s):  
Nebojsa Nikolic ◽  
Vesna Maksimovic ◽  
Goran Brankovic ◽  
Predrag Zivkovic ◽  
Miomir Pavlovic

Lead electrodeposition processes from the basic (nitrate) and complex (acetate) electrolytes were mutually compared by the scanning electron microscopic and the X-ray diffraction analysis of the produced powder particles. The shape of dendritic particles strongly depended on the type of electrolyte. The dendrites composed of stalk and weakly developed primary branches (the primary type) were predominantly formed from the basic electrolyte. The ramified dendrites composed of stalk and of both primary and secondary branches (the secondary type) were mainly formed from the complex electrolyte. In the both type of powder particles Pb crystallites were predominantly oriented in the (111) plane. Formation of powder particles of the different shape with the strong (111) preferred orientation was discussed and explained by the consideration of the general characteristics of the growth of a crystal in the electrocrystallization processes.


2014 ◽  
Vol 938 ◽  
pp. 210-214
Author(s):  
T.K. Jayasree ◽  
P. Predeep

High temperature superconducting (SC) 2212 BiSrCaCuO nanoparticles were prepared by Sol-Gel method. Precursor was characterized by X-ray diffraction (XRD) and scanning Electron micrography. The superconductor nanocomposites were fabricated by nanoparticles of the SC powder with NR/LLDPE blends. The superconductive properties of the sintered samples and the nanocomposites were studied. Transition to a superconducting state around 88K appeared in the parent sample and in the composites. The scanning electron microscopic investigation of the nanostructures of SC polymer ceramic nanocomposites shown nanoscale dispersion of BSCCO in the polymer phase uniformly.


2020 ◽  
Author(s):  
Ross Anderson ◽  
et al.

Supplemental methodological details, antibacterial properties of clays, other minerals with distinct fossil/matrix distributions, summaries of mineralogy by taxon, data tables, statistical summaries, and light/scanning electron microscopy–energy-dispersive X-ray spectroscopy images of fossil specimens showing X-ray diffraction selected areas.<br>


2021 ◽  
Vol 22 (3) ◽  
pp. 595-601
Author(s):  
R.G. Abaszade ◽  
S.A. Mamedova ◽  
F.G. Agayev ◽  
S.I. Budzulyak ◽  
O.A. Kapush ◽  
...  

We have synthesized large scale, thin, transparent graphene oxide (GO) flakes by Hummer’s method and investigated their suitability for fabrication of transparent nanocomposites. The GO flakes were comprehensively characterized by X-ray diffraction, Scanning Electron Microscopy (SEM), Energy Dispersive X-ray analysis (EDX), Raman spectroscopy and Differential Scanning Calorimetry (DSC). X-ray diffraction displayed the peak of graphene oxide at 9°degree, which is characteristic peak of GO in agreement with the literature results. Scanning Electron Microscopy images revealed that thin, transparent, flake form GO with 14,8 µm lateral size and 0,31µm thickness were synthesized. The comparison with literature results show that for the first time, our group could synthesize large scale, thin and more transparent GO flakes by simple Hummer’s method using simple dispersed graphite. EDX measurements indicate the formation of layered structure with oxygen containing functional groups. The intensity ratio between D and G peaks in the Raman spectra proves that less defective GO flakes have been synthesized. The solution ability of the synthesized material indicate that high quality GO flakes were synthesized, which make them effective soluble material due to oxygen containing groups formed on the graphene plane during synthesis process.DSC results shows that these flakes are thermally stable till 200°C.  Due to high solubility properties, large scale and transparency they can be very useful in fabrication of high optical transparent nanocompoties for replacement indium tin oxide transparent conductors in solar panels, biomedical applications and microwave absorbers for electromagnetic interference (EMI) environmental protection.


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