Fabrication and Characterization of Chitosan/Cellulose-ZnO Nanocomposites for Bactericidal Applications

2014 ◽  
Vol 1685 ◽  
Author(s):  
Melina Pérez-Altamar ◽  
Oscar Perales-Pérez

ABSTRACTThe present work focuses on the fabrication of environmental friendly ZnO nanocrystals and chitosan/cellulose films hosting ZnO nanoparticles (NPs) as an attempt to produce nanocomposites with enhanced bactericidal capacity. The solution casting method was used to fabricate the chitosan/cellulose blend films. Highly monodisperse ZnO nanoparticles were synthesized using Zinc acetate and Triethylene glycol (TEG) via a modified Polyol route. ZnO crystal size was controlled by the heterogeneous nucleation approach. Optical properties of ZnO nanoparticles were studied by UV–vis spectroscopy and Photoluminescence Spectroscopy (PL) techniques. The nanoparticles’ size and morphology were determined by Transmission Electron Microscopy (TEM) and X-ray diffraction (XRD), respectively. Obtained results confirmed the effectiveness of the size-controlled synthesis employed. The chitosan/cellulose/ZnO nanocomposites were characterized by Fourier Transform – Infrared spectroscopy (FTIR) and X-ray diffraction (XRD) methods. The mechanical properties of produced bare and ZnO-bearing composites were determined from stress-strain tests. The Standard Plate Count and the Halo Zone methods were used to evaluate the bactericidal properties of the ZnO nanoparticles, chitosan/cellulose blend films and chitosan/cellulose/ZnO nanocomposites againstEscherichia coli(ATCC 35218).

2015 ◽  
Vol 1804 ◽  
pp. 31-36 ◽  
Author(s):  
Melina Perez-Altamar ◽  
Hilary Marrero ◽  
Milton Martínez Julca ◽  
Oscar Perales Perez

ABSTRACTThe present work focuses on the polyol-mediated synthesis of pure and Mg-doped ZnO nanoparticles. The synthesized samples were characterized via X-ray diffraction, Fourier transformed infrared spectroscopy, ultraviolet visible spectroscopy and photoluminescence techniques. The Standard Plate Count was used to assess the bactericidal properties of the nanoparticles against E. coli at 1000 ppm and 1500 ppm of concentration. The capacity of the Zn-Mg oxides to generate singlet oxygen (SO) species was also evaluated. X-ray diffraction information evidenced the formation of ZnO-wurtzite; no diffraction peaks corresponding to isolated Mg-phases were detected. The average crystallite size of the Zn-Mg oxide nanocrystals was estimated in the 6nm - 7nm range. Infrared spectroscopy measurements confirmed the formation of the oxide with a Metal-Oxygen band centered on 536 cm-1; other bands associated to the functional groups of polyol by product were also observed. The exciton peak of UV spectrum suggests similarity in the particle size with the dopant addition. The effect of particle composition (i.e. doping level) on the corresponding generation of SO and bactericidal capacity is presented and discussed.


2017 ◽  
Vol 14 (2) ◽  
pp. 146-152
Author(s):  
Neha Sharma ◽  
Sanjayay Kumar

In present study, undoped ZnO, Zn0.8Ag0.2O, Zn0.8Al0.2O and Zn0.6Al0.2Ag0.2O samples are synthesized by simple solution method. X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), Energy-Dispersive X-ray spectroscopy (EDX) and UV-visible (UV-Vis) spectroscopy are used to perform the characterization of undoped, doped and codoped samples. XRD analysis is exposed that hexagonal wurtzite crystalline structure obtained for undoped, doped and codoped samples without any extra representation of impurity phases. The crystalline size is when evaluated by using Scherrer, It has 44, 49, 41and 37nm for undoped ZnO, Zn0.8Ag0.2O, Zn0.8Al0.2O and Zn0.6Al0.2Ag0.2O samples. Similarly, the crystalline size and strain are also evaluated by Williamson hall (W-H) and size strain plot (SSP) for the undoped, doped and codoped nanoparticles. The evaluated crystalline size by SSP is three times greater than the result of the scherrer method. The SEM exposes that surface morphology of nanoparticle samples, in this case is the formation of large agglomeration in spherical shape with nanocrystallites of undoped and doped ZnO with apparent and definite boundaries. EDX points out the replacement of Al2+ and Ag+ with Zn2+ in ZnO matrix and consequences in the development of single-phase Zn1−x−yAgxAlyO. The blueshift is shown in UV-Vis absorption spectra because the band gap value increases with the increase in doping, except Ag+ doped ZnO nanoparticles.


2019 ◽  
Vol 74 (10) ◽  
pp. 937-944 ◽  
Author(s):  
Babiker Y. Abdulkhair ◽  
Mutaz E. Salih ◽  
Nuha Y. Elamin ◽  
A. MA. Fatima ◽  
A. Modwi

AbstractStrenuous efforts have been employed to prepare zinc oxide (ZnO) with eco-friendly methods; however, few studies have reported the fabrication of ZnO using a sustainable procedure. In this study, spherical ZnO nanoparticles were successfully fabricated for photocatalysis applications using a simple and eco-friendly method using an arabinose sugar solution. The ZnO nanoparticles with a wurtzite structure were obtained by combining zinc nitrate and arabinose in water, followed by heating, evaporation, and calcinations at different annealing temperatures. The annealed ZnO photocatalysts were characterised via X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). The findings revealed a hexagonal wurtzite structure and good crystallinity with crystallite size increasing from 18 to 31 nm by means of an increase in the annealing temperature. The photocatalytic performance was examined to determine the degradation of mix dye waste. The spherical ZnO nanoparticles showed mix pollutant degradation of 84 % in 25 min at 400 °C.


1995 ◽  
Vol 382 ◽  
Author(s):  
Martin Pehnt ◽  
Douglas L. Schulz ◽  
Calvin J. Curtis ◽  
Helio R. Moutinho ◽  
Amy Swartzlander ◽  
...  

ABSTRACTIn this article we report the first nanoparticle-derived route to smooth, dense, phase-pure CdTe thin films. Capped CdTe nanoparticles were prepared by injection of a mixture of Cd(CH3)2, (n-C8H17)3 PTe and (n-C8H17)3P into (n-C8H17)3PO at elevated temperatures. The resultant nanoparticles 32-45 Å in diameter were characterized by x-ray diffraction, UV-Vis spectroscopy, transmission electron microscopy, thermogravimetric analysis and energy dispersive x-ray spectroscopy. CdTe thin film deposition was accomplished by dissolving CdTe nanoparticles in butanol and then spraying the solution onto SnO2-coated glass substrates at variable susceptor temperatures. Smooth and dense CdTe thin films were obtained using growth temperatures approximately 200 °C less than conventional spray pyrolysis approaches. CdTe films were characterized by x-ray diffraction, UV-Vis spectroscopy, atomic force microscopy, and Auger electron spectroscopy. An increase in crystallinity and average grain size as determined by x-ray diffraction was noted as growth temperature was increased from 240 to 300 °C. This temperature dependence of film grain size was further confirmed by atomic force microscopy with no remnant nanocrystalline morphological features detected. UV-Vis characterization of the CdTe thin films revealed a gradual decrease of the band gap (i.e., elimination of nanocrystalline CdTe phase) as the growth temperature was increased with bulk CdTe optical properties observed for films grown at 300 °C.


Author(s):  
Mateusz Gołdyn ◽  
Anna Komasa ◽  
Mateusz Pawlaczyk ◽  
Aneta Lewandowska ◽  
Elżbieta Bartoszak-Adamska

The study of various forms of pharmaceutical substances with specific physicochemical properties suitable for putting them on the market is one of the elements of research in the pharmaceutical industry. A large proportion of active pharmaceutical ingredients (APIs) occur in the salt form. The use of an acidic coformer with a given structure and a suitable pK a value towards purine alkaloids containing a basic imidazole N atom can lead to salt formation. In this work, 2,6-dihydroxybenzoic acid (26DHBA) was used for cocrystallization of theobromine (TBR) and caffeine (CAF). Two novel salts, namely, theobrominium 2,6-dihydroxybenzoate, C7H9N4O2 +·C7H5O4 − (I), and caffeinium 2,6-dihydroxybenzoate, C8H11N4O2 +·C7H5O4 − (II), were synthesized. Both salts were obtained independently by slow evaporation from solution, by neat grinding and also by microwave-assisted slurry cocrystallization. Powder X-ray diffraction measurements proved the formation of the new substances. Single-crystal X-ray diffraction studies confirmed proton transfer between the given alkaloid and 26DHBA, and the formation of N—H...O hydrogen bonds in both I and II. Unlike the caffeine cations in II, the theobromine cations in I are paired by noncovalent N—H...O=C interactions and a cyclic array is observed. As expected, the two hydroxy groups in the 26DHBA anion in both salts are involved in two intramolecular O—H...O hydrogen bonds. C—H...O and π–π interactions further stabilize the crystal structures of both compounds. Steady-state UV–Vis spectroscopy showed changes in the water solubility of xanthines after ionizable complex formation. The obtained salts I and II were also characterized by theoretical calculations, Fourier-transform IR spectroscopy (FT–IR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and elemental analysis.


2012 ◽  
Vol 31 (1) ◽  
pp. 79
Author(s):  
Khalil Faghihi ◽  
Masoumeh Soleimani ◽  
Shabnam Nezami ◽  
Meisam Shabanian

Two new samples of poly(amide-imide)-montmorillonite reinforced nanocomposites containing N-trimellitylimido-L-valine moiety in the main chain were synthesized by a convenient solution intercalation technique. Poly(amide-imide) (PAI) 5 as a source of polymer matrix was synthesized by the direct polycondensation reaction of N-trimellitylimido-L-valine (3) with 4,4′-diaminodiphenyl ether 4 in the presence of triphenyl phosphite (TPP), CaCl2, pyridine and N-methyl-2-pyrrolidone (NMP). Morphology and structure of the resulting PA-nanocomposite films (5a) and (5b) with 10 and 20 % silicate particles were characterized by FTIR spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM). The effect of clay dispersion and the interaction between clay and polymeric chains on the properties of nanocomposite films were investigated by using Uv-vis spectroscopy,  thermogravimetric analysis (TGA) and water uptake measurements.


2020 ◽  
Author(s):  
Viktoria Leonhardt ◽  
Stefanie Fimmel ◽  
Ana-Maria Krause ◽  
Florian Beuerle

<div><div><div><p>A trigonal-bipyramidal covalent organic cage compound serves as an efficient host to form stable 1:1-complexes with C60 and C70. Fullerene encapsulation has been comprehensively studied by NMR and UV/Vis spectroscopy, mass spectrometry as well as single-crystal X-ray diffraction. Exohedral functionalization of encapsulated C60 via threefold Prato reaction revealed high selectivity for the symmetry-matched all-trans-3 addition pattern.</p></div></div></div>


BioResources ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. 1548-1560
Author(s):  
Daniel Garcia-Bedoya ◽  
Luis P. Ramírez-Rodríguez ◽  
Jesús M. Quiroz-Castillo ◽  
Edgard Esquer-Miranda ◽  
Arnulfo Castellanos-Moreno

Algae constitute a diverse group that is useful in many biotechnological areas. In this paper, the usefulness of Caulerpa sertularioides methanol extract in the synthesis of ZnO and Zn(OH)2 nanoparticles was explored. This work had two main objectives: (1) to use the extract in the synthesis as an organic harmless complexing agent, and (2) to enhance a photocatalytic effect over AZO dyes in wastewater from fabric industries without adding nanomaterial to the environment due to its toxicity. Caulerpa extract performed the expected complexing action, and nanoparticles were formed in a size range from 45 to 69 nm. X-ray diffraction analysis (XRD), transmission electron microscopy (TEM) and UV-Vis spectroscopy were used to characterize the system. It was demonstrated that the nanoparticles were useful to photocatalyst AZO dyes in the water, while contained in tetraethylorthosilicate composites. These could be used in industrial wastewater and are expected to have no environmental consequences because the composites do not add nanoparticles to the water.


2014 ◽  
Vol 2 (4) ◽  
pp. 510-515
Author(s):  
Hala Moustafa Ahmed

The present study mainly focuses of combined action of Nepali hog plum as well as citrate synthesized silver nanoparticles (AgNPs) and Amikacin, as an antibiotic. The synergistic actions of citrate stabilized silver nanoparticles (AgNPs with chem) were compared with that of Nepali hog plum Choerospondia saxillaris (Lapsi) synthesized silver nanoparticles (AgNPs with plant), together with action of antibiotic onselected bacterial strains of Salmonella typhi. The synthesized AgNPs were characterized through UV-Vis spectroscopy, Transmission electronmicroscopy and X-ray diffraction technique. The size of the synthesized silver nanoparticles was measured by Transmission Electron Microscope (TEM) and X-ray diffraction (XRD).DOI: http://dx.doi.org/10.3126/ijasbt.v2i4.11127 Int J Appl Sci Biotechnol, Vol. 2(4): 510-515 


2021 ◽  
Vol 68 (1) ◽  
pp. 102-108
Author(s):  
Yu-Mei Hao

A mononuclear copper(II) complex, [CuL] (1), and a phenolato-bridged trinuclear zinc(II) complex, [Zn3Cl2L2(DMF)2] (2), where L is the deprotonated form of N,N’-bis(4-bromosalicylidene)propane-1,3-diamine (H2L), have been prepared and characterized by elemental analyses, IR and UV-Vis spectroscopy, and single crystal X-ray diffraction. The Cu atom in complex 1 is in square planar coordination, while the terminal and central Zn atoms in complex 2 are in square pyramidal and octahedral coordination, respectively. The antibacterial activities of the complexes have been tested on the bacteria Staphylococcus aureus and Escherichia coli, and the yeast Candida parapsilosis.


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