scholarly journals UV-light photocatalytic degradation of non-ionic surfactants using ZnO nanoparticles

Author(s):  
K. Huszla ◽  
M. Wysokowski ◽  
A. Zgoła-Grześkowiak ◽  
M. Staszak ◽  
M. Janczarek ◽  
...  

AbstractThe aim of this study was to evaluate the performance of zinc oxide nanoparticles as a photocatalyst for photodegradation of two model non-ionic surfactants (Triton X-100 and C12E10). The first part of the investigation was focused on the synthesis and characterization of ZnO nanoparticles, since its crystalline structure strongly impacts its photocatalytic properties. Based on the results of the XRD analysis, it was concluded that the obtained material occurred in the form of hexagonal wurtzite with a polycrystalline structure. FT-IR and XPS analyses were used to elucidate and confirm the nanomaterial structure, whereas investigation of N2 adsorption/desorption and SEM/TEM imaging allowed to establish that the synthesized ZnO was characterized as a mesoporous material with uniform, spherical shape and particle size fluctuating between 90 and 130 nm. The second part of the study included spectrophotometric assessment of the photodegradation process. The use of the obtained ZnO nanoparticles allowed to achieve efficient photodegradation of both C12E10 (92%) and Triton X-100 (82%) after 1 h of UV irradiation. The Langmuir–Hinshelwood mechanism was used to describe the reaction kinetics. Subsequent LC-MS/MS analysis of the residues indicated that the degradation mechanism is most likely based on both central fission of the surfactant molecules with further terminal oxidation of poly(ethylene glycol) and terminal oxidation leading to carboxylic derivatives of surfactants.

2013 ◽  
Vol 756 ◽  
pp. 167-174 ◽  
Author(s):  
Yim Leng Chan ◽  
Swee Yong Pung ◽  
Nur Syafiqah Hussain ◽  
Srimala Sreekantan ◽  
Fei Yee Yeoh

The oxide semiconductor with different band gap energy i.e. manganese dioxide (MnO2) (Eg: 1.30eV) and zinc oxide (ZnO) (Eg: 3.37 eV) nanoparticles were used to degrade RhodamineB (RhB) under irradiation of UV light (254 nm).The MnO2nanoparticles were synthesized by hydrothermal method (160 °C, 4 h) using analytical grade manganese sulfate hydrate and potassium permanganate (VII) as precursors. The XRD analysis reveals that the nanoparticles were d-MnO2.The photocatalytic study shows that degradation of RhB solution by ZnO nanoparticles (rate constant: 0.02749 min-1) was approximately four times faster than the d-MnO2nanoparticles (rate constant:0.0067 min-1). This observation could be attributed to the higher reducing and oxidizing power of ZnO in producing free radicals for photodegradation of RhB solution.


2008 ◽  
Vol 273-276 ◽  
pp. 198-203
Author(s):  
A. Esmaielzadeh Kandjani ◽  
Mohammad Reza Vaezi ◽  
Ali Shokuhfar ◽  
M. Farzalipour Tabriz

ZnO nanoparticles because of their interesting properties and various morphologies, has become one of the most attractive nanomaterials for research objectives. Its significant properties has made it applicable in UV-Light emitters, varistors, transparent high power electronics, gas sensors, etc., [1]. Many approaches have been used to obtain ZnO nanoparticles, including: Hydrothermal [2], Solvothermal [3], Reverse micelles [4], Sol-Gel [4], Sonochemical [5], and Chemical Bath Deposition [6], etc. Among these, hydrothermal and alcohol-thermal methods have been extremely investigated. In this paper, buthanol as a solvent is used for synthesis of Zinc oxide at 130°C and 150°C at different reaction periods. Also the effects of different surfactants including: N_Cetyl_N,N,N,_trimethyl ammonium bromide (CTAB), Poly vinyl pyrolidon-K90 (PVP), Poly ethylene glycol-15000 (PEG) on obtained morphologies were investigated extremely. X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM) were used for characterization of nanoparticles.


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.


2013 ◽  
Vol 678 ◽  
pp. 86-90
Author(s):  
P. Suresh Kumar ◽  
A. Dhayal Raj ◽  
R. Suresh ◽  
D. Mangalaraj

Intensive and innovative research is focused on the preparation of various nanostructured materials especially nanostructured metal oxides as applicable to number of applications.The present work mainly emphasis a single step synthesis of ZnO nanoparticles by employing surfactant free forced condensation method. Surface morphology of the sample was precisely controlled by varying the calcination conditions. Investigation on the structure, surface and composition of ZnO nanoparticles is of both fundamental interest and technological importance. X-ray diffraction (XRD) analysis reviled that the ZnO nanoparticles exhibits crystalline with the preferential orientation along (1 0 0) plane. SEM image shows the nanoparticles are in the range of 75 to 150 nm with spherical shape. The room temperature PL spectra of ZnO particles exhibited strong ultraviolet photoluminescence around 380 nm at room temperature.


Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 241
Author(s):  
Thangavel Ponrasu ◽  
Bei-Hsin Chen ◽  
Tzung-Han Chou ◽  
Jia-Jiuan Wu ◽  
Yu-Shen Cheng

The fast-dissolving drug delivery systems (FDDDSs) are developed as nanofibers using food-grade water-soluble hydrophilic biopolymers that can disintegrate fast in the oral cavity and deliver drugs. Jelly fig polysaccharide (JFP) and pullulan were blended to prepare fast-dissolving nanofiber by electrospinning. The continuous and uniform nanofibers were produced from the solution of 1% (w/w) JFP, 12% (w/w) pullulan, and 1 wt% Triton X-305. The SEM images confirmed that the prepared nanofibers exhibited uniform morphology with an average diameter of 144 ± 19 nm. The inclusion of JFP in pullulan was confirmed by TGA and FTIR studies. XRD analysis revealed that the increased crystallinity of JFP/pullulan nanofiber was observed due to the formation of intermolecular hydrogen bonds. The tensile strength and water vapor permeability of the JFP/pullulan nanofiber membrane were also enhanced considerably compared to pullulan nanofiber. The JFP/pullulan nanofibers loaded with hydrophobic model drugs like ampicillin and dexamethasone were rapidly dissolved in water within 60 s and release the encapsulants dispersive into the surrounding. The antibacterial activity, fast disintegration properties of the JFP/pullulan nanofiber were also confirmed by the zone of inhibition and UV spectrum studies. Hence, JFP/pullulan nanofibers could be a promising carrier to encapsulate hydrophobic drugs for fast-dissolving/disintegrating delivery applications.


Author(s):  
Anand Raj Lfa ◽  
Jeslin J

Objective: In this work, methanolic leaf extract from Cassia fistula (known as aragvadha) was incorporated into bentonite nanoclay to form organobentonite. This organobentonite of nanosize was further used for its effective biomedical applications since medicinal clay finds its own advantage over decades.Methods: The bentonite nanoclay was produced by energetic stirring followed by centrifugation and was characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared (FTIR). The organobentonite was produced using freeze and thaw method. Antioxidant property was studied using Molyneux method, and thrombolytic activity was analyzed using in vitro clot lysis method.Results: The nanosize of bentonite nanoclay between 57 and 82 nm with irregular to spherical shape was confirmed using SEM analysis. The sharp diffraction peak in XRD analysis shows the crystalline nature of bentonite nanoclay, and FTIR results revealed the successful incorporation of the methanolic extract within the bentonite nanoclay. The organobentonite exhibits 84.5% antioxidant property as well as 31% clot lysis activity when compared to the extract and the bentonite nanoclay.Conclusion: Thus, the non-toxic and inexpensive bentonite nanoclay have a high aspect ratio with multifarious applications in medicine, food, cosmetics, and health products. Through this study, the bentonite nanoclay modified using plant alkaloid (organobentonite) is found to possess good biomedical property.


Coatings ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1046
Author(s):  
M. Sharmila ◽  
R. Jothi Mani ◽  
Abdul Kader ◽  
Awais Ahmad ◽  
Gaber E. Eldesoky ◽  
...  

The innovation and development of water purification methods have been at the center of extensive research for several decades. Many nanoparticles are frequently seen in industrial waste water. In this research, zinc oxide nanoparticles (ZnO) were synthesized following an autocombustion method with and without honey capping. Structural crystallinity and bonding structure were examined via X-ray diffraction (XRD) analysis and Fourier transform infrared (FTIR) spectroscopy. Optical behavior was analyzed using ultraviolet–visible (UV–Vis) spectroscopy and photoluminescence (PL). Size estimation and surface morphology were studied using scanning electron microscopy (SEM), while energy-dispersive spectroscopy (EDS) was performed to analyze the sample purity and elemental composition. The photocatalytic degradation of methylene blue (MB) by ZnO was assessed as it is an efficient water treatment process with high potential. The biological activity of ZnO nanoparticles was also investigated in terms of antibacterial and antifungal activities against different bacterial and fungal species. Surprisingly, the as-synthesized ZnO nanoparticles were found to be substantially bioactive compared to conventional drugs. Honey-mediated nanoparticles displayed 86% dye degradation efficiency, and that of bare ZnO was 60%. Therefore, the involvement of honey in the synthesis of ZnO nanoparticles has great potential due to its dual applicability in both biological and environmental remediation processes.


2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Pardon Nyamukamba ◽  
Omobola Okoh ◽  
Lilian Tichagwa ◽  
Corinne Greyling

Herein, we describe the synthesis of titanium dioxide (TiO2) nanoparticles by the hydrolysis and condensation of titanium tetrachloride. The resulting nanoparticles were immobilized on polyacrylonitrile (PAN) based nanofibres by an electrospinning technique in order to allow simple isolation and reuse of titania semiconductor photocatalyst. The composite nanofibres were heat treated to convert the polymer nanofibres to carbon nanofibres and to convert amorphous TiO2to crystalline TiO2. X-ray diffraction (XRD) analysis showed that the rutile phase was the major phase and the equatorial peaks of PAN disappeared after heat treatment at 600°C. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) analysis confirmed that some TiO2nanoparticles were encapsulated whereas some were surface residing on the electrospun nanofibres. The TiO2nanoparticles were found to lower the cyclization temperature of PAN as indicated by differential scanning colorimetry (DSC) and differential thermal analysis (DTA). Photocatalytic studies on the degradation of methyl orange dye under UV light irradiation showed that composite nanofibres were capable of degrading organic contaminants in water. The carbon nanofibres with surface residing titanium dioxide nanoparticles (TiO2/CNF-SR) showed the highest photocatalytic activity (59.35% after 210 minutes) due to direct contact between the TiO2photocatalyst and methyl orange.


2014 ◽  
Vol 1081 ◽  
pp. 161-164
Author(s):  
Xue Mei Li ◽  
Zheng Guan ◽  
Hong Ling Liu ◽  
Jun Hua Wu ◽  
Xian Hong Wang ◽  
...  

FeAu/ZnO nanoparticles were successfully synthesized by nanoemulsion process with the use of poly (ethylene glycol)-block-poly (propylene glycol)-block-poly (ethylene glycol) as the surfactant. The characterization of the FeAu/ZnO nanoparticles was performed using X-ray powder diffraction (XRD), transmission electron microscopy (TEM) and UV-visible absorption spectroscopy, showing that the polymer-laced nanoparticles reveal high crystallinity, excellent dispersibility and well defined optical performance. The process of solvent dispersion-collection of FeAu/ZnO nanoparticles indicates that the nanoparticles possess good magnetic property for applications.


2013 ◽  
Vol 404 ◽  
pp. 20-24 ◽  
Author(s):  
Маzhyn Skakov ◽  
Bauyrzhan Rakhadilov ◽  
Gaukhar Karipbayeva

In this paper microstructure, morphology, elemental composition, phase composition and crystal structure of the sample steel R6M5 were investigate by using the methods of scanning electron microscopy, electron backscatter diffraction (EBSD) analysis and X-ray diffraction (XRD) analysis. Determined that the microstructure of steel R6M5 after hardening and three-time tempering consists of tempered martensite and solid carbide M6C and MC-type with spherical shape and a diameter of less than 3 μm. Detected that the volume fraction of each carbide amounted to 10.4±0.6% and 2.3±0.4% - for grey and bright carbides, respectively, and that the sizes of bright carbides particles in the microstructure of steel R6M5 are 0.4-4,5 μm, and the sizes of grey carbides particles are 0.5-1.1 μm. XRD analysis showed that the main carbides in the studied steel are carbides М6С and MC, which have complicated the FCC crystal lattice and the Fd3m spatial group. Determined that carbides are uniform and monocrystalline. ESBD analysis with the support of the XRD analysis showed that carbides spherical shape М6С fit to Fe3W3C composition.


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