scholarly journals The Dependence of Photocatalytic Activity on Tio2 to MWCNT Ratio in the Composite

Author(s):  
Sedigheh Abbasi

Abstract Here, we prepared two kinds of nanocomposites (MCT#1 and MCT#2) involving MWCNTs and TiO2 nanopaerticles. The characterization of the samples is carried out based on FTIR spectroscopy and TEM. The Ti-O groups that is attibuted to the TiO2 nanopaerticles can be confirmed according to the FTIR analysis. TEM images show that the average particle size of TiO2 nanopaerticles in prepare MCT#1 and MCT#2 is equal to 13 nm and 15 nm, respectively. The influence of nanocomposites weight fraction and illumination time are investigated on the decomposition rate of methyl orange (MO) as pollutant. The photocatalytic results exhibit that the decomposition rate of MO is increased with respect to the weight fraction and illumination time. Meanwhile, higher decomposition rate can be observed using MCT#2 compared to MCT#1. Statistical analysis of the results based on Duncan’s multiple range test at α = 0.05 reveals that all of the applied levels of the factors have a significant effect on the decomposition rate. The response surface results confirm that the effect of illumination time is high that that of weight fraction of MCT#1 and MCT#2.

2011 ◽  
Vol 415-417 ◽  
pp. 617-620 ◽  
Author(s):  
Yan Su ◽  
Ying Yun Lin ◽  
Yu Li Fu ◽  
Fan Qian ◽  
Xiu Pei Yang ◽  
...  

Water-soluble gold nanoparticles (AuNPs) were prepared using 2-mercapto-4-methyl-5- thiazoleacetic acid (MMTA) as a stabilizing agent and sodium borohydride (NaBH4) as a reducing agent. The AuNPs product was analyzed by transmission electron microscopy (TEM), UV-vis absorption spectroscopy and Fourier transform infrared spectroscopy (FTIR). The TEM image shows that the particles were well-dispersed and their average particle size is about 5 nm. The UV-vis absorption and FTIR spectra confirm that the MMTA-AuNPs was stabilized by the carboxylate ions present on the surface of the AuNPs.


Author(s):  
Mohammed Sabar Al-lami ◽  
Malath H. Oudah ◽  
Firas A. Rahi

This study was carried out to prepare and characterize domperidone nanoparticles to enhance solubility and the release rate. Domperidone is practically insoluble in water and has low and an erratic bioavailability range from 13%-17%. The domperidone nanoparticles were prepared by solvent/antisolvent precipitation method at different polymer:drug ratios of 1:1 and 2:1 using different polymers and grades of poly vinyl pyrolidone, hydroxy propyl methyl cellulose and sodium carboxymethyl cellulose as stabilizers. The effect of polymer type, ratio of polymer:drug, solvent:antisolvent ratio, stirring rate and stirring time on the particle size, were investigated and found to have a significant (p? 0.05) effect on particle size. The best formula was obtained with lowest average particle size of 84.05. This formula was studied for compatibility by FTIR and DSC, surface morphology by FESEM and crystalline state by XRPD. Then domperidone nanoparticles were formulated into a simple capsule dosage form in order to study of the in vitro release of drug from nanoparticles in comparison raw drug and mixture of polymer:drug ratios of 2:1. The release of domperidone from best formula was highly improved with a significant (p? 0.05) increase.


2017 ◽  
Vol 263 ◽  
pp. 165-169
Author(s):  
Silvia Chowdhury ◽  
Faridah Yusof ◽  
Nadzril Sulaiman ◽  
Mohammad Omer Faruck

In this article, we have studied the process of silver nanoparticles (AgNPs) aggregation and to stop aggregation 0.3% Polyvinylpyrrolidone (PVP) was used. Aggregation study carried out via UV-vis spectroscopy and it is reported that the absorption spectrum of spherical silver nanoparticles were found a maximum peak at 420 nm wavelength. Furthermore, Transmission Electron Microscopy (TEM) were used to characterized the size and shape of AgNPs, where the average particle size is around 10 to 25 nm in diameter and the AgNPs shape is spherical. Next, Dynamic Light Scattering (DLS) were used, owing to observed size distribution and self-correlation of AgNPs.


2016 ◽  
Vol 18 (2) ◽  
pp. 131-139
Author(s):  
Kinga Łuczka ◽  
Barbara Grzmil ◽  
Bogumił Kic ◽  
Krzysztof Kowalczyk

Abstract Synthesis and characterization of the aluminum phosphates modified with ammonium, calcium and molybdenum were conducted. The influence of process parameters (reactive pressure and molar ratios) in the reaction mixture were studied. The contents of the individual components in the products were in the range of: 10.97–17.31 wt% Al, 2.65–13.32 wt% Ca, 0.70–3.11 wt% Mo, 4.36–8.38 wt% NH3, and 35.12–50.54 wt% P2O5. The materials obtained in the experiments were characterized by various physicochemical parameters. The absorption oil number was in the range from 67 to 89 of oil/100 g of product, the surface area was within the range of 4–76 m2/g, whereas the average particle size of products reached 282–370 nm. The Tafel tests revealed comparable anticorrosive properties of aluminum phosphates modified with ammonium, calcium, molybdenum in comparison with commercial phosphate.


2014 ◽  
Vol 793 ◽  
pp. 151-158 ◽  
Author(s):  
M. León-Carriedo ◽  
C.A. Gutiérrez Chavarría ◽  
J.L. Rodríguez Galicia ◽  
Jorge López-Cuevas ◽  
M.I. Pech Canul

In the present work, the characterization of monolithic materials formulated at different weight concentrations was conducted; employing two of the ceramic materials most used in the refractory industry, zircon and alumina. These monolithic materials were fabricated using colloidal techniques, specifically plaster casting mold, in order to obtain pieces with a higher particle consolidation and density, reducing porosity to lower values than the obtained using traditional shaping process of these materials. The monoliths were obtained employing two ceramic powders with different average particle size and morphology to achieve better packing in the green body. This characterization was carried out, firstly, determining the particle size of the raw materials by laser diffraction and the evaluation of particle morphology by scanning electron microscopy. Aqueous suspensions were formulated by containing both ceramic materials, which were dispersed with Tamol 963, and analyzed by rheometric techniques. Subsequently, bars were manufactured having the following dimensions; 4 mm wide, 3 mm thick and 45 mm in length, according to ASTM C1161-02cc, to be characterized microstructural and mechanically, also was observed the fracture habit after the mechanical test. As a final result, the materials formulated at higher alumina content showed higher density values, reaching 94.95% of the theoretical density, also showed a higher thermal expansion coefficient and high rupture modulus, reaching up to 600 MPa and Young modulus of 230 GPa. From the microstructure characterization it was observed that alumina matrix shows a transgranular fracture across the grains and zircon particles exhibited intergranular fracture among the grain boundaries.


Drug Research ◽  
2017 ◽  
Vol 67 (05) ◽  
pp. 266-270 ◽  
Author(s):  
Ebrahim Izadi ◽  
Ali Rasooli ◽  
Abolfazl Akbarzadeh ◽  
Soodabeh Davaran

AbstractThrough the present study, an eco-friendly method was used to synthesize the gold nanoparticles (GNPs) by using the sodium citrate and extract of the soybean seed as reducing the agents at PH 3. X-Ray diffraction (XRD) method was used to evaluate the crystal structure of as-synthesized NPs and it’s revealed that this method leads to well crystallized GNPs. In order to determine the particle size and their distribution, field emission scanning microscopy (FE-SEM) and dynamic light scattering (DLS) were used. The results showed that, the average particle size distribution of synthesized GNPs in solutions containing of the soybean extract and 1% citrate at PH 3 is about 109.6 and 140.9 nm, respectively. Also, we find that the average size of GNPs is 40 and 33 nm from solutions of citrate and soybean extract, respectively. It was concluded that using the extract of soybean seeds as reducing agent can lead to GNPs with small size and narrow size distribution.


2020 ◽  
Vol 20 (6) ◽  
pp. 3770-3779 ◽  
Author(s):  
Umar Farooq ◽  
Farheen Naz ◽  
Ruby Phul ◽  
Nayeem Ahmad Pandit ◽  
Sapan Kumar Jain ◽  
...  

This paper reports the attempt to develop an efficient heterostructure photocatalyst by employing SrZrO3 as ferroelectric substrate with deposited nanostructured CdS semiconductor on the surface. Primarily bare SrZrO3 and CdS nanoparticles were synthesized by using polymeric citrate precursor and co-precipitation routes, respectively. The chemical deposition technique was used to develop the CdS over the surface of the pre-synthesized SrZrO3 nanoparticles. The synthesized bare nanoparticles and their heterostructure were characterized by XRD which shows the formation of orthorhombic and face centred cubic (FCC) phases of SrZrO3 and CdS, respectively. TEM was used to estimate the morphology and particle size of as-synthesized nanoparticles, which shows the average particle size of 14, 24 and 25 nm for SrZrO3, CdS and SrZrO3/CdS, respectively. The BET surface area of SrZrO3, CdS and SrZrO3/CdS samples was found to be 299, 304 and 312 m2/g respectively. Methylene blue was used as model pollutant to determine the photocatalytic activity of the synthesized nanomaterials. The heterostructure shows an enhanced activity as compared to bare nanoparticles. Dielectric constant and dielectric loss of the nanoparticles was investigated as a function of frequency at room temperature and as a function of temperature at 500 kHz. The room temperature dielectric constant for SrZrO3, CdS and SrZrO3/CdS was found to be 13.2, 17.8 and 25.5 respectively at 100 kHz.


2020 ◽  
Vol 18 ◽  
Author(s):  
Yanfang Zhang ◽  
Rina Du ◽  
Pengwei Zhao ◽  
Sha Lu ◽  
Rina Wu ◽  
...  

Background: Quercetin is the main active ingredient of Xanthoceras sorbifolia Bunge. Traditional compatibility theory of traditional Chinese medicine has typically reported a synergistic interaction among multiple components, while the synergistic effects of nanoemulsion have not been fully clarified. Objective: To study preparation and characterization of quercetin-based Mongolia Medicine Sendeng-4 nanoemulsion (NQUE-NE) and its antibacterial activity and mechanisms. Methods: The morphology of the nanoemulsion was observed by transmission electron microscopy (TEM), and the zeta potential, polydispersity index (PDI), and particle size distribution were determined by the nanometer particle size analyze. The stability of nanoemulsion was investigated by light test, high speed centrifugal test and storage experiment at different temperature. The combined bacteriostatic effect of N-QUE-NE was studied in vitro by double-dilution method and checkerboard dilution method. Results: The appearance of N-QUE-NE was pale yellow, clear and transparent. The nanoemulsion particles were spherical and uniformly distributed under TEM. The PDI was 0.052, the average particle size was 19.6nm, and the Zeta potential was -0.2mV. When quercetin nanoemulsion (QUE-NE) was used in combination with tannin nanoemulsion (TAN-NE) and toosendanin nanoemulsion (TOO-NE), it exhibited a synergistic antibacterial effect. However, the combination of QUE-NE and geniposide nanoemulsion (GEN-NE) exhibited an antagonistic effect. It was revealed that the antibacterial effect was in order of quercetin-tannin-toosendanin nanoemulsion (QUE-TAN-TOO-NE) > quercetin-tannin nanoemulsion (QUE-TANNE) > QUE-NE > quercetin-tannin-toosendanin-geniposide nanoemulsion (QUE-TAN-TOO-GEN-NE). Conclusion: This study explored the preparation and efficacy of N-QUE-NE, and the results showed that quercetin, tannin and toosendanin had satisfactory synergistic antibacterial effects. The antagonistic effect of quercetin and geniposide in nanoemulsion indicated that it is not beneficial to the antibacterial effect of Sendeng-4, and further research needs to be conducted to clarify its antibacterial effect.


2016 ◽  
Vol 680 ◽  
pp. 198-202
Author(s):  
Chao Wang ◽  
Si Qin Zhao ◽  
S. Asuha

In this paper, a series of mesoporous TiO2 photocatalyst were prepared by hydrothermal method using block copolymer P123 as template and Ti (OBu)4 as titanium source. The microstructure and spectroscopy performance of the prepared TiO2 were characterized by means of XRD, SEM, TEM, BET, and BJH analysis, and the photocatalytic activity of mesoporous TiO2 were examined by measuring the photodegradation of methyl orange , then discussed the best prepared conditions of mesoporous TiO2 photocatalyst. The results showed that the products were all anatase mesoporous TiO2 nanopowder, the average particle size is about 7nm and all have the Langmuir type IV pore structure. The best prepared condition: hydrothermal temperature is 160°C, hydrothermal time is 24h, mesoporous TiO2 photocatalyst has the BET surface area of 146m2/g , it’s photocatalytic degradation rate is 97.07% in an hour.


2002 ◽  
Vol 01 (05n06) ◽  
pp. 539-543
Author(s):  
KYUNG WON SEO ◽  
SUNG DU MOON ◽  
YOUNG SOO KANG ◽  
YONG JOO KIM

Nanosize SiO 2 particles with narrow size distribution were produced by modified Stober–Fink–Bohn method. Average particle size was determined as 170 nm by SEM image. Organosilica mesoporous molecular sieve (MCM-48) was synthesized. The calcined MCM-48 has pore diameter of 26.8 Å and a surface area of 1024 m 2 g -1 by BET (Brunauer–Emmet–Teller) measurement.


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