Silver Nanoparticles in TiO2 Coatings for Potential Antimicrobial Coatings

2015 ◽  
Vol 1087 ◽  
pp. 20-24
Author(s):  
M.R. Zulkifli ◽  
A.R. Nurhamizah ◽  
Jariah Mohd Juoi ◽  
Zaleha Mustafa ◽  
Zurina Shamsudin

This research aims to determine the effect of silver nanoparticles concentrations as antimicrobial coatings when doped to TiO2 coatings. The TiO2 coatings were prepared by sol–gel method initiating Titanium Isopropoxide–Propanol mixture as a precursor solution. The silver nanoparticles (40 nm) were then doped to the coating after sintering at 500°C. Two concentrations of silver nanoparticles, (50 ppm and 1000 ppm), were prepared for comparison in this study. Microstructure and crystalline phase of coatings were evaluated using Scanning Electron Microscope (SEM) and Glancing Angle X-Ray Difraction (GAXRD) technique. The antibacterial test was according to McFarland standard for detecting E.Coli, S.Aerues, fungas and Methicillin-Resistant Staphylococcus Aureus (MRSA). Results show that only coatings with the concentrations of 1000 ppm of silver nanoparticle function as antimicrobial coatings.

Arena Tekstil ◽  
2013 ◽  
Vol 28 (1) ◽  
Author(s):  
Maya Komalasari ◽  
Bambang Sunendar

Partikel nano TiO2 berbasis air dengan pH basa telah berhasil disintesis dengan menggunakan metode sol-gel dan diimobilisasi pada kain kapas dengan menggunakan kitosan sebagai zat pengikat silang. Sintesis dilakukan  dengan prekursor TiCl4 pada konsentrasi 0,3 M, 0,5 M dan 1 M, dan menggunakan templat kanji dengan proses kalsinasi pada suhu 500˚C selama 2 jam. Partikel nano TiO2 diaplikasikan ke kain kapas dengan metoda pad-dry-cure dan menggunakan kitosan sebagai crosslinking agent. Berdasarkan hasil Scanning Electron Microscope (SEM),diketahui bahwa morfologi partikel TiO2 berbentuk spherical dengan ukuran nano (kurang dari 100 nm). Karakterisasi X-Ray Diffraction (XRD) menunjukkan adanya tiga tipe struktur kristal utama, yaitu (100), (101) dan (102) dengan fasa kristal yang terbentuk adalah anatase dan rutile. Pada karakterisasi menggunakan SEM terhadap serbuk dari TiO2 yang telah diaplikasikan ke permukaan kain kapas, terlihat adanya imobilisasi partikel nano TiO2 melalui ikatan hidrogen silang dengan kitosan pada kain kapas. Hasil analisa tersebut kemudian dikonfirmasi dengan FTIR (Fourier Transform Infra Red) yang hasilnya memperlihatkan puncak serapan pada bilangan gelombang 3495 cm-1, 2546 cm-1, dan 511 cm-1,  yang masing-masing diasumsikan sebagai adanya vibrasi gugus fungsi O-H, N-H dan Ti-O-Ti. Hasil SEM menunjukkan pula bahwa kristal nano yang terbentuk diantaranya adalah fasa rutile , yang berdasarkan literatur terbukti dapatberfungsi sebagai anti UV.


2006 ◽  
Vol 514-516 ◽  
pp. 1155-1160 ◽  
Author(s):  
Talaat Moussa Hammad

Sol gel indium tin oxide thin films (In: Sn = 90:10) were prepared by the sol-gel dipcoating process on silicon buffer substrate. The precursor solution was prepared by mixing SnCl2.2H2O and InCl3 dissolved in ethanol and acetic acid. The crystalline structure and grain orientation of ITO films were determined by X-ray diffraction. The surface morphology of the films was characterized by scanning electron microscope (SEM). Optical transmission and reflectance spectra of the films were analyzed by using a UV-visible spectrophotometer. The transport properties of majority charge carriers for these films were studied by Hall measurement. ITO thin film with electrical resistivity of 7.6 ×10-3 3.cm, Hall mobility of approximately 2 cm2(Vs)-1 and free carrier concentration of approximately 4.2 ×1020 cm-3 are obtained for films 100 nm thick films. The I-V curve measurement showed typical I-V characteristic behavior of sol gel ITO thin films.


2015 ◽  
Vol 33 (4) ◽  
pp. 714-718 ◽  
Author(s):  
Neeraj K. Mishra ◽  
Chaitnaya Kumar ◽  
Amit Kumar ◽  
Manish Kumar ◽  
Pratibha Chaudhary ◽  
...  

AbstractA nanocomposite of 0.5SnO2–0.5Al2O3 has been synthesized using a sol-gel route. Structural and optical properties of the nanocomposite have been discussed in detail. Powder X-ray diffraction and scanning electron microscopy with energy-dispersive X-ray diffraction spectroscopy confirm the phase purity and the particle size of the 0.5SnO2–0.5Al2O3 nanocomposite (13 to 15 nm). The scanning electron microscopy also confirms the porosity in the sample, useful in sensing applications. The FT-IR analysis confirms the presence of physical interaction between SnO2 and Al2O3 due to the slight shifting and broadening of characteristic bands. The UV-Vis analysis confirms the semiconducting nature because of direct transition of electrons into the 0.5SnO2–0.5Al2O3 nanocomposites.


2007 ◽  
Vol 336-338 ◽  
pp. 1914-1917
Author(s):  
Lei Yang ◽  
Zhen Yi Zhang ◽  
Xiao Shan Ning ◽  
Guang He Li

In this paper, a novel and highly efficient hydroxyapatite (HA) carrier for cultivating hydrocarbon degradation bacteria (HDB) is introduced. The HA particles synthesized through a sol-gel method and different heat treatments were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and BET method. The microbial amount and activities of HDB cultivated on HA carriers were quantitatively investigated in order to assess their enriching capabilities. The results showed that HA synthesized at 550°C and the one without calcination could enrich HDB 3 and 2 magnitude orders more than the activated carbon, respectively. Mechanisms of bacterial enrichment on HA and activated carbon were also studied, and it is believed that the high bioactivity and the surface morphology of HA were responsible for the efficient reproduction of HDB. It is concluded that HA is a potential candidate to replace the conventionally used activated carbon as a novel carrier applied in the filed of bioremediation for oil contaminated soil.


2021 ◽  
Vol 66 (1) ◽  
pp. 57-64
Author(s):  
Hang Pham Vu Bich ◽  
Yen Nguyen Hai ◽  
Mai Phung Thi Thanh ◽  
Dung Dang Duc ◽  
Hung Nguyen Manh ◽  
...  

In this study, we present the process of synthesis FexNi1-xMn2O4 (x = 0; 0.1; 0.3; 0.5; 0.7; 0.9; 1) by method sol-gel. Scanning electron microscope results shows that the particle size is about 50 nm. The X-ray diffraction diagram shows that the samples are single phase, changing structure clearly as the x ratio increases from 0 to 1. The lattice constant, the bond length also changes with x-value as shown on the Raman scattering spectrum. The results of the vibrating sample magnetometer show that the magnetism of the material FexNi1-xMn2O4 changes with the value of x and reaches a maximum in the range x from 0.5 to 0.7.


2012 ◽  
Vol 476-478 ◽  
pp. 2059-2062
Author(s):  
Chen Wang ◽  
Ya Dong Li ◽  
Gu Qiao Ding

Tributyl borate was first adopted for the introduction of boron in the preparation of bioactive borosilicate xerogel by sol-gel method. The xerogel reacted continuously in 0.25M K2HPO4 solution with a starting pH value of 7.0 at 37 °C for 1day. The structural, morphologies and compositional changes resulting from the conversion were characterized using X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. The results indicated that speed of formation of HA was cut way back on the time with the addition of boron and the induction period for the HA nucleation on the surface of the borosilicate xerogel was short than 1 days. The conversion mechanism of the borosilicate xerogels to hydroxyapaptite was also discussed.


2020 ◽  
Vol 11 (4) ◽  
pp. 5382-5387
Author(s):  
Irshad Ul Haq Bhat ◽  
Maisarah Binti Alias

The approach towards green synthetic methods has been enormously encouraged to synthesise nanoparticles for various uses. In this study, the one-pot synthetic method was adapted to synthesise silver nanoparticles (AgNPs) using Melastoma malabathricum (M. malabathricum) aqueous extract. The formation of AgNPs was confirmed by observing the results obtained by optical characterisation methods. The plasma resonance band along with shoulder at 375 nm and 595 nm, respectively, in Uv-Visible spectra supported the conversion of silver (Ag) to AgNPs reduced by functional groups present in the plant extract. The size of AgNPs was 31 nm and cubic in shape as confirmed by X-ray diffractometry (XRD) using Scherer equation. X-Ray Fluorescence (XRF) results also confirmed the presence of silver. The FTIR characterisation confirmed the presence of reducing functional groups. The antibacterial activity of AgNPs against Staphylococcus aureus (S. aureus) was carried out by disc diffusion method with increasing concentration of AgNPs, and enhanced inhibition zone was observed. The AgNPs obtained can be further explored against different bacterial strains and can a potential candidate as an antibacterial agent using the green synthetic approach.


2019 ◽  
Vol 8 (1) ◽  
pp. 39 ◽  
Author(s):  
Susanto Susanto ◽  
Ricka Prasdiantika

Synthesis of Fe3O4@SiO2 modified with propyldiethylenetriamine (Fe3O4@SiO2@PDETA) with variation of synthesis routes have been investigated. Research was begun with synthesis of Fe3O4 using dispersion agent of trisodium citrate at coprecipitation system through stirring using ultrasonic wave. Coating magnetite with propyldiethylenetriamine modified silica was carried out through sol-gel process with two different mixing sequences of raw materials (two synthesis routes) with main materials of Fe3O4 synthesized, N-[3-(Trimethoxysilyl)propyl]-diethylenetriamine (TMSPDETA) and Na2SiO3. The products were characterized by fourier transform infrared (FTIR) spectrophotometer and scanning electron microscope-energy dispersive X-ray (SEM-EDX). Results indicate that Fe3O4@SiO2@PDETA has been synthesized succesfully. Fe3O4@SiO2@PDETA synthesized through route 1 (magnetite mixed with a mixture TMSPDETA and Na2SiO3) contains more propyldiethylenetriamine group than that of through route 2 (magnetite mixed with Na2SiO3 solution, then mixed with TMSPDETA)


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