Development of a potential LPG sensor based on a PANI–Co3O4 nanocomposite that functions at room temperature

2019 ◽  
Vol 43 (44) ◽  
pp. 17340-17350 ◽  
Author(s):  
Neetu Singh ◽  
Prabhat Kumar Singh ◽  
Mridula Singh ◽  
Debraj Gangopadhyay ◽  
Saurabh Kumar Singh ◽  
...  

Nanostructured Co3O4 was synthesized by a sol–gel technique while 30% & 40% Co3O4–PANI (polyaniline) nanocomposites were successfully prepared employing an in situ polymerization technique.

Author(s):  
Abdu. I. Abdallah ◽  
M. Sayed ◽  
M. Awaad ◽  
Adam H. E. Yousif ◽  
S.M. Naga
Keyword(s):  
Sol Gel ◽  

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Oon Lee Kang ◽  
Azizan Ahmad ◽  
Nur Hasyareeda Hassan ◽  
Usman Ali Rana

In the present research, [MG49-LiClO4]:[HNO3-THF/TiO2-SiO2] and [MG49-LiClO4]:[ClHNO2-THF/TiO2-SiO2] polymer electrolytes were first prepared through simple stepwise in situ techniques: sol-gel technique and solution-cast technique. [MG49-LiClO4]:[HNO3-THF/TiO2-SiO2] and [MG49-LiClO4]:[ClHNO2-THF/TiO2-SiO2] polymer electrolytes were then characterized through different experimental techniques. [MG49-LiClO4]:[HNO3-THF/TiO2-SiO2] and [MG49-LiClO4]:[ClHNO2-THF/TiO2-SiO2] polymer electrolytes had exhibited significant structural changes upon different salt concentrations. In the present investigation, [MG49-LiClO4]:[HNO3-THF/TiO2-SiO2] and [MG49-LiClO4]:[ClHNO2-THF/TiO2-SiO2] polymer electrolytes had attained maximum ionic conductivities (σ~10-7 S/cm at ambient temperature; 10−4 S/cm at 100°C) upon 25 wt.% salt insertion. [MG49-LiClO4]:[HNO3-THF/TiO2-SiO2] and [MG49-LiClO4]:[ClHNO2-THF/TiO2-SiO2] polymer electrolytes had exhibited distinct conduction mechanisms in similar experimental configuration. [MG49-LiClO4]:[HNO3-THF/TiO2-SiO2] and [MG49-LiClO4]:[ClHNO2-THF/TiO2-SiO2] polymer electrolytes had exhibited different stability characteristics over certain operational condition.


2019 ◽  
Vol 33 (13) ◽  
pp. 1950134 ◽  
Author(s):  
Muhammad Ajmal ◽  
M. U. Islam

Y-type hexagonal ferrite (CaBaCo2Ga[Formula: see text]Fe[Formula: see text]O[Formula: see text]) was synthesized by sol–gel technique. The ferrite–polymer composites (1−x)CaBaCo2Ga[Formula: see text]Fe[Formula: see text]O[Formula: see text]+(x)polyaniline (x=0.25, 0.50, 0.75, 1) namely PF1, PF2, PF3 and polyaniline (PANI) were synthesized by in situ polymerization. The synthesized samples were characterized by XRD, SEM, electrical and dielectric measurements, optical and magnetic studies. XRD pattern reveals a broad peak of polyaniline which is an indication of amorphous nature of PANI. Room-temperature resistivity increases from 2.14 × 101 [Formula: see text]cm to 2.78 × 10[Formula: see text]cm as ferrite content increases due to resistive behavior of the ferrite particles dispersed in the PANI matrix. The value of dielectric constant decreases at fixed frequency with increasing concentration of ferrite filler which is predominantly due to exchange of electrons between Fe[Formula: see text] and Fe[Formula: see text] ions that ultimately results in enhancement of electric polarization and conductivity. The optical bandgap increases with increasing amount of ferrite in the composites. The saturation magnetization and remanence increase with the increase of ferrite filler amount in PANI matrix whereas coercivity decreases. The decrease in coercivity and increase in saturation magnetization are related to Brown’s relation. The present nanocomposite samples may be the best candidates for electromagnetic shielding.


Polymer ◽  
2005 ◽  
Vol 46 (10) ◽  
pp. 3343-3354 ◽  
Author(s):  
Rajatendu Sengupta ◽  
Abhijit Bandyopadhyay ◽  
Sunil Sabharwal ◽  
Tapan K. Chaki ◽  
Anil K. Bhowmick

2000 ◽  
Vol 623 ◽  
Author(s):  
D.P. Eakin ◽  
M.G. Norton ◽  
D.F. Bahr

AbstractThin films of PZT were deposited onto platinized and bare single crystal NaCl using spin coating and sol-gel precursors. These films were then analyzed using in situ heating in a transmission electron microscope. The results of in situ heating are compared with those of an ex situ heat treatment in a standard furnace, mimicking the heat treatment given to entire wafers of these materials for use in MEMS and ferroelectric applications. Films are shown to transform from amorphous to nanocrystalline over the course of days when held at room temperature. While chemical variations are found between films crystallized in ambient conditions and films crystallized in the vacuum conditions of the microscope, the resulting crystal structures appear to be insensitive to these differences. Significant changes in crystal structure are found at 500°C, primarily the change from largely amorphous to the beginnings of clearly crystalline films. Crystallization does occur over the course of weeks at room temperature in these films. Structural changes are more modest in these films when heated in the TEM then those observed on actual wafers. The presence of Pt significantly influences both the resulting structure and morphology in both in situ and ex situ heated films. Without Pt present, the films appear to form small, 10 nm grains consisting of both cubic and tetragonal phases, whereas in the case of the Pt larger, 100 nm grains of a tetragonal phase are formed.


2013 ◽  
Vol 667 ◽  
pp. 265-271 ◽  
Author(s):  
Kevin Alvin Eswar ◽  
Azlinda Ab Aziz ◽  
Mohamad Rusop Mahmood ◽  
Saifollah Abdullah

Nanostructured ZnO as a seeded was prepared by sol-gel technique on p-type silicon in various low molarities. Zinc acetate, Diethanolamine (DEA), and isopropyl were use as starting material, stabilizer, and solvent respectively. Atomic Force Microscopy (AFM) analysis shows smooth surface and uniform layer were produced in low molarities of precursor. The surface morphology of nanostructured ZnO was analyzed by Field Emission Scanning Electron Microscopic (FESEM). It is found that the nanostructured ZnO were successfully deposited on the silicon substrate with size ~10 nm to ~35 nm. Photoluminescence spectroscopy was employed to study the band gap in room temperature. It shows that very low intensity of PL in 0.05m and 0.1 m. PL intensity become more obvious starting from 0.15 m of precursor concentration.


1999 ◽  
Vol 576 ◽  
Author(s):  
Khan M. Asif ◽  
M.I. Sarwar ◽  
Z. Ahmad

Novel micro-composites from Polyvinyl chloride (PVC) and silica were prepared using sol-gel technique. Different catalysts were used for the in-situ generation of silica network from tetraethylorthosilicate (TEOS) in the PVC matrix. Thin transparent films containing various proportions of silica in PVC were cast by the solvent elution technique. Mechanical properties of these films were studied. The results showed an increase in the value of Young's modulus and strain at rupture by the addition of small amount of silica in PVC. However, the stress at yields point and stress at rupture decreased with the addition of silica contents. Scanning electron microscopy (SEM-EDAX) studies were also performed on these samples.


2019 ◽  
Vol 15 (6) ◽  
pp. 350-356 ◽  
Author(s):  
Aline Matuella Moreira Ficanha ◽  
Angela Antunes ◽  
Carolina Elisa Demaman Oro ◽  
Alice Teresa Valduga ◽  
Cícero Matuella Moreira ◽  
...  

2010 ◽  
Vol 148-149 ◽  
pp. 1144-1147
Author(s):  
Xiang Rong Zhu ◽  
Lin Feng Lu ◽  
Hong Lie Shen

NixZn1-xFe2O4 (x=0.4, 0.6) powders are synthesized by sol-gel technique. The X-ray diffraction (XRD) measurements show their polycrystalline spinel structural characteristics. Both XRD and Atomic Force Microscopy demonstrate the samples are nanosized. At room temperature typical soft magnetism is exhibited by the samples. The reflection attenuation resulting from microwave absorption would reach to 1.9 dBm over the frequency range 6 GHz - 10 GHz when the samples are paved on a 10 cm  10 cm square aluminum plate with a thickness of about 0.35 mm.


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