Preparation of Straight and Orderly Polypyrrole Microrods through Soft Template Methods

2011 ◽  
Vol 306-307 ◽  
pp. 679-683
Author(s):  
Li Bo Sun ◽  
Yuan Chang Shi ◽  
Lin Ya Chu ◽  
Bing Chang Zhang ◽  
Jiu Rong Liu

The straight and orderly microrods of polypyrrole(PPy) was synthesized in a microemulsion system consisted of cetyltrimethylammonium bromide(CTAB), n-pentanol, water and pyrrole by chemical oxidative polymerization, in which CTAB was used as soft templates and APS was used as the oxidant. Fourier-transform infrared spectroscopy (FTIR) was used to characterize the structure of the PPy microrods. Transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM) was used to characterize the morphology of the samples. We discussed the impact of temperature, the adding way of the oxidant, the amount of cosurfactant n-pentanol to the morphology of PPy microrods. The results showed that straight and orderly PPy microrods with a diameter about 300nm and a length up to 20μm were synthesized when the temperature was kept at room temperature (25°C), the dropping time of APS was more than 1.5h, the ratio of CTAB to n-pentanol was 0.6:1, and the polymerization time was about 24h. We studied the growth process of PPy microrods by HTEM analysis. HTEM images revealed that the growth process of PPy changed from hollow microrods, semi-hollow microrods, and finally solid microrods.

2011 ◽  
Vol 364 ◽  
pp. 278-282
Author(s):  
Rida Tajau ◽  
Dahlan Khairul Mohd. Zaman ◽  
Mohd Hilmi Mahmood ◽  
Wan Md Zin Wan Yunus ◽  
Hashim Kamaruddin

In this study, we report the preparation of Acrylated Palm Oil (APO) nanoparticles using aqueous Cetyltrimethylammonium bromide (CTAB) microemulsion system. This microemulsion system which contains the dispersed APO nanodroplets was subjected to the gamma irradiation to induce the formation of the crosslinked APO nanoparticles. The dynamic light scattering (DLS), the Fourier Transform Infrared (FTIR) spectrocospy and the Transmission Electron Microscopy (TEM) were used to characterize the size and the chemical structure of the nanoparticle. Sized of the APO nanoor microparticle can be varied depended on the volumes of the modified palm oil and the irradiation doses. Their size is in the range of 73 to 100 nanometer (nm) after irradiation using gamma irradiator. This radiation-induced method provides a free initiator induced and easy to control process as compared to the classical or chemical initiator process.


Author(s):  
A.J. Tousimis ◽  
T.R. Padden

The size, shape and surface morphology of human erythrocytes (RBC) were examined by scanning electron microscopy (SEM), of the fixed material directly and by transmission electron microscopy (TEM) of surface replicas to compare the relative merits of these two observational procedures for this type specimen.A sample of human blood was fixed in glutaraldehyde and washed in distilled water by centrifugation. The washed RBC's were spread on freshly cleaved mica and on aluminum coated microscope slides and then air dried at room temperature. The SEM specimens were rotary coated with 150Å of 60:40- gold:palladium alloy in a vacuum evaporator using a new combination spinning and tilting device. The TEM specimens were preshadowed with platinum and then rotary coated with carbon in the same device. After stripping the RBC-Pt-C composite film, the RBC's were dissolved in 2.5N HNO3 followed by 0.2N NaOH leaving the preshadowed surface replicas showing positive topography.


Author(s):  
S. Mahajan

The evolution of dislocation channels in irradiated metals during deformation can be envisaged to occur in three stages: (i) formation of embryonic cluster free regions, (ii) growth of these regions into microscopically observable channels and (iii) termination of their growth due to the accumulation of dislocation damage. The first two stages are particularly intriguing, and we have attempted to follow the early stages of channel formation in polycrystalline molybdenum, irradiated to 5×1019 n. cm−2 (E > 1 Mev) at the reactor ambient temperature (∼ 60°C), using transmission electron microscopy. The irradiated samples were strained, at room temperature, up to the macroscopic yield point.Figure 1 illustrates the early stages of channel formation. The observations suggest that the cluster free regions, such as A, B and C, form in isolated packets, which could subsequently link-up to evolve a channel.


Author(s):  
A.C. Daykin ◽  
C.J. Kiely ◽  
R.C. Pond ◽  
J.L. Batstone

When CoSi2 is grown onto a Si(111) surface it can form in two distinct orientations. A-type CoSi2 has the same orientation as the Si substrate and B-type is rotated by 180° degrees about the [111] surface normal.One method of producing epitaxial CoSi2 is to deposit Co at room temperature and anneal to 650°C.If greater than 10Å of Co is deposited then both A and B-type CoSi2 form via a number of intermediate silicides .The literature suggests that the co-existence of A and B-type CoSi2 is in some way linked to these intermediate silicides analogous to the NiSi2/Si(111) system. The phase which forms prior to complete CoSi2 formation is CoSi. This paper is a crystallographic analysis of the CoSi2/Si(l11) bicrystal using a theoretical method developed by Pond. Transmission electron microscopy (TEM) has been used to verify the theoretical predictions and to characterise the defect structure at the interface.


Author(s):  
Kazue Nishimoto ◽  
Miki Muraki ◽  
Ryuji Tamura

AbstractTernary Ag–In–(Eu, Ce) 1/1 approximants are synthesized and their structures are studied by transmission electron microscopy (TEM). For both the approximants, superlattice spots are clearly observed at room temperature, and the superstructures of the Ag–In–(Eu, Ce) approximants are found to be similar to those of Cd


2011 ◽  
Vol 287-290 ◽  
pp. 96-99 ◽  
Author(s):  
Xian Biao Wang ◽  
Jin Liu ◽  
Dong Lin Zhao ◽  
Xiao Jie Song

FeS nanoparticles with uniform size have been prepared through a facile route using (sodium carboxymethyl cellulose) CMC as soft template. The nanoparticles are about 4-6 nm by observation of transmission electron microscopy (TEM). The CMC template could also stabilize the FeS nanoparticles and resist aggregation. It is important to note that the size of nanoparticles can be easily controlled by the concentration of iron and sulfur source during the synthetic process. Interestingly, the FeS nanoparticles could assemble into rod-like morphology at higher concentration. More importantly, the CMC-stabilized FeS nanoparticles exibit enhanced performance for Cr(Ⅵ) removal as compared with FeS synthesized without CMC stabilizer.


2016 ◽  
Vol 874 ◽  
pp. 323-327
Author(s):  
Hong Xiu Zhou ◽  
Ming Lei Li ◽  
Neng Dong Duan ◽  
Bo Wang ◽  
Zhi Feng Shi ◽  
...  

A nanotwinned surface is formed on a titanium alloy under nanoindentations. Prior to nanoindentation, blocks of a ternary titanium alloy are machined by chemical mechanical polishing. The surface roughness Ra and peak-to-valley values are 1.135 nm and 8.82 nm, respectively. The hardness in the indented surface is greatly increased, indicated from the load-displacement curves compared to the polished surfaces. Nanotwins are confirmed using transmission electron microscopy. The nanotwinned surface is uniformly generated by nanoindentations at room temperature, which is different from previous findings, in which high temperature, high pressure, or chemical reagents are usually used. The nanotwinned surface is produced by pure mechanical stress, neither material removal nor addition.


2010 ◽  
Vol 16 (S2) ◽  
pp. 122-123
Author(s):  
P Specht ◽  
R Gulotty ◽  
D Barton ◽  
R Cieslinski ◽  
S Rozeveld ◽  
...  

Extended abstract of a paper presented at Microscopy and Microanalysis 2010 in Portland, Oregon, USA, August 1 – August 5, 2010.


2019 ◽  
Vol 55 (27) ◽  
pp. 3876-3878 ◽  
Author(s):  
Eleonora Aneggi ◽  
Jordi Llorca ◽  
Alessandro Trovarelli ◽  
Mimoun Aouine ◽  
Philippe Vernoux

In situ environmental transmission electron microscopy discloses room temperature carbon soot oxidation by ceria–zirconia at the nanoscale.


2019 ◽  
Vol 107 (8) ◽  
pp. 725-735
Author(s):  
Hoda H. Saleh ◽  
Rehab Sokary ◽  
Zakaria I. Ali

Abstract Polyaniline (PANI) nanoparticles and PANI/poly vinyl alcohol (PVA) nanocomposite films were synthesized by the oxidative polymerization of aniline and ammonium peroxodisulfate (APS), as an oxidizing agent in aqueous medium. The PANI/PVA nanocomposite films were exposed to γ-irradiation after oxidative polymerization. Synthesized polyaniline (PANI) nanoparticles and PANI/PVA nanocomposite films were characterized by attenuated total reflectance infrared spectroscopy (FTIR-ATR), X-ray diffraction, high resolution scanning electron microscopy, (HRSEM) high resolution transmission electron microscopy, (HRTEM) and UV-VIS absorption spectroscopy. Energy band gap of PANI nanofibers was determined from Tauc’s plots which equal 4.2 eV. Scanning electron microscopy images show that chemically synthesized of polyaniline has nanofibers structure and irradiated PANI/PVA nanocomposite have a mixture of nanorod and nanosphere structures. The transmission electron microscopy show that chemically synthesized of polyaniline has average length in the range 34 ± 10 nm with less wide distribution, where as the irradiated PANI/PVA nanocomposite has coreshell structure.


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