New amphiphilic sulfonic acid dopant-cum-templates for diverse conducting polyaniline nanomaterials

2012 ◽  
Vol 127 (3) ◽  
pp. 1781-1793 ◽  
Author(s):  
Shekhar D. Shinde ◽  
M. Jayakannan
e-Polymers ◽  
2007 ◽  
Vol 7 (1) ◽  
Author(s):  
Wu Yan ◽  
Xing Shuangxi ◽  
Jing Shengyu ◽  
Zhou Teili ◽  
Zhao Chun

AbstractWe reported a chemical approach for the in-situ preparation of conducting polyaniline (PANI)/Fe2O3 composite dispersions using dodecylbenzene sulfonic (DBSA) acid both as dopant and surfactant. The PANI/Fe2O3 composite dispersions were characterized by X-ray diffraction, UV-vis and FT-IR spectra and conductivity measurement. The dispersions showed good stability and existed without precipitate for at least half a year. The gas-sensing behavior of the composite film to 100 ppm of NH3 was studied through monitoring the change of the resistance.


Author(s):  
E. S. Boatman ◽  
G. E. Kenny

Information concerning the morphology and replication of organism of the family Mycoplasmataceae remains, despite over 70 years of study, highly controversial. Due to their small size observations by light microscopy have not been rewarding. Furthermore, not only are these organisms extremely pleomorphic but their morphology also changes according to growth phase. This study deals with the morphological aspects of M. pneumoniae strain 3546 in relation to growth, interaction with HeLa cells and possible mechanisms of replication.The organisms were grown aerobically at 37°C in a soy peptone yeast dialysate medium supplemented with 12% gamma-globulin free horse serum. The medium was buffered at pH 7.3 with TES [N-tris (hyroxymethyl) methyl-2-aminoethane sulfonic acid] at 10mM concentration. The inoculum, an actively growing culture, was filtered through a 0.5 μm polycarbonate “nuclepore” filter to prevent transfer of all but the smallest aggregates. Growth was assessed at specific periods by colony counts and 800 ml samples of organisms were fixed in situ with 2.5% glutaraldehyde for 3 hrs. at 4°C. Washed cells for sectioning were post-fixed in 0.8% OSO4 in veronal-acetate buffer pH 6.1 for 1 hr. at 21°C. HeLa cells were infected with a filtered inoculum of M. pneumoniae and incubated for 9 days in Leighton tubes with coverslips. The cells were then removed and processed for electron microscopy.


2020 ◽  
Author(s):  
Adam Bruce Ung ◽  
G. K. Surya Prakash ◽  
Thieo E. Hogen-Esch

2020 ◽  
Author(s):  
Adam Bruce Ung ◽  
G. K. Surya Prakash ◽  
Thieo E. Hogen-Esch ◽  
Adam Bruce Ung

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