A non-enzymatic electrochemical approach for l-lactic acid sensor development based on CuO·MWCNT nanocomposites modified with a Nafion matrix

2020 ◽  
Vol 44 (23) ◽  
pp. 9775-9787 ◽  
Author(s):  
Mohammad Musarraf Hussain ◽  
Abdullah M. Asiri ◽  
Mohammed M. Rahman

Copper oxide decorated multi-walled carbon nanotube nanocomposites (CuO·MWCNT NCs) were prepared using a simple wet-chemical technique in basic medium.

RSC Advances ◽  
2016 ◽  
Vol 6 (70) ◽  
pp. 65338-65348 ◽  
Author(s):  
Mohammed M. Rahman ◽  
Mohammad Musarraf Hussain ◽  
Abdullah M. Asiri

Strontium oxide nanoparticle decorated carbon nanotube nanocomposites (SrO·CNT NCs) were prepared in alkaline medium using a wet-chemical technique at low temperature.


RSC Advances ◽  
2017 ◽  
Vol 7 (24) ◽  
pp. 14649-14659 ◽  
Author(s):  
Mohammed M. Rahman ◽  
Jahir Ahmed ◽  
Abdullah M. Asiri

γ-Ce2S3-decorated multi-walled carbon nanotube nanocomposite (Ce2S3-CNT NC) was synthesized by a wet chemical method in basic media.


RSC Advances ◽  
2019 ◽  
Vol 9 (54) ◽  
pp. 31670-31682 ◽  
Author(s):  
Mohammed M. Rahman ◽  
Mohammad Musarraf Hussain ◽  
Abdullah M. Asiri

A simple wet-chemical technique was used to prepare zinc oxide-doped vanadium pentaoxide nanorods (ZnO·V2O5 NRs) in an alkaline environment.


2020 ◽  
Vol 12 (27) ◽  
pp. 3470-3483 ◽  
Author(s):  
Mohammed M. Rahman ◽  
Tahir Ali Sheikh ◽  
Abdullah M. Asiri ◽  
K. A. Alamry ◽  
M. A. Hasnat

Semiconductor doped Zn-doped Er2O3 nano-composite materials were prepared via a wet-chemical technique in a single-step at alkaline pH to develop a selective and sensitive para-nitrophenol capturing electrochemical probe for environmental remediation.


2006 ◽  
Vol 972 ◽  
Author(s):  
Atmane Ait-Salah ◽  
Chintalapalle V Ramana ◽  
François Gendron ◽  
Jean-François Morhange ◽  
Alain Mauger ◽  
...  

AbstractWe present the synthesis and characterization of a novel lithium iron polyphosphate LiFe2P3O10 prepared by wet-chemical technique from nitrate precursors. The crystal system is shown to be monoclinic (P21/m space group) and the refined cell parameters are a=4.596 Å, b=8.566 Å, c=9.051 Å and β=97.46°. LiFe2P3O10 has a weak antiferromagnetic ordering below the Néel temperature TN=19 K. Electrochemical measurements carried out at 25 °C in lithium cell with LiPF6-EC-DEC electrolyte show a capacity 70 mAh/g in the voltage range 2.7-3.9 V.


2021 ◽  
Vol 878 ◽  
pp. 73-80
Author(s):  
Khansaa Al-Essa ◽  
A V Radha ◽  
Alexandra Navrotsky

The nanoscale, cubic silver (I) oxide (Ag2O.nH2O) with different particles sizes and surface areas were synthesized by a wet chemical technique. The prepared crystallite size ranges were from (33.3±0.3 to 39.4±0.4 nm). Interface areas were estimated by comparing the surface areas measured by N2 adsorption to the crystallite sizes refined from X-ray diffraction data. The interface enthalpy of Ag2O.nH2O nanocrystal was measured using isothermal acid solution calorimetry in 25%HNO3 at 26°C. The interface enthalpy was verified by utilizing thermodynamic cycle. The enthalpies of drop solution (ΔHds) for Ag2O.nH2O are exothermic and range from (-62.228±0.197) to (-64.025±0.434 kJ/mol), while its interface enthalpy is (0.842±0.508 J/m2). This work provides the first calorimetric measurement of the interface enthalpy of nanocrystalline silver (I) oxide (Ag2O.nH2O).


2020 ◽  
Vol 46 (17) ◽  
pp. 26675-26681 ◽  
Author(s):  
Hira ◽  
Aysha Daud ◽  
Sonia Zulfiqar ◽  
Philips O. Agboola ◽  
Imran Shakir ◽  
...  

1971 ◽  
Vol 25 (6) ◽  
pp. 668-671 ◽  
Author(s):  
Gerald S. Golden

Iron analyses performed on used gas turbine lubricating oil samples by several variations of rotating disk–spark emission spectrography, atomic absorptiometry, and x-ray fluorescence spectrometry are compared with a quantitative wet chemical technique. The results indicate that emission spectrography with a cobalt internal standard, atomic absorptiometry with a nitrous oxide–acetylene flame, and x-ray fluorescence, both dispersive and nondispersive, are the most reliable instrumental methods. The iron contained in the samples exists primarily as particulates 1 µ or less in diameter.


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