DyCrxFe(1-x)O3 nanoparticles prepared by wet chemical technique for photocatalytic applications

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


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.


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.


2020 ◽  
Vol 10 (19) ◽  
pp. 6670
Author(s):  
Denis O’Sullivan ◽  
Hazel McArdle ◽  
Sing Wei Ng ◽  
Paula Bourke ◽  
Robert Forster ◽  
...  

Collagen coatings were applied onto polystyrene microplates using a cold atmospheric pressure plasma process. The coatings were compared to standard wet chemical collagen thin films using microscopy, surface energy, infra-red spectroscopy, electrophoresis, and cell culture techniques. Thin films were also deposited on gold electrodes using both coating methods and their structural and barrier properties probed using cyclic voltammetry. While the wet chemical technique produced a thicker deposit, both films appear equivalent in terms of coverage, porosity, structure, and chemistry. Significantly, the cold plasma method preserves both the primary and secondary structure of the protein and this results in high biocompatibility and cell activity that is at least equivalent to the standard wet chemical technique. The significance of these results is discussed in relation to the benefits of a single step plasma coating in comparison to the traditional multi-step aseptic coating technique.


2014 ◽  
Vol 911 ◽  
pp. 410-414
Author(s):  
Farah Diana Mohd Daud ◽  
Srimala Sreekantan ◽  
Abdul Rahman Mohamed

CO2 is the major anthropogenic greenhouse gas which contributes to the increasing atmospheric CO2 concentration, leading to serious global warming and climate change. Thus, the present paper investigates the CO2-capture performance of synthesized calcium hydroxides, Ca (OH)2nanosorbent at intermediate-high temperatures which are 350, 450, 550 and 650oC. CO2 adsorption performance was analysed by thermo-gravimetricanalyser (TGA).The CO2 adsorption temperature strongly influenced the capture performance of the sorbent.Facile wet chemical technique was utilized to synthesize Ca (OH)2 nanorod sorbent structures using calcium nitrate tetrahydrate, Ca (NO3)2.4H2O as the calcium precursor, and precipitated with sodium hydroxides (NaOH) in N,N-Dimethylformamide (DMF) mixed deionized (DI) water media at 55 oC. X-ray diffraction (XRD) result exhibitedCa (OH)2hexagonal crystal structures. The Ca (OH)2 particle size and morphological properties before and after CO2 adsorption are studied by Field Emission Scanning Electron Microscopy (FESEM). The FESEM image indeed showed the rod like shape of Ca (OH)2nanosorbent with rod length approximately700 nm while the diameter 140nm. When CO2 molecules were adsorbed by Ca (OH)2nanosorbent, the nanorodstructures are changed to rigid interconnected each other like a lump shaped. Ca (OH)2nanosorbentseems to be a potentially good absorbent for capturing CO2when increased temperatures. However, at intermediate temperature 350 and 450oC, the synthesized Ca (OH)2nanosorbent demonstrated higher CO2 adsorption (141 to 220 mg/g CO2) than others intermediate temperature CO2 sorbent such as layer double hydroxides (LDH), lithium zirconates (LiZrO3) and hydrotalcite.


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