Incubation of PbSe Thin Films in a Tin(II) Salt Aqueous Solution: Modification and Ion-Exchange Reactions

2015 ◽  
Vol 31 (8) ◽  
pp. 790-797 ◽  
Author(s):  
Zinaida I. Smirnova ◽  
Larisa N. Maskaeva ◽  
Vyacheslav F. Markov ◽  
Vladimir I. Voronin ◽  
Mikhail V. Kuznetsov
2016 ◽  
Vol 45 (43) ◽  
pp. 17312-17318 ◽  
Author(s):  
Eun-Kyung Kim ◽  
Dasom Park ◽  
Nabeen K. Shrestha ◽  
Jinho Chang ◽  
Cheol-Woo Yi ◽  
...  

An aqueous solution based synthetic method for binder-free Ag2Te thin films using ion exchange induced chemical transformation of Ag/AgxO thin films.


2018 ◽  
Vol 9 (23) ◽  
pp. 6750-6754 ◽  
Author(s):  
Alessandro Greco ◽  
Alexander Hinderhofer ◽  
M. Ibrahim Dar ◽  
Neha Arora ◽  
Jan Hagenlocher ◽  
...  

1986 ◽  
Vol 75 ◽  
Author(s):  
T. J. Cumberbatch ◽  
P. E. Barden ◽  
J. Knightley

AbstractA CO2 laser, operating at 10.6μm, has been used to promote the growth of topotaxial layers of the chalcocite phase of cuprous sulphide in cadmium sulphide thin films immersed in an organic solution of a cuprous salt at ambient temperature. Cuprous sulphide growth is initiated by the laser beam which passes through the liquid and raises the surface temperature of the CdS allowing ion exchange to take place without changing the surface topography. An investigation into different combinations of organic solvents and cuprous/cupric salts has revealed that cuprous iodide in acetonitrile or propionitrile yields the fastest growth rates. The results are compared with those obtained from junctions fabricated using lasers operating in the visible frequency range.


ChemInform ◽  
2010 ◽  
Vol 25 (6) ◽  
pp. no-no
Author(s):  
M. T. S. NAIR ◽  
P. K. NAIR ◽  
H. M. K. K. PATHIRANA ◽  
R. A. ZINGARO ◽  
E. A. MEYERS

1993 ◽  
Vol 140 (10) ◽  
pp. 2987-2994 ◽  
Author(s):  
M. T. S. Nair ◽  
P. K. Nair ◽  
H. M. K. K. Pathirana ◽  
Ralph A. Zingaro ◽  
Edward A. Meyers

2009 ◽  
Vol 255 (18) ◽  
pp. 8158-8163 ◽  
Author(s):  
Ramphal Sharma ◽  
Anil Ghule ◽  
Vidya Taur ◽  
R. Joshi ◽  
Rajaram Mane ◽  
...  

2002 ◽  
Vol 755 ◽  
Author(s):  
Buddhimathie Jayasekera ◽  
Stephanie L. Brock

ABSTRACTA variety of ion exchange techniques for Cu2P3I2 and its mixed pnictogen analog Cu2P1.8As1.2I2 have been studied. Ag2P3I2 is an existing material, previously prepared from Cu2P3I2 by ion exchange of Ag+ for Cu+ in aqueous medium. This method is compared to non-aqueous (ionic liquid) and solid state routes for ion exchange. Additionally, the new compound Ag2P1.8As1.2I2 with cell parameters a = 15.838(17) Å, b = 13.684(10) Å, c = 15.580(17) Å and β = 117.63(7)°, has been prepared by reaction of Cu2P1.8As1.2I2 with AgNO3 in aqueous solution.


2020 ◽  
Vol 16 ◽  
Author(s):  
Reda M. El-Shishtawy ◽  
Abdullah M. Asiri ◽  
Nahed S. E. Ahmed

Background: Color effluents generated from the production industry of dyes and pigments and their use in different applications such as textile, paper, leather tanning, and food industries, are high in color and contaminants that damage the aquatic life. It is estimated that about 105 of various commercial dyes and pigments amounted to 7×105 tons are produced annually worldwide. Ultimately, about 10–15% is wasted into the effluents of the textile industry. Chitin is abundant in nature, and it is a linear biopolymer containing acetamido and hydroxyl groups amenable to render it atmospheric by introducing amino and carboxyl groups, hence able to remove different classes of toxic organic dyes from colored effluents. Methods: Chitin was chemically modified to render it amphoteric via the introduction of carboxyl and amino groups. The amphoteric chitin has been fully characterized by FTIR, TGA-DTG, elemental analysis, SEM, and point of zero charge. Adsorption optimization for both anionic and cationic dyes was made by batch adsorption method, and the conditions obtained were used for studying the kinetics and thermodynamics of adsorption. Results: The results of dye removal proved that the adsorbent was proven effective in removing both anionic and cationic dyes (Acid Red 1 and methylene blue (MB)), at their respective optimum pHs (2 for acid and 8 for cationic dye). The equilibrium isotherm at room temperature fitted the Freundlich model for MB, and the maximum adsorption capacity was 98.2 mg/g using 50 mg/l of MB, whereas the equilibrium isotherm fitted the Freundlich and Langmuir model for AR1 and the maximum adsorption capacity was 128.2 mg/g. Kinetic results indicate that the adsorption is a two-step diffusion process for both dyes as indicated by the values of the initial adsorption factor (Ri) and follows the pseudo-second-order kinetics. Also, thermodynamic calculations suggest that the adsorption of AR1 on the amphoteric chitin is an endothermic process from 294 to 303 K. The result indicated that the mechanism of adsorption is chemisorption via an ion-exchange process. Also, recycling of the adsorbent was easy, and its reuse for dye removal was effective. Conclusion: New amphoteric chitin has been successfully synthesized and characterized. This resin material, which contains amino and carboxyl groups, is novel as such chemical modification of chitin hasn’t been reported. The amphoteric chitin has proven effective in decolorizing aqueous solution from anionic and cationic dyes. The adsorption behavior of amphoteric chitin is believed to follow chemical adsorption with an ion-exchange process. The recycling process for few cycles indicated that the loaded adsorbent could be regenerated by simple treatment and retested for removing anionic and cationic dyes without any loss in the adsorbability. Therefore, the study introduces a new and easy approach for the development of amphoteric adsorbent for application in the removal of different dyes from aqueous solutions.


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