scholarly journals Substitution of Ca2+ in Calcite by Sn2+ and Sr2+ cations through ion exchange characterized by X-ray absorption and photoelectron spectroscopies

MRS Advances ◽  
2021 ◽  
Author(s):  
Jonathan B. Junio ◽  
Prae Chirawatkul ◽  
Marlon T. Conato ◽  
Candy C. Mercado

AbstractTin (Sn2+) and strontium (Sr2+), two potential alternatives to lead (Pb2+) in perovskite formation, were explored in transforming calcium carbonate (CaCO3) into a leaving group in a cation exchange reaction. This is the first part of a sequential ion exchange process in transforming calcite into a Pb-free perovskite material for perovskite solar cell applications. Calcite, a polymorph of CaCO3, was successfully transformed into strontianite (SrCO3) through a cation exchange reaction. In the Sn substitution reaction on the other hand, no SnCO3 formation was noted. Instead, oxides of Sn were formed. The wider spaces in between Ca2+ cations in (100) orientation account for the higher atomic Sn2+ and Sr2+ concentrations as compared to (001) orientation, where the cation movement is restricted. X-ray absorption and photoelectron spectroscopies were used to investigate the ion-exchange transformation of calcite towards the formation of an intermediate carbonate material. Graphic abstract

Crystals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 162
Author(s):  
Ryan Taoran Wang ◽  
Elton Enchong Liu ◽  
Alex Fan Xu ◽  
Lory Wenjuan Yang ◽  
Jason Yuanzhe Chen ◽  
...  

Extra peaks have constantly been observed in the X-ray diffraction measurement for the CH3NH3PbI3 film. Such mysteries have now been uncovered in this paper, in which powder X-ray diffraction, in situ X-ray diffraction, and scanning electron microscopy measurements were conducted, and these peaks were attributed to the ethylammonium lead iodide (CH3CH2NH3PbI3/EAPbI3). It was found that the formation of EAPbI3 was triggered by the breakdown of N, N-dimethylformamide (DMF), which was adopted as the solvent in the preparation of the precursor solutions. EAPbI3 was generated by the organic cation exchange reaction in the subsequent annealing process. A simple solution for this problem is proposed in this paper as well, which would hopefully help the community to eradicate this impurity.


2015 ◽  
Vol 3 (35) ◽  
pp. 18279-18288 ◽  
Author(s):  
Amit K. Thakur ◽  
Murli Manohar ◽  
Vinod K. Shahi

Cross-linked poly(2-acrylamido-2-methyl-propanesulfonic acid) (PMPS)-based cation-exchange membranes (CEMs) were prepared, and the mono-valent selectivity of the membranes was significantly improved by a pore-sieving strategy using metal (copper) loading.


Clay Minerals ◽  
1973 ◽  
Vol 10 (2) ◽  
pp. 61-69 ◽  
Author(s):  
E. F. Vansant ◽  
J. B. Uytterhoeven

AbstractThe adsorption of organic ions derived from ammonium, containing aromatic and saturated rings, was studied using different techniques. The ions with acid character produced a complicated set of reactions including aluminium extraction, proton adsorption, a real ion-exchange with the organic ions and an excess adsorption of ammonium salts. With non-acidic compounds only a stoichiometric ion-exchange process was observed. X-ray diffraction and infrared spectroscopy were used to determine the orientation of the organic ions and to characterize the nature of the co-adsorbed organic material.


Nanoscale ◽  
2019 ◽  
Vol 11 (13) ◽  
pp. 5989-5997 ◽  
Author(s):  
Sampson Adjokatse ◽  
Hong-Hua Fang ◽  
Herman Duim ◽  
Maria Antonietta Loi

This study highlights the importance of a scalable blade coating technique and the ion exchange reaction in fabricating high-quality perovskite thin films.


1969 ◽  
Vol 24 (6) ◽  
pp. 900-902
Author(s):  
Kurt Bunzel

The selectivity coefficient K21 of an ion-exchange process is in general a function of the ionic composition of the material. As a result, the value of K21 will change continuously during a com­plete conversion of the ion-exchanger. Equations for the kinetics of such a conversion with variable K21 are given for a film diffusion controlled ion-exchange reaction.


RSC Advances ◽  
2016 ◽  
Vol 6 (105) ◽  
pp. 103215-103223 ◽  
Author(s):  
Yu-Qiao Zhang ◽  
Shun Li ◽  
Bo-Ping Zhang

A novel Bi2S3/CuS hybrid photocatalyst with a 3D hierarchical configuration was synthesized through an in situ solution-based cation exchange reaction that leads to obvious enhancements in charge separation and photocatalytic performance.


2012 ◽  
Vol 198-199 ◽  
pp. 85-88
Author(s):  
Shui Li Lai ◽  
Ying Hua Gao

In this paper,the organo-montmorillonite (OMMT) was prepared by cation exchange reaction, using sodium montmorillonite (Na+-MMT) and cetyltrimethylammonium bromide(CTAB) as all intercalation agent under precision microwave organic synthesis system. The structure of the montmorillonite was characterized by X-ray diffraction (XRD)、infrared spectrum (IR)、thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). The results show that the intercalation is successful, the CTAB as a organic modifier introuduced into lattice layers of montmorillonite by cation-exchange reaction and the surface morphology of OMMT is complete exfoliation, the distance between the lattice layers of montmorillonite has been greatly increased.


2019 ◽  
Vol 322 (3) ◽  
pp. 1771-1776
Author(s):  
D. Buzetzky ◽  
E. M. Kovács ◽  
M. N. Nagy ◽  
J. Kónya

Abstract Pertechnetate anion sorption was investigated on modified bentonites. Mn-, Cr-, Sn-bentonites were prepared by ion exchange process to sorb radioactive pertechnetate ions. In the case of Mn-, Cr-bentonite the sorb amount of metal ion was 70–90% of the cation exchange capacity of the bentonite which is expected. Interestingly in the case of Sn-bentonite this amount was 1.42 times higher than the cation exchange capacity. On Mn-bentonite the sorption was 35% at pH 5. The removal of pertechnetate ions was 100% on Cr-, Sn-bentonites and the significant sorption was achieved below 650 mV/SHE.


2015 ◽  
Vol 51 (45) ◽  
pp. 9381-9384 ◽  
Author(s):  
Peng Hu ◽  
Chee Keong Ngaw ◽  
Yee Yan Tay ◽  
Shaowen Cao ◽  
James Barber ◽  
...  

Single-crystalline-like p–n type CuInS2/NaInS2 heterogeneous nanosheets were synthesized by partial cation exchange reaction.


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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