scholarly journals The Li+, Na+ and K+ ion exchange reaction process on the surface of mixed oxide SiO2/TiO2/Sb2O5 surface prepared by the sol-gel processing method

2005 ◽  
Vol 30 (1) ◽  
pp. 51-58 ◽  
Author(s):  
C. U. Ferreira ◽  
J. E. Gonçalves ◽  
Y. V. Kholin ◽  
Y. Gushikem

The porous mixed oxide SiO2/TiO2/Sb2O5 obtained by the sol-gel processing method presented a good ion exchange property and a high exchange capacity towards the Li+, Na+ and K+ ions. In the H+/M+ ion exchange process, the H+ / Na+ could be described as presenting an ideal character. The ion exchange equilibria of Li+ and K+ were quantitatively described with the help of the model of fixed tetradentate centers. The results of simulation evidence that for the H+ / Li+ exchange the usual situation takes place: the affinity of the material to the Li+ ions is decreased with increasing the degree of ion exchange. On the contrary, for K+ the effects of positive cooperativity, that facilitate the H+ / K+ exchange, were revealed.

Author(s):  
Abdelhamid Addala ◽  
Moussa Boudiaf ◽  
Maria Elektorowicz ◽  
Embarek Bentouhami ◽  
Yacine Bengeurba

Abstract Under varied conditions, the IRC 718 ion-exchange resin is used to extract chromium (VI) ions from aqueous solutions. On chromium (VI) removal effectiveness, the effects of adsorption dosage, contact time, beginning metal concentration, and pH were examined. The batch ion exchange process reached equilibrium after around 90 minutes of interaction. With an initial chromium (VI) concentration of 0.5 mg/dm3, the pH-dependent ion-exchange mechanism revealed maximal removal in the pH 2.0–10 range . The adsorption mechanism occurs between Cr(VI) determined as the electron acceptor, and IRC 718 determined as the electron donor. The equilibrium ion-exchange potential and ion transfer quantities for Amberlite IRC 718 were calculated using the Langmuir adsorption isotherm model. The overall ion exchange capacity of the resin was determined to be 187.72 mg of chromium (VI)/g of resin at an ideal pH of 6.0.


Energies ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1800
Author(s):  
Sri Rahayu ◽  
Adi Ab Fatah ◽  
Girish M. Kale

The perovskite nanopowders of lanthanum strontium cobalt ferrite (LSCF) have been synthesized using the alginate mediated ion-exchange process. This perovskite-based material is a promising cathode for intermediate-temperature solid oxide fuel cells (IT-SOFCs) due to its high electrical conductivity, low polarizability, high catalytic activity for oxygen reduction, enhanced chemical stability at an elevated temperature in high oxygen potential environment and high compatibility with the ceria based solid electrolytes. Phase pure LSCF 6428, LSCF 6455, and LSCF 6482 corresponding to La0.6Sr0.4Co0.2Fe0.8O3-δ, La0.6Sr0.4Co0.5Fe0.5O3-δ, and La0.6Sr0.4Co0.8Fe0.2O3-δ, respectively were successfully synthesized. The simultaneous thermal analysis (DSC-TGA) and XRD were used to determine the optimum calcination temperature for the dried ion-exchanged beads. Single phase nanopowders of LSCF (6428, 6455, and 6482) have been successfully prepared at a calcination temperature of 700 °C. The TGA analysis showed that every ton of LSCF-ALG dried beads can potentially yield 360 kg of LSCF nanopowders suggesting a potential for scaling-up of the process of manufacturing nanopowders of LSCF.


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.


2002 ◽  
Vol 756 ◽  
Author(s):  
Seiichi Suda ◽  
Hiroyuki Ishii ◽  
Kiyoshi Kanamura

ABSTRACTLithium ionic conductor, (La, Li)TiO3, has synthesized with La/Li-TiO2 amorphous spheres that were obtained by sol-gel and ion-exchange method, and succeeding La3+/Li+ partial ion exchange. In this work, La /Li ion exchange conditions were mainly investigated in order to obtain dense (La, Li)TiO3 ceramics that have highly ionic conductivities. La +/Li+ ion exchange behavior was changed with ion-exchange solutions, and the Li/Ti ratio was increased with an increase in ethanol/water ratio in the solvent used for La3+/Li+ partial ion exchange. The use of an adequate ethanol/water ratio resulted in La/Li-TiO2 amorphous spheres with the composition of La/Li/Ti=0.54/0.34/1.00, and sintering of the spheres at 1200°C for 5 h in air led to dense (La, Li)TiO3 ceramics which exhibit the conductivity of 4.0 × 10-3 S cm-1 at 25°C.


2007 ◽  
Vol 32 (2) ◽  
pp. 41-45 ◽  
Author(s):  
J. E. Gonçalves ◽  
U.P. R. Filho ◽  
D.W. Franco ◽  
Y. Gushikem

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 2991
Author(s):  
Carmelo Lo Vecchio ◽  
Alessandra Carbone ◽  
Stefano Trocino ◽  
Irene Gatto ◽  
Assunta Patti ◽  
...  

Tandem photo-electro-chemical cells composed of an assembly of a solid electrolyte membrane and two low-cost photoelectrodes have been developed to generate green solar fuel from water-splitting. In this regard, an anion-exchange polymer–electrolyte membrane, able to separate H2 evolved at the photocathode from O2 at the photoanode, was investigated in terms of ionic conductivity, corrosion mitigation, and light transmission for a tandem photo-electro-chemical configuration. The designed anionic membranes, based on polysulfone polymer, contained positive fixed functionalities on the side chains of the polymeric network, particularly quaternary ammonium species counterbalanced by hydroxide anions. The membrane was first investigated in alkaline solution, KOH or NaOH at different concentrations, to optimize the ion-exchange process. Exchange in 1M KOH solution provided high conversion of the groups, a high ion-exchange capacity (IEC) value of 1.59 meq/g and a hydroxide conductivity of 25 mS/cm at 60 °C for anionic membrane. Another important characteristic, verified for hydroxide membrane, was its transparency above 600 nm, thus making it a good candidate for tandem cell applications in which the illuminated photoanode absorbs the highest-energy photons (< 600 nm), and photocathode absorbs the lowest-energy photons. Furthermore, hydrogen crossover tests showed a permeation of H2 through the membrane of less than 0.1%. Finally, low-cost tandem photo-electro-chemical cells, formed by titanium-doped hematite and ionomer at the photoanode and cupric oxide and ionomer at the photocathode, separated by a solid membrane in OH form, were assembled to optimize the influence of ionomer-loading dispersion. Maximum enthalpy (1.7%), throughput (2.9%), and Gibbs energy efficiencies (1.3%) were reached by using n-propanol/ethanol (1:1 wt.) as solvent for ionomer dispersion and with a 25 µL cm−2 ionomer loading for both the photoanode and the photocathode.


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.


Sign in / Sign up

Export Citation Format

Share Document