scholarly journals Modified Phillipsite as a Novel Ion-Exchanger for Potassium Extraction from Seawater

2019 ◽  
Vol 25 (4) ◽  
pp. 441-445
Author(s):  
Chunxia MENG ◽  
Jin HOU
Keyword(s):  
Hydrothermal Synthesis ◽  
Ion Exchange ◽  
Average Particle Size ◽  
Selectivity Coefficient ◽  
Exchange Capacity ◽  
Ion Exchanger ◽  
Average Particle ◽  
Mixed Solution ◽  
Ion Exchange Capacity ◽  
X Ray

Template-free preparation of phillipsite as a novel K+ ion-exchanger was studied systematically by hydrothermal synthesis. The alkalinity, dosage of water glass, dosage of H2O, aging time, reaction temperature and time of hydrothermal synthesis were discussed in detail. The optimized material obtained about phillipsite through the synthesis and testing methods was performed. The K+ ion-exchange capacity and selectivity coefficient were tested. The molar composition for preparing high performance phillipsite obtained was 2K2O:18SiO2:Al2O3:510H2O by optimizing synthetic conditions. The K+ ion-exchange capacity of phillipsite was 57.3 mg/g in seawater. The K+ selectivity coefficient was 88.6 in an equimolar K+ and Na+ mixed solution. Phillipsite can selectively capture K+ over other ions, and therefore can be used for potassium extraction selectively from seawater. Phillipsite was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). The XRD pattern indicated that the synthetic zeolite was phillipsite. The phillipsite particles exhibited cross-like shape and the average particle size was about 2.5 μm. The synthetic phillipsite was mainly consisted of Si, Al, K and O elements.

The Synthesis and Ion-Exchange Property of Inorganic Material Mg1.5Mn0.5Ti0.75O4

2012 ◽  
Vol 511 ◽  
pp. 105-108
Author(s):  
Jin He Jiang
Keyword(s):  
Ion Exchange ◽  
Inorganic Material ◽  
Exchange Capacity ◽  
Exchange Property ◽  
Insertion Reaction ◽  
Ion Exchange Capacity ◽  
X Ray ◽  
Thermal Crystallization ◽  
Crystallization Method ◽  
Saturation Capacity

Mg1.5Mn0.5Ti0.75O4 was prepared by a coprecipitation/thermal crystallization method. The extraction/insertion reaction with this material was investigation by X-ray, saturation capacity of exchange, and Kd measurement. The acid treatments of Mg1.5Mn0.5Ti0.75O4 caused Mg2+ extractions of more than 72%, while the dissolutions of Mn4+ and Ti4+ were less than 8.2%. The results showed that the Li+ extraction/insertion be progressed mainly by an ion-exchange mechanism. The acid treated samples had an ion exchange capacity of 10.6mmol/g for Li+.

Ion exchange of H+/Na+ in polyantimonic acid, doped with vanadium ions

2020 ◽  
Vol 92 (3) ◽  
pp. 505-514
Author(s):  
Liliya Yu. Kovalenko ◽  
Vladimir A. Burmistrov ◽  
Yuliya A. Lupitskaya ◽  
Fedor A. Yaroshenko ◽  
Elena M. Filonenko ◽  
...  
Keyword(s):  
Ion Exchange ◽  
Exchange Capacity ◽  
Unit Cell ◽  
Ion Exchange Capacity ◽  
Solid Solution Formation ◽  
X Ray ◽  
Polyantimonic Acid ◽  
Section Size ◽  
Pyrochlore Type ◽  
Vanadium Ions

AbstractThe influence of doping of polyantimonic acid with vanadium ions on the ion exchange H+/Na+ kinetics is determined. With the help of the X-ray analysis it is shown that doped compounds H2Sb2-xVxO6-δ  · nH2O, where x = 0.14; 0.36; 0.48 have the pyrochlore-type structure. With the increase of the amount of vanadium in a sample there is a decrease of a unit cell parameter. It is determined that there is a reduction of a unit cell frame, formed by antimonic and vanadium ions, and a size reduction of hexagonal cavities, in which protons are located. It is shown that during the ion exchange of H+/Na+ there is a change of the unit cell plane without a symmetry breaking of a crystal structure, which demonstrates solid solution formation. With the increase of the amount of vanadium in the sample there is a decrease of the ion-exchange capacity, which is connected with the decrease of the channel’s section size. The ion exchange H+/Na+ kinetics has been studied with the approximation of the Boyd’s model for the intergrain diffusion. Diffusion coefficients had the order 10−13 m2/s and decreased with the increase of the amount of vanadium in the sample.

The Synthesis and Ion-Exchange Property of Li+ Memorized Inverse Spinel Mg2Ti0.5(PO4)2

2012 ◽  
Vol 512-515 ◽  
pp. 1014-1017
Author(s):  
Jin He Jiang
Keyword(s):  
Ion Exchange ◽  
Exchange Capacity ◽  
Exchange Property ◽  
Inverse Spinel ◽  
Spinel Type ◽  
Ion Exchange Capacity ◽  
X Ray ◽  
Crystallization Method ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

A inverse spinel-type metal compound [Mg2Ti0.5(PO4)2], was prepared by a solid state reaction crystallization method. The Li+extraction/insertion with this material were investigated by X-ray, FT-IR spectroscopy, and Kd measurement, The acid treated samples had an ion exchange capacity of 8.7mmol/g for Li+. It had a memorial ion-sieve property for Li+.

Property of LiMn0.5Ti0.75O3 Type Ion-Exchangers and Extraction for Lithium

2012 ◽  
Vol 549 ◽  
pp. 118-121
Author(s):  
Jin He Jiang
Keyword(s):  
Solid State ◽  
Ion Exchange ◽  
Solid State Reaction ◽  
Exchange Capacity ◽  
Exchange Mechanism ◽  
Metal Compound ◽  
Spinel Type ◽  
Ion Exchange Capacity ◽  
X Ray ◽  
Crystallization Method

A spinel-type metal compound [LiMn0.5Ti0.75O3], was prepared by a solid state reaction crystallization method. The Li+ extraction/insertion with this material were investigated by X-ray and Kd measurement. The results showed that the Li+ extraction/insertion be progressed mainly by an ion-exchange mechanism. The acid treated samples had an ion exchange capacity of 4.2mmol/g for Li+.

scholarly journals ADSORPTION OF Ca(II), Pb(II) AND Ag(I) ON SULFONATO-SILICA HYBRID PREPARED FROM RICE HULL ASH

2011 ◽  
Vol 11 (3) ◽  
pp. 273-278 ◽  
Author(s):  
Siti Sulastri ◽  
Nuryono Nuryono ◽  
Indriana Kartini ◽  
Eko Sri Kunarti
Keyword(s):  
Aqueous Solution ◽  
Ion Exchange ◽  
Functional Group ◽  
Sodium Hydroxide Solution ◽  
Exchange Capacity ◽  
Rice Hull ◽  
Rice Hull Ash ◽  
Ion Exchange Capacity ◽  
X Ray ◽  
Silica Hybrid

In this research, adsorption of Ca(II), Pb(II) and Ag(I) in aqueous solution onto sulfonato-silica hybrid (SSH) prepared from rice hull ash (RHA) has been studied. The preparation of SSH adsorbent was carried out by oxidation of mercapto-silica hybrid (MSH) with hydrogen peroxide (H2O2) solution 33%. MSH was prepared, via sol-gel process, by adding 3 M hydrochloric acid solution to mixture of sodium silicate (Na2SiO3) solution and 3(trimethoxysilyl)-1-propanthiol (MPTS) to reach pH of 7.0. Solution of Na2SiO3 was generated from destruction of RHA with sodium hydroxide solution followed with heating at 500 °C for 30 min. The SSH produced was characterized with Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) analyzer, energy dispersive X-ray (EDX) spectroscopy and determination of ion-exchange capacity for sodium ion (Na+). The adsorption of Ag(I) and Ca(II) were conducted in a batch system in various concentrations for one hour. The adsorbent ion was calculated based on difference of concentrations before and after adsorption process determined using atomic absorbance spectrophotometric (AAS) method. The adsorption character was evaluated using model of isotherm Langmuir and Freundlich adsorption to calculate the capacity, constants and energy of adsorption. Result of characterization by EDX and FTIR showed qualitatively that SSH has been successfully synthesized which were indicated by appearance of characteristic absorbance of functional group namely silanol (Si-OH), siloxane (Si-O-Si), methylene (-CH2-) and disappearance of mercapto group (SH). The XRD data showed amorphous structure of SSH, similar to silica gel (SG) and MSH. The study of adsorption thermodynamics showed that oxidation of MSH into SSH increases the ion-exchange capacity for Na+ from 0.123 to 0.575 mmol/g. The change in functional group from silanol to mercapto and from mercapto to sulfonato increases the adsorption capacity of Ca(II). However, the capacity order of adsorbents for both ions of Pb(II) and Ag(I) in aqueous solution is MSH > SG > SSH.

scholarly journals Synthesis of rare-earth nanosized phosphors using microwave processing

2021 ◽  
Vol 2056 (1) ◽  
pp. 012049
Author(s):  
A B Vlasenko ◽  
V V Bakhmetyev
Keyword(s):  
Particle Size ◽  
Hydrothermal Synthesis ◽  
Visible Light ◽  
Average Particle Size ◽  
Microwave Treatment ◽  
Viral Diseases ◽  
Medical Applications ◽  
Average Particle ◽  
Light Spectrum ◽  
X Ray

Abstract Nanomaterials find permanently extending applications in various areas of life. In particular, nanosized phosphors can be used as pharmaceutical carriers capable of emitting ultraviolet or visible light that activates a photosensitizer, thus significantly expanding the possibilities of photodynamic therapy in the treatment of oncological, bacterial and viral diseases. The conditions required for the use of nanosized phosphors in medicine include their fine dispersion and effective luminescence in the red region of visible light spectrum upon stimulation by X-ray radiation of the range accepted for medical applications, particularly for diagnostic and therapeutic purposes in many diseases. The aim of this work was to study the effect of microwave treatment of Y2O3:Eu phosphors prepared by hydrothermal synthesis in ethylene glycol at 230 °C for 6 hours, involving the decomposition of mixed acetate. In order to reduce the aggregation and growth of the resulting particles, Aerosil A300 with average particle size 7 nm was added to the reaction mixture in the course of hydrothermal synthesis in the ratio 1:1 relating to the obtained phosphor. The microwave treatment was carried out at 800 °C for 5 minutes. The developed method provided Y2O3:Eu phosphor samples featuring with increased luminescence intensity in the region 610…700 nm compared to similar phosphors earlier prepared using the rapid thermal annealing (RTA) procedure.

DETERMINATION OF CHROMIUM(VI) IN WATER BY PIXE ANALYSIS USING ION EXCHANGE PAPER — LIMIT OF DETECTION AND INTERFERENCE BY COEXISTING ANIONS

2009 ◽  
Vol 19 (01n02) ◽  
pp. 1-8 ◽  
Author(s):  
SUREERAT THOMYASIRIGUL ◽  
HITOSHI FUKUDA ◽  
JUN HASEGAWA ◽  
YOSHIYUKI OGURI
Keyword(s):  
Ion Exchange ◽  
Proton Energy ◽  
Limit Of Detection ◽  
Deae Cellulose ◽  
Exchange Capacity ◽  
Ion Exchange Capacity ◽  
Pixe Analysis ◽  
X Ray ◽  
Chromium Vi

Concerning the PIXE analysis of Cr ( VI ) in water using ion-exchange filters, the limit of detection (LOD) and the influence of matrix anions were investigated. In order to look for the experimental condition for obtaining the minimum LOD, we measured the Cr - K α X-ray counts and background counts under the K α X-ray peak as a function of the incident proton energy and the thickness of the Mylar absorber foil in front of the detector. To investigate the interference by coexisting anions, each of PO 43-, SO 42-, NO 3-, Cl -, and F - ions and Cr ( VI ) ions were mixed in aqueous solutions and adsorbed on DE81-DEAE cellulose paper, a weakly basic anion exchanger with diethylaminoethyl functional groups. Then the filter samples were measured by PIXE using 2.5 MeV proton beams. We obtained a LOD of 0.16 µg or 8 ppb for 20 mL samples at a proton energy of 2.5 MeV and a Mylar film thickness of 50 or 100 µm. The experimental results on the mixed solutions indicated that NO 3-, Cl -, and F - as coexisting ions didn't interfere significantly with determination of a 50 µ g / L Cr ( VI ) concentration for 40 mL total solution volume, despite the total amount of anions was about 90% of ion exchange capacity of a filter. On the other hand, slight interferences by PO 43- ions were observed. However, under the same condition, we found that if the total amount of SO 42- ions was higher than 20% of ion exchange capacity, they induced significant interferences in determining Cr ( VI ).

The Synthesis and Ion-Exchange Property of Li+ Memorized Inverse Spinel Al0.75Fe1.25(PO4)2

2012 ◽  
Vol 490-495 ◽  
pp. 3864-3867
Author(s):  
Jin He Jiang ◽  
Bin Shan
Keyword(s):  
Ion Exchange ◽  
Exchange Capacity ◽  
Exchange Property ◽  
Inverse Spinel ◽  
Spinel Type ◽  
Ion Exchange Capacity ◽  
X Ray ◽  
Crystallization Method ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Compound Al0.75Fe1.25(PO4)2, a inverse spinel-type metal compound, was prepared by a solid state reaction crystallization method. The Li+ extraction/insertion with this material were investigated by X-ray, FT-IR spectroscopy, and Kd measurement, The chemical analysis showed that the Li+ extraction/insertion be progressed mainly by an ion-exchange mechanism. The acid treated samples had an ion exchange capacity of 4.0mmol/g for Li+. It had a memorial ion-sieve property for Li+.

Preparation of Cation Exchanger Using Electrospun Polystyrene Nanofiber

2006 ◽  
Vol 10 (2) ◽  
pp. 196-200 ◽  
Author(s):  
Hyung-Hwan An ◽  
◽  
Changyun Shin ◽  
Keyword(s):  
Ion Exchange ◽  
Glass Fiber ◽  
Water Uptake ◽  
Cation Exchanger ◽  
Fiber Surface ◽  
High Water ◽  
Exchange Capacity ◽  
Experimental Results ◽  
Ion Exchanger ◽  
Ion Exchange Capacity

We studied a new ion exchanger for high ion exchange capacity (IEC) and rapid ion exchange. Polystyrene nanofiber ion exchangers (PSNIEs) were prepared by electrospinning from solutions of dissolved polystyrene followed by sulfonation. Coating and sulfonation were used to modify the glass fiber surface with polystyrene to produce cation exchanger fiber (CEF). We present new experimental results on the performance of PSNIE and CEF related to parameters of IEC, water uptake, and surface morpoholgy. IEC and water uptake of PSNIE depend on sulfonation time. IEC reached 3.74 mmol/g at relatively high water uptake of 0.6 to 0.77g H2O/g-dry-PNIE. IEC and water uptake of CEF reached 3.61mmol/g-CEF and 0.25g H2O/g-dry-CEF.

Synthesis and characterization of a new crystalline tin(IV) arsenophosphate ion exchanger

1990 ◽  
Vol 68 (2) ◽  
pp. 346-349 ◽  
Author(s):  
K. V. Surendra Nath ◽  
S. N. Tandon
Keyword(s):  
Ion Exchange ◽  
Cation Exchanger ◽  
Exchange Capacity ◽  
Ion Exchanger ◽  
Amorphous Precursor ◽  
X Ray ◽  
Inorganic Ion Exchanger ◽  
Inorganic Ion ◽  
Exchange Behaviour

A new crystalline layered inorganic ion exchanger tin(IV) arsenophosphate with the formula Sn(HAsO4)(HPO4)•H2O has been prepared by refluxing the amorphous precursor. This exchanger has been characterized by X-ray powder pattern, chemical analysis, IR spectra, and thermal dehydration. Its ion exchange behaviour towards sodium ions is reported. The exchanger has an exchange capacity of 5.36 mequiv./g for Na+. The performance of tin(IV) arsenophosphate is compared with crystalline tin(IV) phosphate and arsenate. Keywords: cation exchanger, crystalline tin(IV) arsenophosphate, ion exchange, thermal behaviour, X-ray studies.

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