scholarly journals Polyvinyl Alcohol-Montmorillonite composites for water purification: Analysis of clay mineral cation exchange and composite particle synthesis

Polyhedron ◽  
2021 ◽  
pp. 115297
Author(s):  
Karlena Brown ◽  
Mary Mendoza ◽  
Tamanika Tinsley ◽  
Madeleine Y. Bee-DiGregorio ◽  
Michael Bible ◽  
...  
2021 ◽  
Vol 17 ◽  
Author(s):  
Amita Somya ◽  
Mamata Singh

Background: With increasing population and decreased quality of drinking water, there is a great demand for the development of new materials and methods that can find applications in the purification of water. This paper presents our small effort from pollution to solution by presenting the synthesis method of new sodium lauryl sulphate supported thorium(IV) phosphate, its characterization, and disquisition of analytical applications by executing some dual separations of calcium. Methods: Sodium lauryl sulphate thorium(IV) phosphate was synthesized by sol gel method. The synthesized exchanger was characterized by some physico-chemical studies like powdered X-ray diffraction, Scanning electron microscopy, Thermo gravimetric-differential thermal analysis, EDAX and Fourier transform-infrared study and was also checked for its competency towards the ion exchange processes and in analytical chemistry. Results: The prominent characteristic of Sodium lauryl sulphate supported Thorium(IV) phosphate has been its tremendously high ion exchange capacity for sodium ions (3.10 meq/g) which is almost two and half times more than the exchange capacity of Thorium(IV) phosphate (ThP), i.e., 1.3 meq/g. The material was resulted in fibrous sheet which is quite thermally, mechanically stable and poorly crystalline. The material has shown selectivity towards Ca2+ and Hg2+ ions. Conclusion: The synthesized cation exchange material has been found quite thermally stable, showing drastically high exchange capacity and selectivity towards Hg2+ and Ca2+ metal ions which might be because of the use of an anionic surfactant, sodium lauryl sulphate while synthesis of Th(IV) phosphate which has played a key role in enhancing the exchange capacity and adsorption of specific metals as well. Therefore, based on the results obtained, the above said materials can find applications in water purification processes and also, in environmental pollution control where removal of Hg2+ and Ca2+ is required.


Molecules ◽  
2019 ◽  
Vol 24 (16) ◽  
pp. 3015
Author(s):  
Fethi Kooli ◽  
Souad Rakass ◽  
Yan Liu ◽  
Mostafa Abboudi ◽  
Hicham Oudghiri Hassani ◽  
...  

The effect of the counteranion of hexadecyltrimethylammonium salts on the physico-chemical properties of organoclays was investigated, using a selected natural clay mineral with a cation exchange capacity of 95 meq/100 g. The uptake amount of C16 cations was dependent on the hexadecyltrimethylammonium (C16) salt solution used, the organoclay prepared from C16Br salt solution exhibited a value of 1. 05 mmole/g higher than those prepared from C16Cl and C16OH salt solutions. The basal spacing of these organoclays was in the range of 1.81 nm to 2.10 nm, indicating a similar orientation of the intercalated surfactants, and could indicated that the excess amount of surfactants, above the cation exchange capacity of 0.95 meq/g could be adsorbed on the external surface of the clay mineral sheets. These organoclays were found to be stable in neutral, acidic, and basic media. The thermal stability of these organoclays was carried out using thermogravimetric analysis and in-situ X-ray diffraction (XRD) techniques. The decomposition of the surfactant occurred at a maximum temperature of 240 °C, accompanied with a decrease of the basal spacing value close to 1.42 nm. The application of these organoclays was investigated to remove an acidic dye, eosin. The removal amount was related to the initial used concentrations, the amount of the surfactants contents, and to the preheated temperatures of the organoclays. The removal was found to be endothermic process with a maximum amount of 55 mg of eosin/g of organoclay. The value decreased to 25 mg/g, when the intercalated surfactants were decomposed. The reuse of these organoclays was limited to four regeneration recycles with a reduction of 20 to 30%. However, noticeable reduction between 35% to 50% of the initial efficiency, was achieved after the fifth cycle, depending of the used organoclays.


Clay Minerals ◽  
1966 ◽  
Vol 6 (4) ◽  
pp. 341-344 ◽  
Author(s):  
W. E. Worrall ◽  
A. E. Cooper

AbstractA white-burning, highly-plastic clay from Jamaica, containing mainly disordered kaolinite, was examined recently. It was unusual in that it was practically free from fine mica, and therefore could be purified readily by standard sedimentation techniques.The cation exchange capacity was abnormally high, and the purified clay mineral, on analysis and calculation of the ionic composition, was found to be deficient in aluminium, but contained magnesium and iron.The results confirmed the view, previously expressed, that disorder in kaolinites is associated with a high cation exchange capacity and a substituted lattice.


1980 ◽  
Vol 43 (331) ◽  
pp. 865-872 ◽  
Author(s):  
D. C. Bain ◽  
P. F. S. Ritchie ◽  
D. R. Clark ◽  
D. M. L. Duthie

SummaryThe chemical, mineralogical, and textural changes involved in the weathering of basalt have been traced through various stages from fresh rock (which has a cation exchange capacity of 10 meq/100 g due to the presence of a swelling chlorite mineral) to reddened basaltic rubble consisting of interstratified montmorillonite-illite, hematite, and anatase. The cation exchange capacities of the rocks increase progressively with the formation of secondary clay from labradorite as Al, Fe, and Ti accumulate and Si, Mg, Ca, and Na are depleted—much of the K is retained in the secondary clay mineral. The weathering is considered to be contemporaneous with the formation of the Antrim bauxites but not so intense.


1987 ◽  
Vol 78 (1) ◽  
pp. 62-68 ◽  
Author(s):  
Masami Matsuda ◽  
Kiyomi Funabashi ◽  
Fumio Kawamura ◽  
Shunsuke Uchida ◽  
Katsumi Ohsumi

2020 ◽  
Vol 81 (3) ◽  
pp. 491-498
Author(s):  
Ling Chen ◽  
Shudi Mao ◽  
Zhe Li ◽  
Ying Yang ◽  
Ran Zhao

Abstract Constructing new cation exchange membranes (CEM) has been regarded as an easy and effective approach to improving the capacitive deionization (CDI) system. In this study, a new method of fabrication of CEM was introduced by crosslinking sulfosuccinic acid (SSA) and citric acid (CA). The SSA and CA were crosslinked with polyvinyl alcohol (PVA) to fabricate CEMs in a series of conditions. The ion transference number for each fabricated membrane was tested to select the optimal recipe. The membrane fabricated by the selected method was then tested in the CDI system and the results show that the total percentage of SSA could be reduced from 5% to 1% by adding 5 g of non-toxic and inexpensive CA. The cost of preparing the membrane also decreased from US$0.18 per square meter to US$0.03. The adsorption capacity and the charge efficiency of membrane capacitive deionization system (MCDI) coated with a PVA/SSA/CA layer (mass ratio 10:1:5) was compared with the normal CDI and the MCDI coated with the original membrane (PVA:SSA = 19:5), which is named O-MCDI). The results show that with the modified membrane, the adsorption capacity and the charge efficiency can be enhanced by 18% and 28% compared with the CDI. In addition, although the cost is reduced, the desalination efficiency is still guaranteed. The adsorption capacity and charge efficiency are still increased by about 3% compared with the O-MCDI.


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