The ion exchange equilibria of Na+/K+ in nonaqueous and mixed solvents on a strong acid cation exchanger

2002 ◽  
Vol 57 (11) ◽  
pp. 1943-1954 ◽  
Author(s):  
Antonio de Lucas ◽  
Jose L. Valverde ◽  
Maria C. Romero ◽  
Julian Gómez ◽  
Juan F. Rodrı́guez
2002 ◽  
Vol 41 (12) ◽  
pp. 3019-3027 ◽  
Author(s):  
Juan F. Rodríguez ◽  
Antonio de Lucas ◽  
Jose R. Leal ◽  
Jose L. Valverde

2009 ◽  
Vol 1240 ◽  
Author(s):  
Prabir K Patra ◽  
Sukalyan Sengupta

AbstractWe have synthesized a series of ion exchange functionalized fibers (IXF) from polystyrene (PS) and polyacrylonitrile (PAN). To obtain strong-acid cation exchange fibers, polystyrene was sulfonated using specific sulfonation protocols. Micron sized fibers (average diameter of 100m) were then produced from the functionalized polystyrene using a single-screw extruder equipped with a 30 hole spinneret with orifice diameter of 0.5 mm with a precise screw speed of 5 rpm, pump speed of 15 rpm, and with a feed rate of 2.4 cc/min. The extruder zone temperature was kept at 250 – 270 °C. Fiber was drawn at 120 degree with a draw ratio of 2. Electrospinning of functionalized polystyrene was also carried out to produce ultrafine functionalized fibers of 100 nm in average diameter. We have also electrospun polystyrene and polyisoprene blended nanofibers to increase the strength of the resulting blend nanofibers compared to pure PS nanofibers. To synthesize weak-acid cation exchange fibers polyacrylonitrile (PAN) was electrospun and the nanofibers obtained were alkaline hydrolyzed with 2 N NaOH for 20 minutes at room temperature to convert nitrile bonds to carboxylate. Cation exchange capacity (CEC) of the microfibers and nanofibers was determined. Sulfonated PS microfibers show high CEC of 4.0 meq/gm compared to that of nanofibers with 2.5 meq/gm. CEC of blended nanofibers of PS and polyisoprene was 2.0 meq/gm. In case of PAN fibers, nanosized electrospun fibers were found to show a CEC of 1.5 meq/gm. Weak-base anion exchange fiber synthesis was undertaken using appropriate protocol and its CEC was measured. For all IXF synthesized, fiber diameter was measured using SEM, degree of functionalization was qualitatively determined using FTIR and ion exchange capacity was computed after mass balance on a binary exchange system after equilibrium.


AIChE Journal ◽  
1989 ◽  
Vol 35 (1) ◽  
pp. 53-68 ◽  
Author(s):  
Malcolm S. Saunders ◽  
John B. Vierow ◽  
Giorgio Carta

2017 ◽  
Vol 92 (7) ◽  
pp. 1678-1689 ◽  
Author(s):  
Pengfei Jiao ◽  
Jinglan Wu ◽  
Yingying Wang ◽  
Jingwei Zhou ◽  
Wei Zhuang ◽  
...  

2016 ◽  
Vol 4 (2) ◽  
pp. 2216-2224 ◽  
Author(s):  
Nathan Pember ◽  
Graeme J. Millar ◽  
Sara J. Couperthwaite ◽  
Mitchell de Bruyn ◽  
Kenneth Nuttall

1969 ◽  
Vol 49 (3) ◽  
pp. 273-286
Author(s):  
B. A. Smith ◽  
F. Sánchez-Nieva ◽  
M. A. González ◽  
M. Matos-Maldonado

Investigations of the chemical requirements for regeneration of the first-anion and the cation-exchanger beds of the reverse-cycle system were undertaken in these studies, but no attempt was made to establish the requirements for the second-anion exchanger bed. A large dosage of NaOH to provide superior exchanger capacity was used for the highly basic anion resin in first position, and by recycling usable portions of the waste regenerant in a subsequent test, an average of 114 percent of the stoichiometric quantity of NaOH was consumed per test. No change in performance of the exchanger system was detected following adoption of such a regenerant recycling procedure. Efforts to obtain satisfactory regeneration of the weakly acid cation exchanger with H2SO4 were discouraging. The quantity of material which could be processed per test was less, the percentage removals of ash and protein were less, and the ash-percent-dry solids remaining in the product juices was 79-percent greater than when HCl was employed as regenerant. Juice purities following ion-exchange processing were found to have increased by approximately one-half as much with H2SO4  regeneration as with HC1. Examination of the product juices revealed that their potassiumion contents were much greater during H2SO4  regeneration tests than while HC1 was used. Apparently the large quantities of calcium and magnesium ions found in cane juices were not efficiently regenerated from the exchanger resin by H2SO4 , and that part which remained in the resin during subsequent juice deionization increased the leakage of potassium ions into the product juices. Although HC1 was much more expensive than H2SO4, the recycling of excess regenerant to reduce the quantity consumed to approximately 105 percent of the necessary stoichiometric requirement would make the use of this more costly acid economically attractive. Information was obtained in these tests which showed the importance of efficient backwashing of the highly basic first anion bed in order to eliminate significant quantities of Mg(OH)2, and organic materials precipitated on the resin particles during passage of juices through the bed. The effective backwashing obtained in the semipilot-plant column was not always attained in the smaller laboratory column and some insoluble materials remained following backwashing and regeneration.


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