Complex formation of thiocyanate ions with iron(III) on the solid phase of fibrous ion exchangers

2017 ◽  
Vol 72 (5) ◽  
pp. 542-545
Author(s):  
O. P. Shvoeva ◽  
V. P. Dedkova ◽  
A. A. Grechnikov
Author(s):  
V. S. Soldatov ◽  
I. S. Elinson ◽  
A. A. Shunkevich ◽  
L. Pawlowski ◽  
H. Wasag

2020 ◽  
Vol 4 (3) ◽  

Inorganic sorbents, in comparison with ordinary organic ion exchangers, have higher selectivity, radiation, thermal, and chemical stability. Inorganic ion exchangers are universal materials exhibiting both cation exchange and anion exchange properties. In this work, using aluminum hydroxide (AHO) as an example, we study the possibility of expanding the range of metal oxyhydrates that can serve as the basis to produce inorganic anion-exchange materials. The properties of aluminum hydroxide largely depend on the method of its production. This phenomenon is associated with a different state of Al3+ ions in aqueous solutions during hydrolysis. Estimation of the size of the primary particles of hydrated alumina gives a value of 19 nm. The most potent effect on the structure and ion-exchange properties of aluminum hydroxide is exerted by the introduction of alloying elements into its composition. Isomorphic substitution of a part of Al(III) ions in the structure of aluminum hydroxide with ions with a higher charge (Ti(IV), Zr(IV), or W(VI)) leads to an increase in the content of exchangeable OH-groups in the resulting material. The synthesized materials are amorphous substances, to study their structure; the method of diffuse X-ray scattering was used. The Gibbsite structural motif is determined, and structural changes occurring under the influence of various factors, and synthesis conditions are analyzed. By optimizing the composition of the material, it is possible to improve its sorption characteristics significantly. AAW-0, AAZ-0, and AAT-0 anion exchangers synthesized based on hydrated aluminum oxide can be used to purify weakly acidic electrolyte solutions from anionic impurities in the dynamic mode of repeated sorptiondesorption cycles. Materials based on mixed hydrated oxides of various elements can also be used as catalyst supports. Their anion exchange properties allow a wide range to vary the number of different anions introduced into the solid phase and, accordingly, to regulate the number and state of active catalytic sites.


1980 ◽  
Vol 36 (6) ◽  
pp. T253-T259 ◽  
Author(s):  
Tokuhisa Miyamatsu ◽  
Noboru Oguchi

Author(s):  
Anatoly M. Dolgonosov ◽  
Ruslan Kh. Khamizov ◽  
Nadezhda K. Kolotilina

Nano-sized particles of functional polymers i.e. nano-ion-exchangers (NIEX), are unusual objects which simultaneously behave as the hyper-charged ions and the solid ion exchangers. Due to similar charges, they form very stable colloidal systems. This paper is devoted to theoretical and practical study of the proper- ties of nano-exchangers, methods for their preparation, the technique of experiments being practically un- known, and the opportunities for their application. The results of dynamic experiments are given for sorption of nano-exchangers and the ions of back- ground solutions on the beds of macro-particles of usual cationic and anionic resins. It is shown how to ob- tain the NIEX hydrosols with the desired ionic composition, and the concept of the standard state hydrosol is defined. The possibility for solid-phase exchange of counter ions between contacting particles of the same polarity is demonstrated. The possibilities and advantages of using nano-ion-exchangers in chemical analysis are demonstrat- ed by different examples: preparation of separating phases for ion chromatography, application as modifier in capillary electrophoresis and using in photo-luminescence. The prospects of nano-ion-exchangers for drug delivery are also shown.


JOM ◽  
2002 ◽  
Vol 54 (10) ◽  
pp. 47-51 ◽  
Author(s):  
R. M. Kautzmann ◽  
C. H. Sampaio ◽  
J. L. Cortina ◽  
V. Soldatov ◽  
A. Shunkevich

1971 ◽  
Vol 123 (5) ◽  
pp. 789-803 ◽  
Author(s):  
M. Nieto ◽  
H. R. Perkins

Vancomycin forms complexes with peptides terminating in d-alanyl-d-alanine that are analogous to the biosynthetic precursors of bacterial mucopeptides. The specificity of complex-formation has been studied by means of many synthetic peptides, prepared by both solid-phase and conventional methods. The following conclusions can be drawn: (a) three amide linkages are required to form a stable complex; (b) the terminal carboxyl group must be free; (c) the carboxyl terminal and subterminal residues must be either glycine or of the d-configuration; (d) the size of the side chain in these residues greatly influences the affinity for vancomycin, a methyl group being the optimum in each case; (e) the nature of the side chain in the third and fourth residues has a smaller effect on complex-formation, but an l-configuration was somewhat better than a d-configuration in the third position. In addition to acyl-d-alanyl-d-alanine, other peptides that occur in bacterial cell walls will combine with vancomycin, although less strongly, e.g. acyl-d-alanyl-d-α-amino acid (where the terminal d-residue may form the cross-link in mucopeptide structure) and acyl-l-alanyl-d-glutamylglycine (a sequence found in the mucopeptide of Micrococcus lysodeikticus and related organisms). These results throw some light on the specificity of the uptake of vancomycin by living bacteria.


1999 ◽  
Vol 17 (6) ◽  
pp. 1587-1602
Author(s):  
D. PETRUZZELLI ◽  
R. CICCIOMESSERE ◽  
N. LIMONI ◽  
R. PASSINO ◽  
V.S. SOLDATOV

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