scholarly journals Amidoxime-functionalized bead cellulose for the decomposition of highly toxic organophosphates

RSC Advances ◽  
2021 ◽  
Vol 11 (29) ◽  
pp. 17976-17984
Author(s):  
Pavel Janoš ◽  
Oldřich Tokar ◽  
Marek Došek ◽  
Karel Mazanec ◽  
Petr Ryšánek ◽  
...  
Keyword(s):  

Amidoxime-functionalized bead cellulose accelerates the cleavage of phosphoester bonds in toxic organophosphates.

1992 ◽  
Vol 57 (7) ◽  
pp. 1393-1404 ◽  
Author(s):  
Ladislav Svoboda ◽  
Jan Uhlíř ◽  
Zdeněk Uhlíř

The properties of Ostsorb DETA, a selective ion exchanger based on modified bead cellulose with chemically bonded diethylenetriamine functional groups, were studied, and its applicability to the preconcentration of trace amounts of lead from aqueous solutions was verified. The conditions of the preconcentration procedure in the column and batch modes were optimized for this purpose. The results obtained were applied to the determination of lead in phosphoric acid.


1993 ◽  
Vol 58 (2) ◽  
pp. 445-451 ◽  
Author(s):  
Vladimír Žúbor ◽  
Albert Breier ◽  
Marta Horváthová ◽  
Dagmar Hagarová ◽  
Peter Gemeiner ◽  
...  

The crude extract of cytosole enzymes was obtained from homogenized cells of Saccharomyces cerevisiae by partition. The enzyme was then isolated from the lower aqueous phase displaying higher glycerol kinase activity by dye-ligand chromatography on Cibacron Blue (CB) or Remazol Brilliant Blue R (RB)-derivatized bead-cellulose, ATP being the eluent. The specific activity of glycerol kinase rised more than 10 and 7-times after affinity dye-ligand chromatography and hydrophobic interaction chromatography, respectively. Glycerol kinase obtained by the latter method was purified by CB-bead cellulose. The final preparation maintained its enzymic activity without noticeable losses during a long-term storage at 4 °C in dark.


1989 ◽  
Vol 54 (9) ◽  
pp. 2375-2385 ◽  
Author(s):  
Peter Gemeiner ◽  
Eva Hrabárová ◽  
Magdaléna Zacharová ◽  
Albert Breier ◽  
Milan J. Beneš

Hydrophobization of bead cellulose is described, carried out by its alkylation with 1,2-epoxy-3-phenoxypropane under the conditions of acid (perchloric acid, borontrifluoride diethyl etherate) and basic (sodium hydroxide) catalysis. Reaction conditions (temperature, reaction time, molar ratio of reactants) have been determined, allowing the hydrophobization of bead cellulose to be carried out to the largest possible extent while maintaining its spherical shape. The nonstoichiometric mechanism suggested for the adsorption of amphiphilic adsorptives on bead 2-hydroxy-3-phenoxypropyl-cellulose (HPP-C) was checked by means of adsorption of six proteins. It was found that the surface of the hydrophobic segment of the adsorbent must be sufficiently large to be able to come in touch with the hydrophobic region of the protein through its multiple residues. In such cases the partitioning of the protein between the hydrophobic segment present as a liquid-like film and the surrounding solution becomes the predominant step of the adsorption. This adsorption mechanism is also reflected in zonal chromatography on bead HPP-C, as no displacement phenomena could be observed in any of the six proteins used. Retention of these proteins has been affected to a decisive extent by the degree of hydrophobization of HPP-C.


1983 ◽  
Vol 48 (1) ◽  
pp. 267-278 ◽  
Author(s):  
Peter Gemeiner ◽  
Milan Beneš

The acid catalyzed etherification of cellulose with 1-chloro-2,3-epoxypropane yielded 3-chloro-2-hydroxypropylcellulose (SCl ≤ 0.67); the latter, by a known sequence of reactions through the thiosulphate derivative and after its reduction, gave 2-hydroxy-3-mercaptopropylcellulose (up to 0.43 mmol SH/g). Mercaptodeoxycellulose (up to 0.53 mmol SH/g) was prepared from the less reactive chlorodeoxycellulose by an analogous sequence of reactions. Bead mercaptodeoxycellulose is more advantageous obtained by using tosylate of bead cellulose; this procedure is also more advantageous than the preparation of bead 2-hydroxy-3-mercaptopropylcellulose. Disulphide derivatives of cellulose were prepard (a) by a quantitative reaction of thiol derivatives with 2,2'-dipyridyl disulphide and (b) by a reversible crosslinking of cellulose or carboxymethylcellulose with bifunctional disulphides. Disulphide derivatives of cellulose prepared by procedure (b) give after reduction thiol derivatives (up to 0.185 mmol SH/g), and further by employing procedure (a) yield 2-pyridyl disulphide derivatives.


1996 ◽  
Vol 10 (5) ◽  
pp. 363-366
Author(s):  
E. Stratilová ◽  
D. Mislovičová ◽  
M. Dzúrová

1995 ◽  
Vol 750 (1 Enzyme Engine) ◽  
pp. 441-443 ◽  
Author(s):  
PETER DOČOLOMANSKÝ ◽  
PETER GEMEINER ◽  
DANICA MISLOVIČOVÁ ◽  
VLADIMÍR ŠTEFUCA ◽  
BENGT DANIELSSON

2007 ◽  
Vol 42 (6) ◽  
pp. 1231-1243 ◽  
Author(s):  
Eva Mištová ◽  
Helena Parschová ◽  
Zdeněk Matějka

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