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PubMed2003

Kinetics of removal of chromium from water and electronic process wastewater by ion exchange resins: 1200H, 1500H and IRN97H.

The removal of chromium from aqueous solution by an ion exchange resin is described. Ion exchange resins 1200H, 1500H and IRN97H show a remarkable increase in sorption capacity for chromium, compared to other adsorbents. The adsorption process, which is pH dependent show maximum removal of chromium in the pH range 2-6 for an initial chromium concentration of 10mg/l. The metal ion adsorption obeyed linear, Langmuir and Freundlich isotherms. The adsorption of chromium on these cation exchange resins follows first-order reversible kinetics and pseudo-first-order kinetics. The intraparticle diffusion of chromium on ion exchange resins represents the rate-limiting step. The uptake of chromium by the ion exchange resins was reversible and thus have good potential for the removal/recovery of chromium from aqueous solutions. We conclude that such ion exchange resins can be used for the efficient removal of chromium from water and wastewater.

Adsorption↗
PubMed1988

Quantitative analysis of resting membrane electrogenesis in insect (diptera) skeletal muscle. I. Intracellular K+, Na+ and Cl- activities, measured using liquid ion-exchanger and neutral ion-carrier microelectrodes.

Electrophysiological properties of skeletal body-wall muscles of prepupal Calliphora erythrocephala were investigated using double-barrelled intracellular ion-sensitive microelectrodes. The most realistic estimate of the intracellular K+ activity, obtained using K+-sensitive microelectrodes based on a neutral carrier, was 115 mmoll-1. The K+ equilibrium potential was consistently more negative than the prevailing resting potential, the average difference being -15 mV. The intracellular Na+ activity and the Na+ equilibrium potential were 7 mmoll-1 and +46 mV on average, respectively. The mean value of the intracellular Cl- activity was 40 mmoll-1, and this was apparently higher than that required for passive distribution of Cl-. However, when reversibly exposed to a Ringer containing no Cl-, cells could rapidly exchange most of their intracellular Cl-, although the resting membrane potentials were only transiently affected. It is concluded that an anionic interferent exists inside muscles, that this artefactually elevates the measured intracellular Cl- activities, and that Cl- makes no contribution to resting membrane electrogenesis.

Animals↗
PubMed2004

Comparison of the ion exchange uptake of ammonium ion onto New Zealand clinoptilolite and mordenite.

In this study the uptake performances of the naturally occurring zeolite, clinoptilolite, and of New Zealand mordenite are compared. The uptake of fully ionised ammonium ion from aqueous solutions in the concentration range 0-200 mg/l on to these two materials was compared. The influence of other cations present in water upon the ammonia uptake was also determined. The cations studied were potassium, calcium and magnesium. In all cases the anionic counterion present was chloride. The results showed that the mordenite exhibited higher overall uptake concentrations at equilibrium compared with clinoptilolite at solution concentrations greater than 80 mg/l. Beyond this value, the difference in solid-phase equilibrium concentrations on the mordenite became greater at higher solution-phase ammonium ion concentrations. The effect of the other cations upon uptake of ammonium ion was relatively small. In all cases, the ammonium ion showed the highest uptake on to both the mordenite and the clinoptilolite. In the case of clinoptilolite this was rather an unexpected result since the majority of other work shows clinoptilolite exhibiting a higher affinity for potassium ion compared with ammonium ion. This may be explained by the fact that the clinoptilolite came from volcanic deposits in New Zealand. This is the first such study on this material. At solution-phase equilibrium concentrations of greater than 80 mg/l, the mordenite showed smaller reductions in ammonium ion uptake in the presence of the other cations when compared with clinoptilolite.

Aluminum Silicates↗
PubMed2002

Clotrimazole-triiodide ion association as an ion exchanger for a triiodide ion-selective electrode.

A novel triiodide ion-selective electrode based on a clotrimazole-triiodide ion pair as a membrane carrier was prepared. It has a linear response to triiodide from 8 x 10(-6) to 5 x 10(-3) M with a slope of -68.9 mV per decade and a detection limit of 5 x 10(-6) M. The electrode response is independent of the pH of the solution in the pH range 2-9. It has a very short response time and can be used for at least 3 months without any considerable divergence in the potentials. The proposed sensor revealed very good selectivities for I3- over a variety of other anions. It was used as an indicator electrode in the potentiometric titration of triiodide ions and in an indirect potentiometric determination of clotrimazole in pharmaceutical preparations.

Clotrimazole↗
PubMed1996

Rapid purification and monitoring of immunoglobulin M from ascites by perfusion ion-exchange chromatography.

A purification and on-line monitoring procedure for IgM was developed. Perfusion ion-exchange chromatography was used for rapid purification of IgM from ascites fluid and hybridoma supernatant. Crude ascites was directly loaded onto an ion exchanger. Due to the complexity of IgM, a two-step ion-exchange procedure had to be developed. This procedure involved a rapid cation-exchange chromatography capture step followed by further purification using anion-exchange chromatography. High linear velocities, in excess of 3500 cm/h, enabled separations to be performed under 5 min. Purity of the final product by SDS-PAGE was shown to be greater than 95%. Furthermore, the antibodies retained biological activity as measured by indirect immunofluorescence (IIF) and ELISA. The IgM peak was also monitored on-line using a novel peak tracking approach. This involved placing an antibody column (specific to the IgM) prior to the ion-exchange column and operating the ion-exchange column with and without the antibody column in-line. The missing peak that is identified by comparing the two chromatograms indicates where the IgM elutes.

Animals↗
PubMed2002

Catalytic asymmetric dihydroxylation of olefins with reusable OsO(4)(2-) on ion-exchangers: the scope and reactivity using various cooxidants.

Exchanger-OsO(4) catalysts are prepared by an ion-exchange technique using layered double hydroxides and quaternary ammonium salts covalently bound to resin and silica as ion-exchangers. The ion-exchangers with different characteristics and opposite ion selectivities are specially chosen to produce the best heterogeneous catalyst that can operate using the various cooxidants in the asymmetric dihydroxylation reaction. LDH-OsO(4) catalysts composed of different compositions are evaluated for the asymmetric dihydroxylation of trans-stilbene. Resin-OsO(4) and SiO(2)-OsO(4) designed to overcome the problems associated with LDH-OsO(4) indeed show consistent activity and enantioselectivity in asymmetric dihydroxylation of olefins using K(3)Fe(CN)(6) and molecular oxygen as cooxidants. Compared to the Kobayashi heterogeneous systems, resin-OsO(4) is a very efficient catalyst for the dihydroxylation of a wide variety of aromatic, aliphatic, acyclic, cyclic, mono-, di-, and trisubstituted olefins to afford chiral vicinal diols with high yields and enantioselectivities irrespective of the cooxidant used. Resin-OsO(4) is recovered quantitatively by a simple filtration and reused for a number of cycles with consistent activity. The high binding ability of the heterogeneous osmium catalyst enables the use of an equimolar ratio of ligand to osmium to give excellent enantioselectives in asymmetric dihydroxylation in contrast to the homogeneous osmium system in which excess molar quantities of the expensive chiral ligand to osmium are invariably used. The complexation of the chiral ligand (DHQD)(2)PHAL, having very large dimension, a prerequisite to obtain higher ee, is possible only with the OsO(4)(2-) located on the surface of the supports.

Alkenes↗
PubMed2000

Coupling of chromatographic ion-exchange reaction with change-partner reaction. Presumed mechanism on the ion-ion interaction of inorganic ions in Sephadex G-15 columns.

A sample solution containing sodium or potassium dihydrogenphosphate or disodium or dipotassium hydrogenphosphate was eluted from a Sephadex G-15 column with either sodium or potassium chloride solution in various sample-eluent systems, and every one of the four kinds of ions employed was determined in the eluate. Then, the elution profiles showed the phenomenon that a negative peak of chloride ion coexisted in the fractions of a positive peak of phosphate ion, in all sample-eluent systems employed. This phenomenon was assumed to occur by the coupled reaction of change-partner and ion-exchange reactions including ion exclusion.

Chromatography, Ion Exchange↗
PubMed1992

Strengthening of feldspathic porcelain by ion exchange and tempering.

This study investigated the effectiveness of tempering and ion-exchange treatments on crack growth and bi-axial flexural strength of seven feldspathic porcelains. The results showed that tempering treatment was more effective in strengthening porcelain than was the ion-exchange process as measured by the bi-axial flexural strength. However, the results of initial crack size induced by a microhardness tester showed that ion-exchange yielded a surface that was more resistant to crack initiation than was that yielded by the tempering treatment. EDX and microprobe analyses showed that there was evidence of exchange between Na+ within the porcelain surface and K+ from the ion-exchange agent applied on the surface.

Aluminum Silicates↗
PubMed2006

Comparison of isotherms for the ion exchange of Pb(II) from aqueous solution onto homoionic clinoptilolite.

The ion exchange equilibrium of Pb(II) on clinoptilolite modified with NH(4)Cl and NaCl can be represented by two types of isotherms. The first one is the ion exchange isotherm based upon the constant of thermodynamic equilibrium for the ion exchange reaction; however, the fitting procedure for this isotherm can be very tedious due to all the calculations involved and additional thermodynamic data. The second one is the Langmuir isotherm. The use of the Langmuir isotherm to represent ion exchange equilibrium has increased in recent last years since it adequately fits the equilibrium data and, furthermore, its calculation is much simpler. A comparison between the two isotherms showed that they fitted the experimental data reasonably well, but the Langmuir isotherm is much simpler and easier to use.

Journal Article↗
PubMed2005

Separation of (134)Cs and (152)Eu using inorganic ion exchangers, zirconium vanadate and ceric vanadate.

Two inorganic ion exchangers, zirconium vanadate and ceric vanadate were synthesized and applied to confine and separate (152)Eu and (134)Cs from a synthetic mixture. The percentages of adsorption of the two radionuclides were studied for the two ion exchangers at varying pH conditions. At pH 3, zirconium vanadate adsorbs both Eu and Cs and a column chromatographic separation was achieved using 0.1M EDTA as the eluant. The ceric vanadate ion exchanger showed an increased trend in adsorption for both the radionuclides with increase of pH value from 1 to 6. At pH 1, a column chromatographic separation of these radionuclides from a mixture was achieved, because at this pH only (134)Cs was adsorbed to ceric vanadate bed in the column.

Journal Article↗
PubMed1985

Separation of hemoglobin variants by ion-exchange chromatography on Monobead resins.

Our studies on the separation of hemoglobin variants using Monobead ion exchangers show that these ion exchangers will resolve variants that heretofore could not be resolved. Procedures with these ion exchangers, therefore, extend our ability to detect hemoglobinopathies. Since it is also important to study the physicochemical properties of variants, their isolation is of critical importance to the researcher. The methods described in this report enable variants to be isolated in quantitative amounts so that such studies can be performed. Most isolations can be accomplished within 1 h, under mild conditions with aqueous buffers. Elution gradients can be changed conveniently to optimize resolution of most variants. These methods should serve as a valuable adjunct in studying the structure-function relationship of hemoglobin and other proteins.

Chromatography, Ion Exchange↗
PubMed1998

Preliminary report on fractionation of fucans by ion-exchange displacement centrifugal partition chromatography.

A new method combining ion-exchange displacement chromatography with centrifugal partition chromatography (CPC) was used for the fractionation of partially depolymerized fucans (polysulphated polysaccharides). The ion-exchanger was Amberlite LA2, a high-molecular-mass liquid secondary amine miscible with most common organic solvents and immiscible with aqueous solutions. Ion-exchange displacement centrifugal partition chromatography was performed with LA2 in methyl isobutyl ketone (MiBK) as the stationary phase, water as the mobile phase, Cl- as the carrier and OH- as the displacer. A complex mixture of partially depolymerized fucans was resolved into adjacent families characterized by their peak molecular mass and polydispersity. The Dubois test (sugar) and the azur A test (SO3-) confirmed the displacement mode of the process, and size-exclusion chromatographic controls confirmed its efficiency.

Chemical Fractionation↗
PubMed1981

Evaluation of ion exchange resins and various enzymes in thiamine analysis.

Four ion exchange resins and 9 enzyme preparations are evaluated for use in the official AOAC thiamine method because Decalso and Clarase or Mylase P either are no longer available or are available in a form that is not suitable for use in the assay. The enzymes are prepared in the same manner described for Clarase or Mylase P in the AOAC method and are compared with Clarase T300 for their effectiveness in releasing thiamine from thiamine phosphate, and their ability to produce similar results on samples. Rhozyme S is 90-100% as effective as Clarase T300 in both of these respects. The other enzymes tested were not satisfactory. Further study is necessary because Rhozyme S also is no longer manufactured. The ion exchange resins are prepared for use in the manner described for Decalso in the AOAC method. Recoveries of thiamine range from 95 to 100%, using Bio-Rex 70 (hydrogen form) ion exchange resin. The other resins tested were not satisfactory.

Enzymes↗