An Improved Method for Operating Ion-Exchange Resin Columns in Separating.the Rare-Earth Elements

1955 ◽  
Vol 59 (8) ◽  
pp. 690-695 ◽  
Author(s):  
Walter E. Nervik
Keyword(s):  
Rare Earth ◽  
Ion Exchange ◽  
Rare Earth Elements ◽  
Exchange Resin ◽  
Ion Exchange Resin ◽  
Improved Method

Speciation of a lanthanide (Sm) using an ion exchange resin

2016 ◽  
Vol 8 (37) ◽  
pp. 6774-6781 ◽  
Author(s):  
Ildephonse Nduwayezu ◽  
Fatemeh Mostafavirad ◽  
Madjid Hadioui ◽  
Kevin J. Wilkinson
Keyword(s):  
Rare Earth ◽  
Ion Exchange ◽  
Environmental Samples ◽  
Exchange Resin ◽  
Rare Earth Metals ◽  
Ion Exchange Resin ◽  
Exchange Technique ◽  
The Rare Earth

An ion exchange technique has been developed to enable speciation measurements of the rare earth metals in environmental samples.

OPTIMIZATION OF DNA EXTRACTION METHODS FROM BIOLOGICAL MATERIALS OF HONEY BEES IN A DIFFERENT METAMOTPHOSIS PHASE

2016 ◽  
Vol 52 ◽  
pp. 171-176
Author(s):  
M. Palkina ◽  
O. Metlitska
Keyword(s):  
Ion Exchange ◽  
Dna Extraction ◽  
Honey Bees ◽  
Biological Material ◽  
Exchange Resin ◽  
Ion Exchange Resin ◽  
Extraction Methods ◽  
Chelex 100 ◽  
Drone Brood ◽  
Dna Extraction Methods

The aim of the research – adaptation, optimization and using of existing DNA extraction methods from bees’ biological material with the reagent «Chelex-100" under complex economic conditions of native laboratories, which will optimize labour costs and improve the economic performance of DNA extraction protocol. Materials and methods. In order to conduct the research the samples of honey bees’ biological material: queen pupae exuviae, larvae of drone brood, some adult bees’ bodies (head and thorax) were selected. Bowl and drone brood were obtained from the experimental bee hives of Institute of Apiculture nd. a. P. I. Prokopovich of NAAS. DNA extraction from biosamples of Apis mellifera ssp. was carried out using «Chelex-100®» ion exchange resin in different concentrations and combinations. Before setting tests for determination of quantitative and quality indexes, dilution of DNA samples of the probed object was conducted in ratio 1:40. The degree of contamination with protein and polysaccharide fractions (OD 260/230), quantitative content of DNA (OD 260/280) in the extracted tests were conducted using spectrophotometer of «Biospec – nano» at the terms of sample volume in 2 µl and length of optical way in 0,7 mm [7]. Verification of DNA samples from biological material of bees, isolated by «Chelex-100®», was conducted after cold keeping during 24 hours at 20°C using PСR with primaries to the fragment of gene of quantitative trait locus (QTL) Sting-2 of next structure [8]:  3' – CTC GAC GAG ACG ACC AAC TTG – 5’; 3' – AAC CAG AGT ATC GCG AGT GTT AC – 5’ Program of amplification: 94 °C – 5 minutes – 1 cycle; 94 °C – 1 minute, 57°C – 1 minute, 72 °C – 2 minutes – 30 cycles; elongation after 72°C during 2 minutes – 1 cycle. The division of obtained amplicons was conducted by gel electrophoresis at a low current – 7 µÀ, in 1,5 % agarose gel (Sigma ®) in TAE buffer [7]. The results. At the time of optimization of DNA isolation methods, according to existing methods of foreign experts, it was found optimal volume of ion exchange resin solution was in the proposed concentration: instead of 60 µl of solution used 120 µl of «Chelex-100®», time of incubation was also amended from 30 minutes to 180 minutes [9]. The use of the author's combination of method «Chelex-100®» with lysis enzymes, proteinase K and detergents (1M dithiothreitol), as time of incubation was also amended, which was reduced to 180 minutes instead of the proposed 12 hours [10]. Changes in quality characteristics of obtained DNA in samples after reduction in incubation time were not found. Conclusions. The most economical method of DNA isolation from bees’ biological material is 20% solution of «Chelex-100» ion exchange resin with the duration of the incubation period of 180 minutes. It should also be noted that the best results can be obtained from exuviae, selected immediately after the queen’s exit from bowl, that reduces the likelihood of DNA molecules destruction under the influence of nucleases activation, but not later than 12 hours from release using the technology of isolated obtain of queens.

Chromatography of chlorinated biphenyls on an ion-exchange resin

1977 ◽  
Vol 49 (6) ◽  
pp. 764-766 ◽  
Author(s):  
Toshihiko. Hanai ◽  
Harold F. Walton
Keyword(s):  
Ion Exchange ◽  
Exchange Resin ◽  
Ion Exchange Resin

scholarly journals Two-Step Solvent Extraction of Radioactive Elements and Rare Earths from Estonian Phosphorite Ore Using Nitrated Aliquat 336 and Bis(2-ethylhexyl) Phosphate

Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 388
Author(s):  
Silvester Jürjo ◽  
Liis Siinor ◽  
Carolin Siimenson ◽  
Päärn Paiste ◽  
Enn Lust
Keyword(s):  
Rare Earth ◽  
Solvent Extraction ◽  
Rare Earth Elements ◽  
Toxic Elements ◽  
Downstream Processing ◽  
Liquid Extraction ◽  
Aliquat 336 ◽  
Radioactive Elements ◽  
Improved Method ◽  
Ph Values

Estonian phosphorite ore contains trace amounts of rare earth elements (REEs), many other d-metals, and some radioactive elements. Rare earth elements, Mo, V, etc. might be economically exploitable, while some radioactive and toxic elements should be removed before any other downstream processing for environmental and nutritional safety reasons. All untreated hazardous elements remain in landfilled waste in much higher concentration than they occur naturally. To resolve this problem U, Th, and Tl were removed from phosphorite ore at first using liquid extraction. In the next step, REE were isolated from raffinate. Nitrated Aliquat 336 (A336[NO3]) and Bis(2-ethylhexyl) Phosphate (D2EHPA) were used in liquid extraction for comparison. An improved method for exclusive separation of radioactive elements and REEs from phosphorite ore in 2-steps has been developed, exploiting liquid extraction at different pH values.

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