scholarly journals Low Level Waste Treatment by Ion-Exchange, II. Use of a Weak Acid, Carboxylic-&Henolic Ion-Exchange Resin

1961 ◽  
Author(s):  
R. R. Holcomb ◽  
J. T. Roberts
Keyword(s):  
Ion Exchange ◽  
Waste Treatment ◽  
Exchange Resin ◽  
Ion Exchange Resin ◽  
Weak Acid ◽  
Low Level

Identification of Possible High Integrity Containers for Low-Level Nuclear Waste Disposal

1981 ◽  
Vol 6 ◽  
Author(s):  
Jeffrey D. Williams
Keyword(s):  
South Carolina ◽  
Structural Integrity ◽  
Exchange Resin ◽  
Ion Exchange Resin ◽  
Economic Factors ◽  
Burial Site ◽  
Low Level ◽  
High Integrity ◽  
Low Level Radioactive Waste ◽  
Selection Of

ABSTRACTIncreased concern by the State of South Carolina over the condition and capacity of the low-level radioactive waste burial site at Barnwell has prompted them to promulgate new regulations on waste burial containers. As of September 30, 1981, ion exchange resin and filter media waste with an activity of 1 μCi/cc or greater and with isotopes with halflives greater than five years disposed at Barnwell shall be solidified or confined in a “high integrity container”. The materials and designs of these containers are required to provide waste isolation from the environment for a period of 300 years and provide the structural integrity specified in 49 CFR 173.398(b). HITTMAN has been active in the design and development of containers suitable for this purpose with this paper detailing the analyses involved. Material selections were limited to stainless steel, fiberglass, and polyethylenes. Structural concerns focused on overpressure requirements, drop-testing requirements, and lifting capabilities. With a lifetime dose of up to 108 rads, the possibilities of radiation damage were considered. Preliminary selection of polyethylene was based on satisfactory resolution of these issues and economic factors.

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.

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