WDC: Advanced System for Characterization of Alpha-Bearing Waste Contained in 200L and 400L Drums: Performances and Lessons Learned From the First Industrial Measurement Campaigns

2007 ◽  
Author(s):  
A. Libens ◽  
M. Vandorpe ◽  
J. M. Cuchet
Keyword(s):  
Limit Of Detection ◽  
Counting Efficiency ◽  
Lessons Learned ◽  
Nuclear Facilities ◽  
Nuclear Operators ◽  
System A ◽  
The Future ◽  
Coincidence Counter ◽  
Short Time

The Waste Drum Characterization installation was originally developed for the assay of alpha-bearing waste in standard 200 l (55 gallons) drums during the dismantling operations of the Siemens mixed-oxide (MOX) facility in Hanau (Germany). That installation was validated and qualified by the German authorities, its main performances being: - Counting efficiency for coincident neutrons: app. 1%; - Lowest Limit of Detection (LLD): 75 mg 240Pueq; - Pu content per drum: up to 100 g tot. (35 g 240Pueq); - Measurement duration: app. 20 minutes. The success of this system, a passive neutron coincidence counter combined with a high resolution gamma spectrometer, led to the radiological characterization and qualification of about 1,700 drums during the period 2001 – 2004. In 2005, after completion of the dismantling operations of the Siemens MOX facility, Tecnubel took over the WDC installation which could be used in the frame of the future dismantling of the Belgonucleaire’s MOX plant in Dessel (Belgium), which can be comparable to the Siemen’s one. This second (and new) life for the WDC means that it must be rigorously retested and validated against the Belgian authorities requirements. Furthermore, and additionally to the future use in the Belgonucleaire’s facility, Tecnubel was faced with new challenges, namely: - Assay of 400 l drums together with the 200 l packages; - Determination of the real LLD taking into account the background in different Belgian nuclear facilities, the determination of a value of ∼5 mg 240Pueq being an objective; - Assay of mixed alpha/beta-gamma wastes; - Transportability of the WDC from one plant to another; - Assistance to different nuclear operators for the licensing of the WDC for their own waste types. This paper describes the installation itself and its performances, presents the difficulties encountered during the new challenge and the results of the performed revalidation tests; it gives the perspectives and objectives on short time as well.

scholarly journals Implementation and application of E-technologies in enterprise environment

2007 ◽  
Vol 55 (3) ◽  
pp. 67-74
Author(s):  
Roman Malo
Keyword(s):  
Short Time Period ◽  
Logical Model ◽  
System A ◽  
Theoretical System ◽  
Time Period ◽  
Business Area ◽  
Basic Concepts ◽  
Short Time ◽  
Base Platform

Nowadays, a problem of an e- technologies’ implementation represents one of the most important questions that are being solved within various subjects from business area. With respect of massive implementation of activities as e- commerce, e- payments and others the e- technologies’ implementation is the progressive way of these subjects’ expansion. However, due to relatively short time period in which enterprise subjects have solved there is a set of vague aspects going together with this problem. The paper analyses the area of e- technologies and defines relations between basic concepts. Following this theoretical system a few hypothesis are constructed and used as a base platform for a determination of the logical model for implementation of e- technologies in enterprise environment.

scholarly journals Development of Lateral Flow Immunochromatographic Assays Using Colloidal Au Sphere and Nanorods as Signal Marker for the Determination of Zearalenone in Cereals

Foods ◽  
2020 ◽  
Vol 9 (3) ◽  
pp. 281 ◽  
Author(s):  
Mingfei Pan ◽  
Tianyu Ma ◽  
Jingying Yang ◽  
Shijie Li ◽  
Shengmiao Liu ◽  
...  
Keyword(s):  
Limit Of Detection ◽  
Fumonisin B1 ◽  
Test Strip ◽  
Food Samples ◽  
Cross Reactivity ◽  
Lateral Flow ◽  
Rapid Screening ◽  
Colloidal Au ◽  
Short Time

This paper describes the development of lateral flow immunochromatographic assays (ICAs) using colloidal Au sphere (SP) and nanorods (NRs) as signal markers for the determination of zearalenone (ZEN) in cereals. The developed ICAs can detect the analyte ZEN within a short time (10 min), and achieve lower limit of detection (LOD). This is the first time that the AuNRs are used as signal probe in immune test strip for ZEN detection. For colloidal AuSP immunochromatographic analysis (AuSP-ICA), the LODs in solution and spiked cereal sample were 5.0 μg L−1 and 60 μg kg−1, and for AuNRs immunochromatographic analysis (AuNRs-ICA) the two LODs achieved 3.0 μg L−1 and 40 μg kg−1, respectively. These two proposed ICAs have minor cross-reaction to the structural analogs of ZEN, and no cross-reactivity with aflatoxin B1, T-2 toxin, ochratoxin A, deoxynivalenol, fumonisin B1. Both of the developed ICAs can specifically and sensitively detect ZEN in cereals, providing an effective strategy for rapid screening and detection of ZEN in a large number of food samples.

scholarly journals Balanced Window Method in 14C Liquid Scintillation Counting

Radiocarbon ◽  
2003 ◽  
Vol 45 (1) ◽  
pp. 113-122 ◽  
Author(s):  
P Theodórsson ◽  
S Ingvarsdottir ◽  
G I Gudjonsson
Keyword(s):  
Liquid Scintillation ◽  
Pulse Height ◽  
Counting Efficiency ◽  
Pulse Height Spectrum ◽  
System A ◽  
Window Method ◽  
Upper Limits ◽  
Long Time ◽  
Counting Window

The authors present a detailed theoretical and experimental study of the liquid scintillation balanced counting method, widely used in radiocarbon dating, using a simple, laboratory-made system. A fixed counting window becomes a balanced window when the high voltage is set where the 14C count rate rises to a maximum. Using a measured 14C pulse height spectrum, we have calculated the lower and upper limits for 11 balanced windows of varying width and their respective counting efficiencies. Furthermore, we have studied: (1) theoretically and experimentally, the counting efficiency for up to a ±15% shift in pulse height from the balanced setting, (2) the change in pulse height due to temperature variations, (3) the long-time stability of the system, and (4) a method that allows a quick determination of the balance voltage for individual samples, using the Compton spectrum of 133Ba. The standard deviation for thirty 24-hr measuring periods for a 14C standard (190 Bq) was within the expected statistical standard error (0.03%).

The determination of technetium-99 in urine

1983 ◽  
Vol 61 (9) ◽  
pp. 1949-1951 ◽  
Author(s):  
Gary H. Kramer
Keyword(s):  
Ion Exchange ◽  
Organic Solvent ◽  
Human Urine ◽  
Liquid Scintillation ◽  
Limit Of Detection ◽  
Counting Efficiency ◽  
Radiochemical Analysis ◽  
Gas Proportional Counter ◽  
Counting Time

A method has been developed for the routine radiochemical analysis of technetium-99 in human urine. The excreted technetium is coprecipitated from a 200 mL urine sample with CuS. Valence state adjustments are performed with K2S2O8. The precipitate is dissolved in ammoniacal peroxide and, after the Cu(II) is removed by ion exchange, the Tc-99 is extracted with 2-butanone (MEK). Subsequent evaporation of the organic solvent gives an essentially weightless source that if counted with a gas proportional counter will give a better limit of detection than liquid scintillation methods. The recovery of Tc-99 using this procedure is 80% (σ = 4%) and the limit of detection is 20 mBq (0.6 pCi) at the 95% confidence level for a routine sample – counting time 20 minutes, counting efficiency 24%, ambient background 1.3 counts per minute (cpm).

International determination of the total motion of the pole

1961 ◽  
Vol 13 ◽  
pp. 29-41
Author(s):  
Wm. Markowitz
Keyword(s):  
Secular Motion ◽  
The Future

A symposium on the future of the International Latitude Service (I. L. S.) is to be held in Helsinki in July 1960. My report for the symposium consists of two parts. Part I, denoded (Mk I) was published [1] earlier in 1960 under the title “Latitude and Longitude, and the Secular Motion of the Pole”. Part II is the present paper, denoded (Mk II).

Interpreting Open- and Closed-Loop Transfer Relations Between Cardiorespiratory Parameters: Lessons Learned from a Computer Model of Beat-to-Beat Cardiovascular Regulation

1997 ◽  
Vol 36 (04/05) ◽  
pp. 237-240
Author(s):  
P. Hammer ◽  
D. Litvack ◽  
J. P. Saul
Keyword(s):  
Computer Model ◽  
Closed Loop ◽  
Computer Models ◽  
Cardiovascular Regulation ◽  
Cardiovascular Control ◽  
Lessons Learned ◽  
Multiple Systems ◽  
Response Characteristics ◽  
Similarities And Differences

Abstract:A computer model of cardiovascular control has been developed based on the response characteristics of cardiovascular control components derived from experiments in animals and humans. Results from the model were compared to those obtained experimentally in humans, and the similarities and differences were used to identify both the strengths and inadequacies of the concepts used to form the model. Findings were confirmatory of some concepts but contrary to some which are firmly held in the literature, indicating that understanding the complexity of cardiovascular control probably requires a combination of experiments and computer models which integrate multiple systems and allow for determination of sufficiency and necessity.

SERUM TRIIODOTHYRONINE DETERMINATION BY SATURATION ANALYSIS

1973 ◽  
Vol 72 (4) ◽  
pp. 714-726 ◽  
Author(s):  
A. Burger ◽  
B. Miller ◽  
C. Sakoloff ◽  
M. B. Vallotton
Keyword(s):  
Ionic Strength ◽  
Limit Of Detection ◽  
Improved Method ◽  
Accuracy Of Measurement ◽  
Tracer Amount ◽  
The Mean ◽  
Physiological Values ◽  
Hyperthyroid Patients ◽  
Solvent Blank

ABSTRACT An improved method for the determination of serum triiodothyronine (T3) has been developed. After addition of a tracer amount of the hormone, T3 was extracted from 1 ml serum under conditions of pH and ionic strength which favoured T3 extraction (89%) over thyroxine (T4) extraction (58%). Chromatography of the extracted material on Sephadex LH-20 separated T3 completely from residual T4. The T3 eluate was dried, then re-dissolved in 0.5 ml NaOH 0.04 n. To 0.2 ml duplicate aliquots, a standard amount of TBG was added for the competitive protein analysis. After one hour incubation at 4°C, separation of bound from free T3 was achieved on small Sephadex G-25 columns. Overall recovery was 67 ± 10.8% and correction for the loss was made. The solvent blank was 37 ± 27 (sd) ng/100 ml. Accuracy of measurement of known quantities of T3 added to serum was 98.4%. The coefficient of variation within the assay was 6.2% and between the assays it was 11.4%. The limit of detection (0.1 ng) corresponded to a concentration of 25 ng/100 ml. T4 added to serum did not interfere with T3 determination until high non-physiological values were reached. The mean ± sd serum T3 in 54 euthyroid subjects was 153 ± 58 ng/100 ml and in 24 hyperthyroid patients it was 428 ±186 ng/100 ml; 4 out of the 24 hyperthyroid values were within 2 sd of the mean euthyroid group. All the values found in the euthyroid group were well above the limit of detection of the method.

Adapting Tactical Military Structures to the Current and Future Operational Environments

2020 ◽  
Vol 26 (1) ◽  
pp. 157-162
Author(s):  
Paul Tudorache ◽  
Lucian Ispas
Keyword(s):  
Best Practices ◽  
Lessons Learned ◽  
Organizational Adaptation ◽  
Common Denominator ◽  
Military Operations ◽  
The Future ◽  
Military Units

AbstractUsing the lessons learned from recent military operations such as Operation Inherent Resolve (OIR) from Syria and Iraq, we proposed to investigate the need for tactical military units to adapt operationally to grapple with the most common requirements specific to current operational environments, but also for those that can be foreseen in the future. In this regard, by identifying the best practices in the field that can be met at the level of some important armies, such as USA and UK, we will try to determine a common denominator of most important principles whose application may facilitate both operational and organizational adaptation necessary for tactical military units to perform missions and tasks in the most unknown future operational environments.

Spectrophotometeric Determination of Trifluoperazine HCL in Pure Forms and Pharmaceutical Preperations

2017 ◽  
Vol 9 (5) ◽  
Author(s):  
Mohammad Hamzah Hamzah ◽  
Rawa M M Taqi ◽  
Muna M. Hasan ◽  
Raid J. M. Al-Timimi
Keyword(s):  
Standard Method ◽  
Limit Of Detection ◽  
Molar Absorptivity ◽  
Dosage Forms ◽  
Oxidizing Agent ◽  
Optimum Conditions ◽  
Limit Of Quantification ◽  
Cerium Ion ◽  
Blank Solution

A simple and accurate spectrophotometric method for the determination of Trifluoperazine HCl in pure and dosage forms was developed. The method is based on the reaction between Trifluoperazine HCl and p-chloroaniline in the presence of cerium ion as oxidizing agent which lead to the formation of violate color product that absorbed at a maximum wavelength 570nm while the blank solution was pink. Under the optimum conditions a linear relationship between the intensity and concentration of TRF in the range 4-50μg/ml was obtained . The molar absorptivity 3.74×103 L.mol-1.cm-1 , Limit of detection (2.21μg/ml), while limit of quantification was 7.39μg/ml. The proposed analytical method was compared with standard method using t-test and F-test , the obtained results shows there is no significant differences between proposed method and standard method. Based on that the proposed method can be used as an alternative method for the determination of TRF in pure and dosage forms.

Fast Method for the Determination of Residual Solvents in Radiopharmaceutical Products

2017 ◽  
Vol 68 (4) ◽  
pp. 666-670 ◽  
Author(s):  
Mirela Mihon ◽  
Catalin Stelian Tuta ◽  
Alina Catrinel Ion ◽  
Dana Niculae ◽  
Vasile Lavric
Keyword(s):  
Gas Chromatography ◽  
Control Method ◽  
Limit Of Detection ◽  
The Body ◽  
Biologically Active ◽  
Injection Technique ◽  
Fast Method ◽  
Residual Solvent ◽  
Residual Solvents

The aim of this work was the development and validation of a fast analytical method to determine the residual solvents content in radiopharmaceuticals such as: 18F-Fluorodeoxyglucose (18F-FDG), 18F-Fluoroestradiol (18F-FES), 18F-Fluorothymidine (18F-FLT),18F-Fluoromisonidazole (18F-FMISO). Radiopharmaceuticals are radioactive preparations for medical purposes used in nuclear medicine as tracers in diagnostic imaging and treatment of certain diseases. Positron Emission Tomography (PET) is a medical imaging technique that consists in introducing into the body of a small amount of a biologically active chemical compound labelled with a short lived positron-emitting radioisotope (18F, 11C, 68Ga). Residual solvents are critical impurities in radiopharmaceuticals that can affect labelling, stability and physicochemical properties of drugs. Therefore, the determination of these solvents is essential for quality control of radiopharmaceuticals. Validation of the control method for residual solvents by gas chromatography is referred by the European Pharmacopoeia using a special injection technique (head space). The parameters of the method, which comply with International Conference on Harmonization guidelines, are: accuracy, precision, linearity, limit of detection, limit of quantification and robustness. The proposed method (direct gas chromatography injection) proved to be linear, precise, accurate and robust. Good linearity was achieved for all the solvents and correlation coefficients (R2) for each residual solvent were found more than 0.99.

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