GB/T 14501.6-2008Methods for analysis of uranium hexafluoride - Part 6: Determination of uranium (English PDF)
六氟化铀分析方法 第6部分:铀的测定
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Issued by
SAMR; SAC
Level / Type
National · Recommended
Issue date
September 19, 2008
Implementation date
August 1, 2009
Scope
GB/T 14501.6-2008 is the English-translated version of 六氟化铀分析方法 第6部分:铀的测定.
GB/T 14501.6-2008 is the sixth part of the Chinese national series of analysis methods for uranium hexafluoride, and it covers the determination of uranium itself.
It fixes the operating conditions and the steps of two methods, gravimetry and potentiometric titration, and is used on uranium hexafluoride and on high-purity uranium compounds.
For the gravimetric route it lists the reagents and the apparatus, from a 3 kW high-temperature hydrolysis furnace lined with nickel sheet to a covered 100 mL platinum boat and a balance reading to 0.1 mg, then the procedure: hydrolyse the sample under liquid nitrogen, evaporate the uranyl fluoride solution and ignite it to triuranium octoxide.
Normative annexes add the air buoyancy correction and the sample preparation method. It replaces GB/T 14501.6-1994, was issued on 19 September 2008 and has applied since 1 August 2009.
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Document preview — GB/T 14501.6-2008
National Standard of the People's Republic of China
- ICS
- 27.120.30
- Classification
- F 46
- Replacing
- GB/T 14501.6-1994
Issued by: State Administration for Market Regulation; Standardization Administration of the PRC
Contents
- Foreword
- 1 Scope
- 2 Gravimetric method
Foreword
GB/T 14501 "uranium hexafluoride analysis method" is expected to be divided into six sections.
--- Part 1. Chemical Spectrometry;
--- Part 2. Determination of phosphorus;
--- Part 3. Determination of tungsten, molybdenum, niobium, titanium, zirconium chemical spectroscopy;
--- Part 4. Determination of silicon;
--- Part 5. Determination of titanium;
--- Part 6. Determination of uranium.
This section GB/T 14501 Part 6.
This Part replaces GB/T 14501.6-1994 "Determination of uranium hexafluoride of uranium."
Section compared with the GB/T 14501.6-1994 The main changes are as follows.
--- Technical content by weight, based on the same method, modify some of the statements;
--- Revised technical content potentiometric titration;
--- Remove the appendix "non-volatile impurities mass conversion factor";
--- Added Appendix "Air buoyancy correction" and "uranium hexafluoride sample preparation method."
This section of the Appendix A, Appendix B and Appendix C are normative appendix.
1 Scope
This section provides the main operating conditions and procedures uranium hexafluoride uranium gravimetric and potentiometric titration of the two methods.
This section applies to the determination of uranium hexafluoride of uranium, but also for high-purity uranium compounds precise determination of uranium.
2 Gravimetric method
2.1 Method summary
UF6 samples (8-12) liquefied decimation achieved g, frozen in liquid nitrogen after hydrolysis, evaporated hydrolyzate (uranyl fluoride solution), then After high temperature hydrolysis into Triuranium, composed of eight three uranium oxide to obtain quality and potentiometric titration of the quality factor, calculated six UF uranium content.
2.2 Reagents and Instruments
Unless otherwise indicated in the analysis using only recognized as analytical grade reagents and distilled or deionized water.
2.2.1 Deionized water
2.2.2 Nitric acid solution, 1 + 1
2.2.3 hydrolysis temperature furnace, muffle furnace 3kW, lining 2mm thick nickel sheet (200mm × 115mm × 75mm), and with the steam generator and Connected to the condenser.
2.2.4 with cover platinum platinum boat, 100mL.
2.2.5 Platinum Baotou pliers
2.2.6 PTFE rod
2.2.7 tweezers, length 200mm, fluorine plastic header
2.2.8 Infrared lamp, 275W
2.2.9 Analytical Balance, indexing is 0.1mg.
2.2.10 Wrench, 250mm × 30mm
2.2.11 Oven
2.2.12 Bench vise, 75mm […]
2.3 Procedure
2.3.1 Platinum boat ready
2.3.1.1 Platinum boat (2.2.4) into the nitric acid solution (2.2.2) boiled 10min, then washed with deionized water (2.2.1) rinse.
2.3.1.2 Platinum boat into the high temperature hydrolysis furnace (2.2.3), and burned at 900 °C for 20min.
2.3.1.3 ignited after 40min weighed platinum boat cooling in a dryer, accurate to 0.1mg.
2.3.1.4 5min after weighing, weighing results if two adjacent difference is less than 0.2mg, record results of the second. Otherwise repeat weighing, Until two adjacent weighing result is less than 0.2mg. Platinum boat made of quality m1.
2.3.2 Hydrolysis sample, evaporated to dryness and burning
2.3.2.1 checking samples of uranium hexafluoride, if the sample is yellow, it indicates that the sample moisture, can not be used.
2.3.2.2 The sample tube containing a sample of uranium hexafluoride, into the fume hood standing with a gauze wipe the surface moisture and fixtures, home and dry The balance is more than 3h.
2.3.2.3 Weigh the sample containing uranium hexafluoride sample tube, accurate to 0.1mg, once every 30min said, until two adjacent weighing result
......
This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 15 pages — is available in the English PDF.
Referenced standards
Similar standards
Editions of GB/T 14501.6
| Edition | Title | Revision | Status |
|---|---|---|---|
| GB/T 14501.6-2008 | Methods for analysis of uranium hexafluoride - Part 6: Determination of uranium | current edition | Current |
| GB/T 14501.6-1994 | Methods for analysis of uranium hexafluoride - Part 6: Determination of uranium | previous edition | Superseded |
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Related Standards
GB/T 14501.1-1993 — Spectrochemical determination of boron in uranium hexafluoride
GB/T 14501.3-1993 — Spectrochemical determination of tungsten, molybdenum, niobium, itanium and zirconium in uranium hexafluoride
GB/T 14501.4-1993 — Spectrophotometric determination of silicon in uranium hexafluoride
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