Method for simultaneous determination for Mo, Ti and W element of uranic fluoride
A technology of uranium hexafluoride and elements, applied in the field of simultaneous determination of Mo, Ti and W in uranium hexafluoride
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0013] Take uranium hexafluoride hydrolyzate containing 1g of uranium in a platinum dish, add 3mL of concentrated nitric acid, and evaporate to near dryness. Add 6 mL of deionized water to slightly heat to dissolve the residue, transfer it to a separatory funnel, wash the platinum dish with 2 mL of deionized water twice, and transfer it to a separatory funnel together. Add 25mL of TBP-xylene mixture (1+2) and shake for 30s. After layering, transfer the water phase to another separatory funnel, repeat the extraction operation once more, and transfer the layered water phase into 25mL volumetric flask. Add 1.0mL of 5mol / L hydrochloric acid, 1×10 -3 mol / L salicyl fluorone 2.5mL, 2×10 -2 mol / L hexadecyltrimethylamine bromide 3.0mL, dilute to the mark with water, shake well, stand still for 20min, take reagent blank as reference, use 1cm cuvette in the wavelength range of 490nm~550nm, measure every 2nm According to the absorbance value of the solution, the calculated contents of ...
Embodiment 2
[0015] Take uranium hexafluoride hydrolyzate containing 1g of uranium in a platinum dish, add 3mL of concentrated nitric acid, and evaporate to near dryness. Add 6 mL of deionized water to slightly heat to dissolve the residue, transfer it to a separatory funnel, wash the platinum dish with 2 mL of deionized water twice, and transfer it to a separatory funnel together. Add 25mL of TBP-xylene mixture (1+2) and shake for 30s. After layering, transfer the water phase to another separatory funnel, repeat the extraction operation once more, and transfer the layered water phase into 25mL volumetric flask. Add 1.0mL of 7mol / L hydrochloric acid, 3×10 -3 mol / L salicyl fluorone 2.5mL, 2×10 -2 mol / L hexadecyltrimethylamine bromide 3.0mL, dilute to the mark with water, shake well, stand still for 30min, take reagent blank as reference, use 1cm cuvette in the wavelength range of 490nm~550nm, measure every 2nm According to the absorbance value of the solution, the calculated contents of ...
Embodiment 3
[0017] Take uranium hexafluoride hydrolyzate containing 1g of uranium in a platinum dish, add 3mL of concentrated nitric acid, and evaporate to near dryness. Add 6 mL of deionized water to slightly heat to dissolve the residue, transfer it to a separatory funnel, wash the platinum dish with 2 mL of deionized water twice, and transfer it to a separatory funnel together. Add 25mL of TBP-xylene mixture (1+2) and shake for 30s. After layering, transfer the water phase to another separatory funnel, repeat the extraction operation once more, and transfer the layered water phase into 25mL volumetric flask. Add 1.0mL of 5mol / L hydrochloric acid, 2×10 -3 mol / L salicyl fluorone 2.5mL, 1×10 -2 mol / L hexadecyltrimethylamine bromide 3.0mL, dilute to the mark with water, shake well, stand still for 40min, take reagent blank as reference, use 1cm cuvette in the wavelength range of 490nm~550nm, measure every 2nm According to the absorbance value of the solution, the calculated contents of ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com