Book Flashcards
What is the distribution coefficient?
the conc. of component in org. phase / conc. of comp. in aqueous phase
What is the distribution coefficient a function of? What is it not a funciton of?
nature of the solvent, temperature, equilibrium cpomosition of the aqueous and organic phases but independent of the amount of either phase
Why can the solvent extract more compoment from aqueous feed?
Because the concentration of component in the aqueous feed is higher than that in the aqueous residue from which the org. phase is in equilibrium with.
What are the 6 principal factors affecting the distribution coefficient value?
- Element being extracted
- Oxidation-reduction potential of aqueous phase
- Nature of solvent
- Conc. of complexing agent
- Conc. of salting agent
- Hydrogen ion conc. in aq. phase
How do we measure the ease or difficulting of separation by fractional extraction?
By alpha which is the ratio of the distribution coefficient of component i divided by the distribution coefficient of comp j.
What needs to be added to fractional extraction flowsheets when we need to extract one more comopment?
a scrubbing and stripping section per component extracted.
What main characteristic the metallic element to be extractable by an organic solvent inmmisicible with water needs to have?
The element must be capable of forming an organic-soluble, electrically neutral complex compound with the solvent or with an added complexing agent.
What are coordination bonds?
sharing of electrons from the complexing agent to complete previously unfilled orbits of the cation.
What is the coordination number?
the number of complexing groups that are attached to the cation.
What needs to happen in terms of distribution coefficients for two elements to be separated?
For them to have different distribution coefficients.
How is Pu separted from U in the purex process?
A reducing agent is added to reduce Pu to Pu3+ which makes it extractable to water while uranium stays in the organic phase?
What agent is used to reduce Pu but not U in PUREX process (an example)?
ferrous salt.
Why are complexing agentes used?
to increase or decrease the Distribution coefficient of a metallic component between aqueous solution and kerosene.
Is the addition of a complexing agent necessary?
In some cases where the metallic component like Zr(No3)4 is not extracted by the kerosene solvent a complexing agent is used as a vessel through the organic phase to extract the component.
What is the effect of adding solutes to the aqueous phase?
Increase distribution coefficient of extractable components.
Why does the distributionc oefficient increases with addition of of a solute as nitrate concentration in aqueou sphase?
Because addition of nitrate ion tends to increase the conc. of unionized uranyl nitrate by shifting the equilibrium to the right of the following equation:
UO2(2+) + 2NO3(-) -> UO2(NO3)2
therefore converting it into a more extractable form.
Does the presence of nitric acid decreases the distribution coefficient of Uranium? Why?
For nitric acid concentrations less than about 5M the uranium distribution coefficient is greater the higher the concentration of acid. Beyond 5M increasing acid conc. will decrease U distributionc oefficient. Below 5M this happens because of the salting effect of nitrate ion.
What are some qualities of a good solvent for the separation of metals by fractional extraction?
- Selective (high ratio of distribution coefficient)
- Good extraction capacity
- It should be readily stripped
- relatively immiscible with water
- Different density from water, low viscosity, and high interfacial tensions
- nonvolatile, nonflammable, nontoxic
- readily purified by fractional distillation
- stable in precesenc of chemical agents used in the process.
What is the ingestion toxicity of mill tailings dominated by? Give two example radioisotopes.
Decay daughters of uranium isotopes such as Th-230 and Ra-226
Is toxicity of the uranium ore high enough to warrant measures?
No, just those in mill tailings.
When does the radiotoxicity of mill tailings start to decrease? Why?
10,000 years because of the decay half-life of Th-230 is 80,000 years which is the most dominant contributor to the radiotoxicity of mill tailings.
How does the toxicity of depleted uranium behave with time? Is the toxicity plateau lower or higher than that of the uranium ore?
At the start, it has relatively low toxicity but as the U isotopes decay, they generate decay daughters which cause U to increase its toxicity with time. The plateau is lower than that in the ore.
What are the 6 main types of radioactivity?
- Alpha Decay
- Beta Decay
- Gamma Emission
- Positron Emission
- Electron Capture
- Spontaneous Fisison
What is the energy of alpha particles in alpha decay?
2 to 8 MeV