Origins of Clustering of Metalate-Extractant Complexes in ...
THE ACID GENERATED IN THE TANKHOUSE IS RETURNED IN COPPER=Different Types of Extractant
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Transcript of THE ACID GENERATED IN THE TANKHOUSE IS RETURNED IN COPPER=Different Types of Extractant
THE ACID GENERATED IN THE TANKHOUSE IS RETURNED IN COPPER-DEPLETED ELECTROLYTE TO STRIP MORE COPPER FROM THE CIRCULATING LOADED ORGANIC SOLUTION THE ORGANIC REAGENT IS REGENERATED DURING THE STRIPPING PROCESS AND IS RETURNED TO THE EXTRACTION SECTION TO EXTRACT MORE COPPER
Extraction CuSO4(aq) + 2LH(org) 10487741048774CuL2(org) + 2H+(aq)
Stripping CuL2(org) + 2H+(aq) 10487741048774CuSO4(aq) + 2LH(org)
Equilibrium constant (K) = [CuL 2 ] [H + ] 2
[CuSO4] [LH]2
Distribution (D) = Cu(org) is given
Cu(aq) by Log D = Log K = 2 Log [LH] + 2pH
Mode of Operation
Cross-Current Operation
Crosscurrent mode is mostly used in batch operation Batch extractors have traditionally
been used in low capacity multi-product plants such as are typical in the pharmaceutical
and agrochemical industries For washing and neutralization operations that require very
few stages crosscurrent operation is particularly practical and economical and offers a
great deal of flexibility The extraction equipment is usually an agitated tank that may
also be used for the reaction steps
In these tanks solvent is first added to the feed the contents are mixed settled and then
separated Single stage extraction is used when the extraction is fairly simple and can be
achieved without a high amount of solvent If more than one stage is required multiple
solvent-washes are given
Though operation in crosscurrent mode offers more flexibility it is not very desirable due
to the high solvent requirements and low extraction yields
Counter-Current Operation
For larger volume operation and more efficient use of solvent countercurrent mixersettlers
or columns are employed Countercurrent operation conserves the mass transfer
driving force and hence gives optimal performance
The dimensionless term mSF included in all the above equations is called the extraction
factor (E) and is an important parameter in the design of extraction processes For a
given number of stages the higher the E factor the higher is the reduction ratio and
easier is the extraction Systems with E of less than 13 are not likely to be commercially
feasible
Different Types of Extractant
Different Types of Extractants determine how well the extraction yield It affect the time taken the solubility pH values and selectivity(product purity) Below are 5 main extractants and its advantages and uses Extractants are used because it is necessary to form a chemical compound (= complex) with the solute and thus make it soluble in the organic phase
Chelating Agents
bull Main commercial extractants for copper
bull Operate on hydrogen ion cycle
bull Function with acid and ammoniacal leach solutions
bull More selective than other extractant classes
bull Kinetically slower than ion pair extractants
bull Have good physical properties in terms of phase separation low aqueous solubility
chemical stability
Ions-Pair Extractants
bull Commercial extractants for uranium thorium vanadium gold cobalt and other metals
bull Kinetics both extraction and stripping are fast
bull Extraction is usually of a metal anion complex
bull Selectivity is not high Other anions can compete with the metal being extracted
bull Selectivity can be pH dependent
Neutral Solvating Extractants
bull Kinetically fast
bull Extract neutral metal complexes
bull Selectivity is low
bull Organometallic complex must be organic soluble
Organic Acid Extractants
bull Operate on a hydrogen ion cycle but do not display hydrogen ion stoichiometry
bull Selectivity is poor and careful pH control may be required to achieve reasonable
selectivity
Ligand Subtitution Extractants
bull Extraction is not pH sensitive
bull Stripping(transfer of the metal back into a second pure aqueous phase for winning or
further processing) is by decomposition of the metal ligand chloride complex at relatively
low chloride ion
concentration
bull Selectivity can be very high and is based to an extent on extraction kinetics
separated Single stage extraction is used when the extraction is fairly simple and can be
achieved without a high amount of solvent If more than one stage is required multiple
solvent-washes are given
Though operation in crosscurrent mode offers more flexibility it is not very desirable due
to the high solvent requirements and low extraction yields
Counter-Current Operation
For larger volume operation and more efficient use of solvent countercurrent mixersettlers
or columns are employed Countercurrent operation conserves the mass transfer
driving force and hence gives optimal performance
The dimensionless term mSF included in all the above equations is called the extraction
factor (E) and is an important parameter in the design of extraction processes For a
given number of stages the higher the E factor the higher is the reduction ratio and
easier is the extraction Systems with E of less than 13 are not likely to be commercially
feasible
Different Types of Extractant
Different Types of Extractants determine how well the extraction yield It affect the time taken the solubility pH values and selectivity(product purity) Below are 5 main extractants and its advantages and uses Extractants are used because it is necessary to form a chemical compound (= complex) with the solute and thus make it soluble in the organic phase
Chelating Agents
bull Main commercial extractants for copper
bull Operate on hydrogen ion cycle
bull Function with acid and ammoniacal leach solutions
bull More selective than other extractant classes
bull Kinetically slower than ion pair extractants
bull Have good physical properties in terms of phase separation low aqueous solubility
chemical stability
Ions-Pair Extractants
bull Commercial extractants for uranium thorium vanadium gold cobalt and other metals
bull Kinetics both extraction and stripping are fast
bull Extraction is usually of a metal anion complex
bull Selectivity is not high Other anions can compete with the metal being extracted
bull Selectivity can be pH dependent
Neutral Solvating Extractants
bull Kinetically fast
bull Extract neutral metal complexes
bull Selectivity is low
bull Organometallic complex must be organic soluble
Organic Acid Extractants
bull Operate on a hydrogen ion cycle but do not display hydrogen ion stoichiometry
bull Selectivity is poor and careful pH control may be required to achieve reasonable
selectivity
Ligand Subtitution Extractants
bull Extraction is not pH sensitive
bull Stripping(transfer of the metal back into a second pure aqueous phase for winning or
further processing) is by decomposition of the metal ligand chloride complex at relatively
low chloride ion
concentration
bull Selectivity can be very high and is based to an extent on extraction kinetics
Chelating Agents
bull Main commercial extractants for copper
bull Operate on hydrogen ion cycle
bull Function with acid and ammoniacal leach solutions
bull More selective than other extractant classes
bull Kinetically slower than ion pair extractants
bull Have good physical properties in terms of phase separation low aqueous solubility
chemical stability
Ions-Pair Extractants
bull Commercial extractants for uranium thorium vanadium gold cobalt and other metals
bull Kinetics both extraction and stripping are fast
bull Extraction is usually of a metal anion complex
bull Selectivity is not high Other anions can compete with the metal being extracted
bull Selectivity can be pH dependent
Neutral Solvating Extractants
bull Kinetically fast
bull Extract neutral metal complexes
bull Selectivity is low
bull Organometallic complex must be organic soluble
Organic Acid Extractants
bull Operate on a hydrogen ion cycle but do not display hydrogen ion stoichiometry
bull Selectivity is poor and careful pH control may be required to achieve reasonable
selectivity
Ligand Subtitution Extractants
bull Extraction is not pH sensitive
bull Stripping(transfer of the metal back into a second pure aqueous phase for winning or
further processing) is by decomposition of the metal ligand chloride complex at relatively
low chloride ion
concentration
bull Selectivity can be very high and is based to an extent on extraction kinetics
bull Stripping(transfer of the metal back into a second pure aqueous phase for winning or
further processing) is by decomposition of the metal ligand chloride complex at relatively
low chloride ion
concentration
bull Selectivity can be very high and is based to an extent on extraction kinetics