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A separatory funnel used for liquid–liquid extraction, as evident by the two immiscible liquids.. Liquid–liquid extraction, also known as solvent extraction and partitioning, is a method to separate compounds or metal complexes, based on their relative solubilities in two different immiscible liquids, usually water (polar) and an organic solvent (non-polar).
The lanthanides become harder as the series is traversed: as expected, lanthanum is a soft metal. Lanthanum has a relatively high resistivity of 615 nΩm at room temperature; in comparison, the value for the good conductor aluminium is only 26.50 nΩm. [28] [29] Lanthanum is the least volatile of the lanthanides. [30]
Organolanthanide chemistry is the field of chemistry that studies organolanthanides, compounds with a lanthanide-carbon bond. Organolanthanide compounds are different from their organotransition metal analogues in the following ways: They are far more air- and water-sensitive and are often pyrophoric.
Boiling tea leaves in water extracts the tannins, theobromine, and caffeine out of the leaves and into the water, as an example of a solid-liquid extraction. Decaffeination of tea and coffee is also an example of an extraction, where the caffeine molecules are removed from the tea leaves or coffee beans, often utilising supercritical fluid ...
The lighter (larger) lanthanides adopt a hexagonal 7-coordinate structure while the heavier/smaller ones adopt a cubic 6-coordinate "C-M 2 O 3" structure. [11] All of the sesquioxides are basic, and absorb water and carbon dioxide from air to form carbonates, hydroxides and hydroxycarbonates. [7] They dissolve in acids to form salts. [8]
Acid–base extraction is a subclass of liquid–liquid extractions and involves the separation of chemical species from other acidic or basic compounds. [1] It is typically performed during the work-up step following a chemical synthesis to purify crude compounds [2] and results in the product being largely free of acidic or basic impurities.
Lanthanide oxides: clockwise from top center: praseodymium, cerium, lanthanum, neodymium, samarium and gadolinium. The chemistry of the lanthanides is dominated by the +3 oxidation state, and in Ln III compounds the 6s electrons and (usually) one 4f electron are lost and the ions have the configuration [Xe]4f (n−1). [23]
Lanthanide and actinide aqua ions have higher solvation numbers (often 8 to 9), with the highest known being 11 for Ac 3+. The strength of the bonds between the metal ion and water molecules in the primary solvation shell increases with the electrical charge, z, on the metal ion and decreases as its ionic radius, r, increases. Aqua ions are ...