Process for the preparation of pure lithium oxide
The invention relates to a process for the production of pure lithium oxide and its use, wherein lithium carbonate is reacted with finely divided, elemental carbon in powder form in the temperature range between 600 and 1200° C., wherein the two reactants are intensively premixed prior to the thermolysis process so that the bulk density of the mixture is reduced by at least 5%, preferably by at least 15%.
1 . A process for the production of lithium oxide from
lithium carbonate with a median particle size (D 50 ) between 2 and 150 μm, determined by laser diffraction, and
elemental carbon in powder form with a median primary particle size (D 50 ) of <1 μm, determined by electron microscopy,
with calcination in a temperature range between 60° and 1200° C.,
characterized in that
prior to the calcination the lithium carbonate and the carbon are combined in a molar ratio of 1:0.1 to 1:1.2 and are mixed and compacted, whereby the carbon particles surround the lithium carbonate particles and form a coating and a bulk density of a resulting mixture is increased by at least 5% compared to a bulk density of a mixture of the lithium carbonate particles and the carbon particles prepared without compaction, the bulk density being determined according to EN ISO 697.
2 . The process according to claim 1 , characterized in that the bulk density of the compacted mixture is increased by at least 15% compared to the bulk density of an uncompacted mixture.
3 . The process according to claim 1 , characterized in that combining and mixing is carried out with compaction in grinding units, rotating intensive mixers or compacting devices.
4 . The process according to claim 1 , characterized in that combining and mixing with compaction take place
a) in rotating intensive mixers with an energy input of 10 to 500 kW/m 3 or
b) in rotor beater, pin or grinding media mills or
c) in a compacting machine.
5 . The process according to claim 1 , characterized in that the calcination is carried out in equipment whose product-facing surfaces are made of materials resistant to high temperatures and corrosion from basic lithium salts, which materials are
a) carbon-based materials, selected from material-graphites and pure carbons with disordered graphite structure, or
b) oxide ceramics or Ce-stabilized ZrO 2 , or
c) non-oxide ceramics or
d) metallic materials containing chromium and/or aluminum.
6 . The process according to claim 5 , characterized in that the calcination is carried out in equipment whose product-facing surfaces are selected from metallic materials selected from
high-temperature resistant Cr- and/or Al-containing nickel-based alloys,
Ni- and Cr-containing austenitic steels,
Low-Ni and/or Ni-free, Cr- and Al-containing ferritic steels or Cr-containing mixed austenitic-ferritic steels,
wherein the chromium content of the metallic materials in the absence of Al (<0.1% by weight) is at least 15% by weight.
7 . The process according to claim 5 , characterized in that the metallic materials contain, in addition to chromium and aluminum, the elements niobium, titanium, tantalum and/or silicon, each in proportions of 0 to 10% by weight.
8 . The process according to claim 5 , characterized in that the metallic materials contain <2 wt. % molybdenum.
9 . The process according to claim 5 , characterized in that the metallic materials comprise high-temperature-resistant black or stainless steels which are provided with a Cr-containing metallic coating on the side facing the product, the chromium content in the coating being at least 10% by weight.
10 . The process according to claim 9 , characterized in that a thickness of the coating, determined by electron microscopy, is at least 5 μm.
11 . The process according to claim 1 , characterized in that the calcination is carried out
under vacuum conditions comprising a negative pressure in a range between 0.01 and 50 mbar (1 to 5000 Pa), or
under overflow conditions, whereby an overflowing gas or gas mixture is inert or substantially inert with respect to carbon at temperatures of >600° C.
12 . The process according to claim 11 , characterized in that the gas or the gas mixture comprises nitrogen, a noble gas or mixtures of inert gases.
13 . The process according to claim 1 , characterized in that the molar ratio of the lithium carbo-nate and the carbon is in the range 1:0.6 to 1:1.1.
14 . The process according to claim 1 , characterized in that the carbon comprises elemental carbons in powder form having a specific surface area (BET) of 10 to 1500 m 2 /g, and a median primary particle size D 5 O<1000 nm.
15 . The process of claim 1 , characterized in that the carbon comprises carbon powder having sulfur contents of <1000 ppm, and residual ash contents of <1000 ppm.
16 . The process according to claim 1 , characterized in that the ratio of the median particle sizes D 50 of a deagglomerated carbon powder to Li 2 CO 3 is in the range between 1:50 to 1:20,000.
17 . The process according to claim 1 , characterized in that the calcination is carried out under moving bed conditions.
18 . The process according to claim 1 , characterized in that the produced lithium oxide is subjected to a decarbonizing purification step in which the produced lithium oxide is contacted with a gas stream comprising oxygen-containing gases or gas mixtures selected from O 2 , CO 2 , H 2 O or mixtures thereof, optionally mixed with further gases inert to carbon, at temperatures of at least 300° C.
19 . The process according to claim 1 , characterized in that the powdered elemental carbon used is unprilled carbon black.