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Patent 2265183 Summary

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Claims and Abstract availability

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(12) Patent: (11) CA 2265183
(54) English Title: MAGNESIUM METAL PRODUCTION
(54) French Title: PRODUCTION DE MAGNESIUM METALLIQUE
Status: Expired and beyond the Period of Reversal
Bibliographic Data
Abstracts

English Abstract


Magnesium metal is produced by electrolysis of magnesium chloride
employing a high surface area anode, for example, a porous anode to which
hydrogen gas is fed. Hydrogen chloride is formed from the chloride ions at the
anode, rather than chlorine gas; the process also has the advantage of
operating
at a lower voltage with a lower energy requirement than the conventional
process in which chlorine gas is generated at the anode.


Claims

Note: Claims are shown in the official language in which they were submitted.


-6-
CLAIMS
1. In a process for the electrolytic production of magnesium from
magnesium chloride in an electrolytic cell having an anode and a cathode, and
in which magnesium is generated at the cathode, the improvement wherein
hydrogen gas is fed to the anode and hydrogen chloride is formed in situ at
the
anode.
2. A process according to claim 1, wherein the anode is a high surface area
anode.
3. A process according to claim 1, wherein the anode is a porous anode and
the hydrogen gas permeates the pores of the anode.
4. A process according to claim 1, wherein said magnesium chloride is
dissolved in a molten salt electrolyte in said cell, said anode is a porous
anode
and the molten electrolyte permeates the pores of the porous anode.
5. A process according to claim 1, 2, 3 or 4, wherein the anode is of
graphite, silicon carbide or silicon nitride.
6. A process for the electrolytic production of magnesium comprising:
i) ~electrolysing magnesium chloride in a molten salt
electrolyte in an electrolysis cell having a cathode and an
anode, with formation of magnesium metal at said cathode,
ii) ~feeding hydrogen gas to said anode and reacting chloride
ions at said anode with the hydrogen gas to form hydrogen
chloride,
iii) ~recovering the magnesium metal from said cell, and
iv) ~recovering the hydrogen chloride from said cell.

-7-
7. A process according to claim 6, wherein said cell is operated at a cell
voltage lower than the cell voltage of a corresponding cell having a carbon
anode, without hydrogen gas, in which chlorine gas is developed at the anode.
8. A process according to claim 6 or 7, wherein said anode is a high
surface area anode.
9. A process according to claim 6 or 7, wherein said anode is a porous
anode and the hydrogen gas permeates from the pores of the anode into the
cell.
10. A process according to claim 6 or 7, wherein said anode is a porous
anode and the molten electrolyte permeates the pores of the porous anode.
11. A process according to claim 6, 7, 8, 9 or 10, wherein said anode is of
graphite, silicon carbide or silicon nitride
12. An electrolytic cell for production of magnesium metal from magnesium
chloride comprising:
a) ~a cell for housing magnesium chloride in a molten salt
electrolyte, said cell having a cathode and an anode,
b) ~means for feeding hydrogen gas to said anode,
c) ~means for recovery from said cell of magnesium metal
developed at said cathode, and
d) ~means for recovery from said cell of hydrogen chloride
developed at said anode.

-8-
13. A cell according to claim 12, further including a conduit for delivery of
hydrogen gas to said anode.
14. A cell according to claim 12 or 13, wherein said anode is a high surface
area anode.
15 A cell according to claim 12 or 13, wherein said anode is a porous
anode.
16. A cell according to claim 12, 13, 14 or 15, wherein said anode is of
graphite, silicon carbide or silicon nitride
17. Use of hydrogen in an electrolytic cell for the production of magnesium
from magnesium chloride with production of by-product hydrogen chloride at
the anode.

Description

Note: Descriptions are shown in the official language in which they were submitted.


CA 02265183 2006-12-07
- 1 -
This invention relates to production of magnesium by electrolysis.
Conventional electrolytic production of magnesium from magnesium
chloride dissolved in a molten salt electrolyte in an electrolytic cell
results in
formation of magnesium at the cathode and chlorine gas at the cathode. The
molten salt electrolyte typically comprises one or more alkali metal or
alkaline
earth metal chlorides in which the magnesium chloride is dissolved.
The production of chlorine as a by-product of the production of
magnesium requires auxiliary equipment for recovery and storage of the by-
product chlorine gas which typically is reacted with hydrogen gas to form
hydrochloric acid. Electrolytic methods for producing magnesium are
described in U.S. Patents 4,073,703; 4,192,724; 5,089,094 and 5,665,220. :
This invention seeks to provide a new electrolytic process for the
production of magnesium from magnesium chloride, in which hydrogen
chloride is produced as the by-product.
This invention also seeks to provide a new electrolytic process for the
production of magnesium from magnesium chloride at a lower energy
requirement.
In accordance with one aspect of the invention there is provided in a
process for the electrolytic production of magnesium from magnesium chloride
in an electrolytic cell having an anode and a cathode, and in which magnesium
is generated at the cathode, the improvement wherein hydrogen gas is fed to
the
anode and hydrogen chloride is formed in situ at the anode.
In accordance with another aspect of the invention there is provided a
process for the electrolytic production of magnesium comprising: i)
electrolysing magnesium chloride in a molten salt electrolyte in an
electrolysis
cell having a cathode and an anode, with formation of magnesium metal at said
cathode, ii) feeding hydrogen gas to said anode and reacting chloride ions at
said anode with the hydrogen gas to form hydrogen chloride, iii) recovering
the

CA 02265183 1999-03-11
-2-
magnesium metal from said cell, and iv) recovering the hydrogen chloride from
said cell.
In accordance with still another aspect of the invention there is provided
an electrolytic cell for production of magnesium metal from magnesium
chloride comprising: a) a cell for housing magnesium chloride in a molten salt
electrolyte, said cell having a cathode and an anode, b) means for feeding
hydrogen gas to said anode, c) means for recovery from said cell of
magnesium metal developed at said cathode, and d) means for recovery from
said cell of hydrogen chloride developed at said anode.
In accordance with yet another aspect of the invention there is provided
use of hydrogen in an electrolytic cell for the production of magnesium from
magnesium chloride with production of by-product hydrogen chloride at the
anode.
In particular the anode is a high surface area anode, for example, a
porous anode in which case the hydrogen gas permeates the pores of the anode,
such as by diffusion, or molten electrolyte containing the magnesium chloride
permeates the pores of the anode, to provide the contact between the hydrogen
gas and the chloride ions. The hydrogen gas may be fed along a non-porous
tube or conduit to the porous anode. If this tube or conduit is in contact
with
the bath it should not be of a material which will function as an anode for
the
electrolysis.
As an alternative to a porous anode, any anode having a structure
permitting delivery of hydrogen to the cell bath at the anode may be employed,
for example, an anode having drilled channels for communication with a source
of hydrogen gas. The requirement is that the anode structure deliver hydrogen
gas to the cell bath at the anode, so that chloride ions at the anode react
with the
hydrogen gas to form hydrogen chloride, rather than discharging as chlorine
gas.

CA 02265183 1999-03-11
-3-
By way of example, suitable anodes may be of graphite, silicon carbide
or silicon nitride.
It has been found that introducing hydrogen at the anode in the
electrolytic cell for magnesium metal production results in a lower energy
requirement for the cell, and the cell can be operated at a cell voltage lower
than the cell voltage of a corresponding cell having a conventional carbon or
graphite anode, without hydrogen gas.
In addition it is found that hydrogen chloride is formed directly at the
anode by the reaction:
2C1- + H2(g) = 2HChg) + 2e
where (g) indicates the gas phase.
Furthermore, the method has the advantage that this hydrogen chloride
gas is produced with minimal, if any, production of chlorine gas.
In conventional cells in which chlorine gas is produced as the by-
product, the anode is graphite, and at the high temperatures of operation some
chlorinated hydrocarbons are produced by reaction between the chlorine gas
and the carbon anode, and this presents environmental problems. Eliminating
production of chlorine gas in the present invention can be expected to
alleviate
these problems.
Table I below shows how the decomposition voltage of the electrolysis
decreases, with the process of the invention, as compared with the
conventional
process and how the minimum voltage required to maintain energy balance
changes.

CA 02265183 1999-03-11
-4-
TABLE I
Reaction E Eadiab. Eadiab. - E
MgC12 4 Mg + C12 2.50 3.60 1.1
MgCl2 + H2 4 Mg + HCI 1.46 2.74 1.28
Difference -1.04 -0.86 0.18
In Table I, Eadiab is the minimum voltage required to carry out the
process, assuming 100% current efficiency and that the MgC12 and H2 are fed at
room temperature.
In particular, Table I shows the calculated decomposition voltage
(1000 K) and adiabatic voltage required to cover the energy requirements of
the
process without heat losses.
Table I further shows that the decomposition voltage decreases by 1.04V
and that the overall energy requirement decreases by 0.86V. This means that
with HCI formation, another 0.18V per mole can be dissipated in the cell
without causing overheating. The decrease of 0.86V translates to a reduction
of about 25% less electricity consumption for magnesium production. With
magnesium cells currently requiring an average of 12.5 MW-hr per tonne, and
an average energy cost of 4 cents per KW-hrs, this translates to a savings of
about $125 per tonne of magnesium produced in electrical consumption.
Another major cost saving comes from the fact that the cell is producing
HC1 rather than chlorine, requiring no HC1 synthesis plant. Chlorine treatment
and handling as well as HC1 synthesis can provide for further cost savings.
Environmetal problems associated with chlorine gas production are
expected to be alleviated.
The hydrogen gas may be considered to form a hydrogen anode in the
cell, for discharge of the chloride ions. In such case an anode structure is

CA 02265183 1999-03-11
-5-
provided which, can be of any suitable material, for example, graphite,
silicon
carbide or silicon nitride.

Representative Drawing

Sorry, the representative drawing for patent document number 2265183 was not found.

Administrative Status

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Event History

Description Date
Time Limit for Reversal Expired 2010-03-11
Letter Sent 2009-03-11
Grant by Issuance 2008-01-08
Inactive: Cover page published 2008-01-07
Pre-grant 2007-10-11
Inactive: Final fee received 2007-10-11
Notice of Allowance is Issued 2007-04-25
Letter Sent 2007-04-25
Notice of Allowance is Issued 2007-04-25
Inactive: Approved for allowance (AFA) 2007-03-28
Amendment Received - Voluntary Amendment 2006-12-07
Inactive: S.29 Rules - Examiner requisition 2006-07-07
Inactive: S.30(2) Rules - Examiner requisition 2006-07-07
Inactive: Office letter 2004-02-20
Letter Sent 2004-02-18
Inactive: Single transfer 2004-01-28
Letter Sent 2004-01-19
Letter Sent 2004-01-14
Inactive: Office letter 2004-01-05
Request for Examination Requirements Determined Compliant 2003-12-19
Request for Examination Received 2003-12-19
Reinstatement Requirements Deemed Compliant for All Abandonment Reasons 2003-12-19
All Requirements for Examination Determined Compliant 2003-12-19
Appointment of Agent Requirements Determined Compliant 2003-11-25
Inactive: Office letter 2003-11-25
Inactive: Office letter 2003-11-25
Revocation of Agent Requirements Determined Compliant 2003-11-25
Appointment of Agent Request 2003-11-10
Inactive: Single transfer 2003-11-10
Revocation of Agent Request 2003-11-10
Deemed Abandoned - Failure to Respond to Maintenance Fee Notice 2003-03-11
Application Published (Open to Public Inspection) 2000-09-11
Inactive: Cover page published 2000-09-10
Letter Sent 2000-04-13
Inactive: Single transfer 2000-03-16
Inactive: First IPC assigned 1999-05-11
Inactive: Courtesy letter - Evidence 1999-04-20
Inactive: Filing certificate - No RFE (English) 1999-04-15
Filing Requirements Determined Compliant 1999-04-15
Application Received - Regular National 1999-04-14

Abandonment History

Abandonment Date Reason Reinstatement Date
2003-03-11

Maintenance Fee

The last payment was received on 2007-10-11

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  • the reinstatement fee;
  • the late payment fee; or
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Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
GROUP-CONSEIL GENIVAR INC.
Past Owners on Record
GEZINUS VAN WEERT
Past Owners that do not appear in the "Owners on Record" listing will appear in other documentation within the application.
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Document
Description 
Date
(yyyy-mm-dd) 
Number of pages   Size of Image (KB) 
Description 1999-03-11 5 181
Abstract 1999-03-11 1 14
Claims 1999-03-11 3 81
Cover Page 2000-09-06 1 20
Description 2006-12-07 5 180
Cover Page 2007-11-27 1 25
Filing Certificate (English) 1999-04-15 1 165
Request for evidence or missing transfer 2000-03-14 1 109
Courtesy - Certificate of registration (related document(s)) 2000-04-13 1 113
Reminder of maintenance fee due 2000-11-15 1 112
Courtesy - Abandonment Letter (Maintenance Fee) 2003-04-08 1 178
Reminder - Request for Examination 2003-11-13 1 112
Acknowledgement of Request for Examination 2004-01-19 1 174
Notice of Reinstatement 2004-01-14 1 168
Courtesy - Certificate of registration (related document(s)) 2004-02-18 1 107
Commissioner's Notice - Application Found Allowable 2007-04-25 1 162
Maintenance Fee Notice 2009-04-22 1 171
Maintenance Fee Notice 2009-04-22 1 171
Correspondence 1999-04-20 1 30
Correspondence 2003-11-10 2 75
Correspondence 2003-11-25 1 14
Correspondence 2003-11-25 1 20
Correspondence 2004-01-05 1 27
Fees 2003-12-19 1 27
Correspondence 2004-02-20 1 12
Fees 2005-02-10 1 26
Fees 2006-02-23 1 32
Fees 2006-11-02 1 32
Correspondence 2007-10-11 1 29
Fees 2007-10-11 1 30