The present application is a U.S. National Phase filing of International Application No. PCT/AU2012/001481, filed on Dec. 6, 2012, designating the United States of America and claiming priority to Australian Patent Application No. 2011905072, filed Dec. 6, 20122011, and this application claims priority to and the benefit of the above-identified applications, which are both incorporated by reference herein in their entireties.
The present invention relates to a method of starting a process for smelting a metalliferous material.
The term “metalliferous material” is understood herein to include solid feed material and molten feed material. The term also includes within its scope partially reduced metalliferous material.
The present invention relates particularly, although by no means exclusively, to a method of starting a molten bath-based smelting process for producing molten metal from a metalliferous feed material in a smelting vessel that has a strong bath/slag fountain generated by gas evolution in the molten bath, with the gas evolution being at least partly the result of devolatilisation of carbonaceous material in the molten bath.
In particular, although by no means exclusively, the present invention relates to a method of starting a process for smelting an iron-containing material, such as an iron ore, and producing iron.
The present invention relates particularly, although by no means exclusively, to a method of starting a smelting process in a smelting vessel that includes a main chamber for smelting metalliferous material.
A known molten bath-based smelting process, generally referred to as the HIsmelt process, is described in a considerable number of patents and patent applications in the name of the applicant.
Another molten bath-based smelting process, referred to hereinafter as the “HIsarna” process, is described in International application PCT/AU99/00884 (WO 00/022176) in the name of the applicant.
The HIsmelt process and the HIsarna process are associated particularly with producing molten iron from iron ore or another iron-containing material.
The HIsarna process is carried out in a smelting apparatus that includes (a) a smelting vessel that includes a main smelting chamber and lances for injecting solid feed materials and oxygen-containing gas into the main chamber and is adapted to contain a bath of molten metal and slag and (b) a smelt cyclone for pre-treating a metalliferous feed material that is positioned above and communicates directly with the smelting vessel.
The term “smelt cyclone” is understood herein to mean a vessel that typically defines a vertical cylindrical chamber and is constructed so that feed materials supplied to the chamber move in a path around a vertical central axis of the chamber and can withstand high operating temperatures sufficient to at least partially melt metalliferous feed materials.
In one form of the HIsarna process, carbonaceous feed material (typically coal) and optionally flux (typically calcined limestone) are injected into a molten bath in the main chamber of the smelting vessel. The carbonaceous material is provided as a source of a reductant and a source of energy. Metalliferous feed material, such as iron ore, optionally blended with flux, is injected into and heated and partially melted and partially reduced in the smelt cyclone. This molten, partly reduced metalliferous material flows downwardly from the smelt cyclone into the molten bath in the smelting vessel and is smelted to molten metal in the bath. Hot reaction gases (typically CO, CO2, H2, and H2O) produced in the molten bath is partially combusted by oxygen-containing gas (typically technical-grade oxygen) in an upper part of the main chamber. Heat generated by the post-combustion is transferred to molten droplets in the upper section that fall back into the molten bath to maintain the temperature of the bath. The hot, partially-combusted reaction gases flow upwardly from the main chamber and enter the bottom of the smelt cyclone. Oxygen-containing gas (typically technical-grade oxygen) is injected into the smelt cyclone via tuyeres that are arranged in such a way as to generate a cyclonic swirl pattern in a horizontal plane, i.e. about a vertical central axis of the chamber of the smelt cyclone. This injection of oxygen-containing gas leads to further combustion of smelting vessel gases, resulting in very hot (cyclonic) flames. Finely divided incoming metalliferous feed material is injected pneumatically into these flames via tuyeres in the smelt cyclone, resulting in rapid heating and partial melting accompanied by partial reduction (roughly 10-20% reduction). The reduction is due to both thermal decomposition of hematite and the reducing action of CO/H2 in the reaction gases from the main chamber. The hot, partially melted metalliferous feed material is thrown outwards onto the walls of the smelt cyclone by cyclonic swirl action and, as described above, flows downwardly into the smelting vessel below for smelting in the main chamber of that vessel.
The net effect of the above-described form of the HIsarna process is a two-step countercurrent process. Metalliferous feed material is heated and partially reduced by outgoing reaction gases form the smelting vessel (with oxygen-containing gas addition) and flows downwardly into the smelting vessel and is smelted to molten iron in the smelting vessel. In a general sense, this countercurrent arrangement increases productivity and energy efficiency.
The above description is not to be taken as an admission of the common general knowledge in Australia or elsewhere.
The applicant has proposed that the HIsarna process and an oxygen-blown version of the HIsmelt process be started up in a smelting vessel by feeding hot metal (from an external source) into the main chamber of the vessel via the forehearth of the vessel, commencing supplying oxygen-containing gas (typically technical grade oxygen) and solid carbonaceous material (typically coal) and generating heat in the main chamber. This hot start-up method generates heat via spontaneous ignition of combustible material in the main chamber. The applicant has proposed that this initial step in the hot start-up method be followed by the addition of slag-forming agents and, later on, by the addition of metalliferous feed material (such as ferruginous material such as iron ore) into the main chamber. The hot start method is described in a companion International application entitled “Starting a Smelting Process” lodged in the name of the applicant on the same day as the subject International application for the present invention.
In pilot plant trials of the HIsarna process that were based on technical grade oxygen as the oxygen-containing gas, coal as the solid carbonaceous material, and iron ore fines as the metalliferous material, the above hot start-up method was tested. The applicant found that there is a finite time-window after pouring hot metal into the main chamber of the smelting vessel within which it is possible to safely commence supplying cold oxygen and coal into the main chamber and have spontaneous ignition of combustible material and generate heat in the main chamber which is necessary to start up the process. This time window was found to be typically around 1-2 hours in duration under the pilot plant conditions. The time-window was found to be variable depending on (amongst other factors) smelting vessel geometry, charge metal temperature and charge metal chemistry. It was also found that if the steps of commencing supplying oxygen and coal into the main chamber were not implemented within the requisite time-window, it became impossible to guarantee spontaneous ignition of coal and cold oxygen inside the main chamber. This resulted in a mixture of un-combusted coal and oxygen leaving the main chamber, with a possibility of a coal dust explosion (and associated damage) in downstream equipment.
The applicant has found that the mechanism associated with this time-window is related to the formation of a slag layer on top of the molten metal. Once this slag layer is sufficiently well established, it is cooled by radiation to the smelting vessel, for example to water panels in a top space of the main chamber, and becomes crusty, effectively creating a blanket on the molten metal. The blanket acts as a thermal insulator that restricts heat transfer from the molten metal below the blanket to the top space of the main chamber above the blanket, with a result that the thermal conditions in the top space are too cold to support spontaneous ignition of combustible material in the top space. Whilst not wishing to be bound by the following comment, the applicant believes that this slag formed during the pilot plant trials primarily from (i) residual slag coatings left behind from previous operations and (ii) oxygen reacting with constituents in molten metal (silicon in particular, reacting to form silicon dioxide).
The applicant also found in the pilot plant trials that essentially the same problem occurred if the plant was operating normally and was then stopped (including stopping supplying solid feed materials to the main chamber) for a significant period of time (for example, to perform mechanical repairs outside the smelting vessel). Under these conditions the slag layer is generally significantly thicker compared to the slag layer at start-up of the process. Hot metal is significantly further below the surface of the slag, and is therefore less able to keep the slag upper surface hot by conduction. Surface slag heat was lost to the smelting vessel, for example to water-cooled panels in the top space of the main chamber, by radiation, and a cold, crusty layer formed on the molten bath more rapidly than before. When the smelting vessel was idle for more than about 15-30 minutes, spontaneous ignition of coal and cold oxygen and hence heat generation required to support process start-up in the main chamber of the smelting vessel was once again impossible to guarantee.
During the course of the pilot plant trials the applicant developed a safe, practical method to start the HIsarna process under these conditions. An important basis of the method is recognising the necessity (before cold oxygen and coal or other suitable oxygen-containing gas and solid carbonaceous material can be introduced) to establish a sufficiently large and stable “hot zone” for ignition of oxygen and coal in the main chamber of the smelting vessel by independent means, i.e. independently of and before supplying cold oxygen and coal into the main chamber.
The method of starting a smelting process of the present invention is applicable to starting (which term includes “re-starting”) any molten bath-based smelting process when the thermal conditions (temperatures) inside a top space of the main chamber of the smelting vessel are too cold to allow safe, spontaneous ignition of any newly supplied cold oxygen-containing gas and solid carbonaceous material into the main chamber. As described above, such conditions are typically encountered when a crusty frozen slag layer is present on the upper surface of the molten bath in the main chamber.
According to the present invention there is provided a method of starting a molten-bath based process for smelting a metalliferous feed material to form a molten metal in a smelting apparatus, with the apparatus including a smelting vessel that includes a main chamber that contains a bath of molten metal and there is no injection of solid feed materials into the smelting apparatus at the time of commencing the method, and with the method including the steps of:
The term “cold” in the context of oxygen-containing gas is understood herein to mean cold in the sense that the gas is at a temperature below that required for spontaneous ignition of the carbonaceous material and the oxygen-containing gas mixture (i.e. below about 700-800° C. in the case of a coal-oxygen mixture).
The term “frozen materials” referred in step (c) above includes by way of example a layer of slag, such as the crusty layer of slag found in the pilot plant trials.
The method may include supplying a combustible material to the main chamber prior to step (a) above. By way of example, the method may include supplying a solid combustible material (such as wood, charcoal or other suitable solid material) into the main chamber by manually inserting the combustible material through an opening (such as the slag notch) in the main chamber. By way of further example, the method may include supplying a gaseous combustible material or a liquid combustible material into the main chamber. The gaseous combustible material may be natural gas. The liquid combustible material may be oil.
This optional step of feeding the combustible material into the main chamber prior to step (a) may not be required in situations where the crusty layer is thin and/or not fully formed and there may be sufficient combustible material already in the main chamber to support combustion via the ignition source when oxygen-containing gas supply is commenced in step (b). In some situations, for example when the method is used after a short interruption to a smelting campaign, the crusty layer may not be fully established and there may be sufficient residual combustible material in the vessel to support ignition when oxygen-containing gas supply is commenced in step (b). In other situations, the method may include supplying a combustible material to the main chamber after step (a) of inserting the external ignition source into the main chamber and prior to step (b) of commencing supplying the cold oxygen-containing gas into the main chamber and igniting combustible material in the main chamber. The combustible material may be a solid or a gaseous or a liquid combustible material as described above.
In general, the above options of supplying a combustible material to the vessel prior to or after inserting the external ignition source into the main chamber may be used at different times. If a plant stoppage is relatively short (but too long to simply commence supplying coal and oxygen or other suitable carbonaceous material and oxygen-containing gas without providing an ignition source), then the addition of combustible material into the main chamber prior to step (b) may not be necessary. For longer stoppages the other options involving supplying the combustible material into the main chamber prior to or after step (a) may be required.
The method may include (under start-up conditions or when a slag inventory in the main chamber is low) commencing supplying slag or slag forming materials to the main chamber to form a slag on the molten metal after step (c) and before step (d) above.
The ignition source for step (a) of inserting the external ignition source into the main chamber may be adapted to operate for a time-duration of at least 3 minutes, typically at least 5 minutes.
The ignition source for step (a) may be selected on the basis that it does not require gaseous oxygen in the main chamber in order to stay alight.
The ignition source for step (a) may carry its own “on-board” oxygen (e.g. in the form of iron oxide) such that it burns regardless of whether it is in air, oxygen or nitrogen. With regard to the reference to nitrogen, it is noted that nitrogen (or some other inert gas) purge of solids injection lances will generally be used and, at this point in the method, there may be little if any gaseous oxygen available inside the main chamber.
The ignition source for step (a) may be a magnesium-based flare.
The method may include verifying that the external ignition source is alight in the main chamber after inserting the external ignition source into the main chamber in step (a).
The step of verifying that the ignition source is alight in the main chamber may be via direct observation or via a camera mounted within a suitable opening such as a slag notch in the smelting vessel.
Step (b) of commencing supplying the cold oxygen-containing gas and igniting combustible material in the main chamber may include commencing supplying oxygen into the main chamber and igniting combustible material in the main chamber.
Step (b) of commencing supplying the cold oxygen-containing gas and igniting combustible material in the main chamber may include commencing supplying technical grade oxygen at a feed temperature below 800° C. into the main chamber and igniting combustible material in the main chamber.
Step (b) of commencing supplying the cold oxygen-containing gas and igniting combustible material in the main chamber may include commencing supplying a small amount of cold oxygen (typically 10-30% of normal oxygen flow for the process) to the main chamber. In such a situation, combustible material present in the main chamber (such as residual carbonaceous material from an earlier operation and/or wood as the optional combustible material supplied to the main chamber prior to step (a)) should ignite and burn.
The method may include verifying ignition of combustible material after step (b) of igniting combustible material in the main chamber.
The step of verifying ignition may be via direct observation or via a suitable camera that material is burning in the main chamber. The use of wood as the optional combustible material supplied to the main chamber prior to step (a) is particularly advantageous since it will burn for several minutes with a bright, easy-to-recognise flame.
Step (c) of commencing supplying the carbonaceous material into the main chamber may include supplying the carbonaceous material at a feed temperature below 150° C. The carbonaceous material may be a solid material (such as coal) or a gaseous material (such as natural gas) or a liquid material (such as oil).
Step (c) may include verifying that carbon dioxide generation in the main chamber is ongoing via an on-line gas analysis system.
Step (d) may include ramping up supplying the oxygen-containing gas and the carbonaceous material supplied in earlier steps of the method or supplying increasing amounts of other oxygen-containing gas and carbonaceous material into the main chamber. By way of example, it may be preferable to use gaseous carbonaceous material in step (c) of the method and to switch over to supplying a solid carbonaceous material when the metalliferous material is supplied to the main chamber in step (d).
Step (d) may include ramping up supplying the metalliferous material into the main chamber.
The apparatus may include (i) the above-described smelting vessel that is adapted to contain a bath of molten metal and (ii) a smelt cyclone that is positioned above and communicates with the smelting vessel. In that event, step (d) may include commencing supplying the metalliferous feed material and the oxygen-containing gas into the smelt cyclone and generating a horizontally rotating flow of material in the cyclone and combusting combustible gas flowing upwardly into the cyclone from the vessel and partially reducing and melting the metalliferous feed material in the cyclone, whereby the partially reduced molten metalliferous feed material flows downwardly from the cyclone into the molten bath of metal and slag in the main chamber of the smelting vessel and is smelted to molten metal in the bath.
The method of present invention is applicable to a molten bath-based smelting apparatus that includes (a) a smelting vessel that has a main chamber that is adapted to contain the bath of molten metal and slag, (b) lances or other suitable means for supplying the carbonaceous material into the bath, (c) lances or other suitable means for supplying the oxygen-containing gas into the bath (d) lances or other suitable means for supplying the metalliferous material to the bath, either directly or via a smelt cyclone, (e) a means such as a forehearth for removing metal and slag from the main chamber, and (f) at least 40%, typically at least 50%, of the wall region of the smelting vessel above the bath being covered by water-cooled panels with frozen slag layers.
Under normal operating conditions, the molten bath-based smelting process includes the steps of:
The oxygen-containing gas may be air, oxygen, or oxygen-enriched air.
An embodiment of a method of starting a smelting process in a smelting vessel in accordance with the present invention is described with reference to the accompanying drawings, of which:
The HIsarna process smelts metalliferous feed material and produces process outputs of molten metal, molten slag, and an off-gas. The following description of the HIsarna process is in the context of smelting metalliferous material in the form of iron ore. The present invention is not limited to this type of metalliferous material.
The HIsarna apparatus shown in
With reference to
Normal operation of the HIsarna process during a smelting campaign involves (a) coal injection via lances 35 and cold oxygen injection via lances 37 into the main chamber 19 of the smelting vessel 4 and (b) ore injection 7 and additional oxygen injection 8 into the smelt cyclone 2.
The operating conditions, including but not limited to, coal and oxygen feed rates into the main chamber 19 of the smelting vessel 4 and ore and oxygen feed rates into the smelt cyclone 2 and heat losses from the main chamber 19, are selected so that offgas leaving the smelt cyclone 2 via an offgas outlet duct 9 has a post-combustion degree of at least 90%.
Offgas from the smelt cyclone 2 passes via an offgas duct 9 to an offgas incinerator 10, where additional oxygen 11 is injected to burn residual CO/H2 and provide a degree of free oxygen (typically 1-2%) in the fully combusted flue gas.
Fully combusted offgas then passes through a waste heat recovery section 12 where the gas is cooled and steam is generated. Flue gas then passes through a wet scrubber 13 where cooling and dust removal are achieved. The resulting sludge 14 is available for recycle to the smelter via the ore feed stream 1.
Cool flue gas leaving the scrubber 13 is fed to a flue gas desulphurisation unit 15.
Clean flue gas is then vented via a stack 16. This gas consists mainly of CO2 and, if appropriate, it can be compressed and geo-sequestered (with appropriate removal of residual non-condensable gas species).
With particular reference to the enlarged cross-sectional view of the smelting vessel 4 shown in
With further reference to
In accordance with one embodiment of the method of the present invention, in order to safely start the HIsarna process in this “idle” state, the following steps are taken:
The above description focuses on starting the HIsarna process after there has been a process interruption of at least 15-30 minutes during which a crusty slag layer 29 forms on the molten bath in the main chamber 19. The same method steps 1-7 to start the HIsarna process set out above can be used during an initial start-up process for the HIsarna process in a situation where a crusty layer 29 forms during the course of that start-up process.
Many modifications may be made to the embodiment of the process of the present invention described above without departing from the spirit and scope of the invention.
By way of example, step 1 is not confined to the use of solid combustible material, and gaseous or liquid combustible materials may also be used.
By way of further example, the present invention is not limited to the addition of combustible material prior to inserting the ignition source into the smelting vessel 4. Specifically, there may be situations where it is preferable to add combustible material after inserting the ignition source into the vessel and before commencing supply of cold oxygen (or other suitable oxygen-containing gas). In some situations, the addition of combustible material may not be required at all and ignition can be achieved on the basis of residual combustible material in the smelting vessel 4.
By way of further example, visual (or other) observation that the ignition source is alight may not be necessary in step 2 in situations where the ignition source has its own source of oxygen.
By way of further example, the present invention is not confined to the time duration of at least 15-30 minutes during which there is no supply of solid feed materials into the smelt cyclone 2 and the smelting vessel 4. The time period may vary depending on a range of factors including the type of metalliferous material and the characteristics of the smelting vessel, such as the rate of heat loss from slag to the vessel. In any given situation, the time period is the time required for crusty slag to form on the molten bath to an extent that it is problematic to start injection of cold oxygen and coal to the main chamber 19 of the smelting vessel 4.
The above description focuses on coal as the carbonaceous material and technical grade oxygen for the oxygen-containing gas. The present invention is not so limited and extends to any suitable oxygen-containing gas and any suitable solid carbonaceous materials.
The above-described embodiment focuses on the HIsarna process. The present invention is not limited to the HIsarna process and extends to any molten bath-based process in a smelting vessel. By way of example, the present invention extends to the oxygen-blown version of the HIsmelt process. As is indicated above, the HIsmelt process is described in a considerable number of patents and patent applications in the name of the applicant. By way of example, the HIsmelt process is described in International application PCT/AU96/00197 in the name of the applicant. The disclosure in the patent specification lodged with the International application is incorporated herein by cross-reference.
Number | Date | Country | Kind |
---|---|---|---|
2011905072 | Dec 2011 | AU | national |
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/AU2012/001481 | 12/6/2012 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2013/082653 | 6/13/2013 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
6517605 | Bates et al. | Feb 2003 | B1 |
8366992 | Williams | Feb 2013 | B2 |
20080295647 | Kwon | Dec 2008 | A1 |
20090031858 | Farr | Feb 2009 | A1 |
20100011908 | Goodman | Jan 2010 | A1 |
Number | Date | Country |
---|---|---|
0022176 | Apr 2000 | WO |
2006119575 | Nov 2006 | WO |
Entry |
---|
International Search Report mailed Feb. 11, 2013 (PCT/AU2012/001481); ISA/AU. |
Written Opinion mailed Feb. 11, 2013 (PCT/AU2012/001481); ISA/AU. |
Australian Patent Office International-Type Search Report mailed Apr. 2, 2012 (PCT/AU2012/001481); ISA/AU. |
Number | Date | Country | |
---|---|---|---|
20140318319 A1 | Oct 2014 | US |