Mixed Rare Earth Carbonate and Titanium Products from Anatase-Bearing Feed at the Tiros Project

Figure 17.6 Process Flow Diagram REE Recovery, Fine circuit

The Tiros Rare Earths and Titanium Project is a preliminary economic assessment stage project located in Minas Gerais, Brazil, owned by Resouro Strategic Metals Inc. The project targets rare earth elements and titanium from anatase-bearing feed material. Construction timing is not stated in the source material.

Critical Data

Parameter Value Unit Notes
Plant feed 500,000 t/a ROM mineralized material
Feed TiO₂ grade 26.3 % Average
Feed Fe₂O₃ grade 31.95 % Average
Feed Al₂O₃ grade 11.47 % Average
Feed SiO₂ grade 22.95 % Average
Feed TREO grade 10,852 ppm Average
Operating days 365 d/a Design value
Operating availability 92 % Design value
Operating hours per year 8,059 h/a At stated availability
Fine TiO₂ product 47,865 t/a Design value
Coarse TiO₂ product 42,390 t/a Design value
Global TiO₂ recovery 68.7 % Design value
Feed TREO 5,426 t/a Design value
TREO recovered in MREC 3,636 t/a Approximate design value
Global TREO recovery 67.0 % Design value
MREC production rate Not stated t/a To be confirmed
MREC TREO grade Not stated % To be confirmed
Total raw water requirement 391 m³/h Projected design value
Coarse area water consumption 130 m³/h Design value
Fine area water consumption 54.5 m³/h Design value
Reagents water consumption 154 m³/h Design value
Cooling water make-up 1.89 m³/h Design value
Other water consumption 50.7 m³/h Design value
LIMS field strength (coarse circuit, first stage) 1,000 Gauss Design value
LIMS field strength (coarse circuit, second stage) 2,000 G Design value
LIMS field strength (fines circuit) 800 Gauss Design value
Calcination temperature 600 °C Design value
Calcination residence time 60 minutes Design value
Post-kiln air cooling target 100 °C Design value
Post-kiln water cooling target 50 °C Design value
Acid baking temperature 300 °C Design value
Acid baking residence time ~1 hour Design value
HCl leaching temperature 90–100 °C Design value
HCl leaching time ~90 minutes Design value
HCl leach solution concentration ~16 wt% Design value
HCl consumption 0.056 t/t ROM Active HCl; design value
HCl consumption as 34% solution 0.164 t/t ROM Design value
Coarse area HCl consumption 82,192 t/a Design value
Coarse area CO consumption 685 t/a Design value
Fine area Mg(OH)₂ (95%) consumption 2,397 t/a Design value
Fine area Na₂CO₃ (95%) consumption 3,725 t/a Design value
Fine area CO consumption 10,205 t/a Design value
Fine area H₂SO₄ (96%) consumption 186,986 t/a Design value
Fine area NaOH (98%) consumption 102,534 t/a Design value

Overview

The Tiros deposit is shallow, soft, and highly weathered. That makes the material friable and easy to handle. Conventional crushing and milling equipment for hard rock is not required. The flowsheet relies on disaggregation and size classification.

The processing plant is designed to produce upgraded titanium products and a Mixed Rare Earth Carbonate. Two main circuits are used. The coarse circuit handles material between 75 µm and 300 µm and produces an upgraded anatase concentrate. The fines circuit handles material below 75 µm and produces a fine titanium product plus an MREC.

Key Process Stages

The ROM mineralized material is trucked to the plant and fed into a scrubber inlet screen for initial separation. The scrubber is a trommel scrubber. It is a rotating cylindrical drum with an internal washing and disaggregation section and a perforated screening section at the discharge end. Agglomerates and clay crusts break down inside the drum. Process water is fed at high pressure to disperse clays and detach fine TiO₂ and REE particles from coarser fragments. Material that meets the required particle size passes through the perforations as slurry. Oversized lumps discharge to the tailings area.

Disaggregated material goes to a screen with a 300 µm cut size. Material over 300 µm goes to a rod mill. The rod mill has a perforated screening section at the discharge end that separates material smaller than 300 µm. Undersize recirculates to the screen. Oversized lumps go to tailings.

Material under 300 µm goes to a second screen with a 75 µm cut size. Material between 75 µm and 300 µm goes to the coarse circuit. Material below 75 µm goes to the fines circuit for REE recovery.

In the coarse circuit, the 75–300 µm material is fed to a low intensity magnetic separator operating at 1,000 Gauss. Process water is added. Iron content drops from 42.3% to 17.4% in the non-magnetic fraction. The magnetic fraction goes to a thickener and filter. Overflow from the thickener goes to water treatment. Filtrate returns to the thickener. Wet solid goes to tailings.

The non-magnetic fraction goes to a gravimetric separation unit. Silicon content drops from 16.0% to 4.5% SiO₂ in the heavy fraction. The light fraction is high in kaolinite and quartz and goes to a thickener and filter.

The heavy fraction goes to a thickener and filter for solid–liquid separation. Overflow goes to water treatment. Filtrate returns to the thickener.

The filter cake goes to a rotary kiln. The upstream section dries and preheats the material. Calcination takes place at 600°C for 60 minutes under a controlled atmosphere. Carbon monoxide is used as the reducing agent. It is generated externally in a dedicated unit and introduced as a CO-rich gas stream. Iron reduces from Fe³⁺ to Fe²⁺, increasing magnetic susceptibility. Off gases go through a dedicated gas handling and treatment system.

The discharge from the rotary kiln is at approximately 600°C. An air-cooling unit reduces the temperature to approximately 100°C. A water-cooling stage further reduces it to around 50°C.

The cooled material goes to a LIMS operating at approximately 2,000 G. This removes residual iron-bearing minerals. Iron content in the non-magnetic product drops to approximately 5% Fe. The magnetic fraction goes to the tailings storage facility.

The non-magnetic fraction goes to electrostatic separation. This exploits differences in electrical conductivity. Feed material must be dry. Conductive and non-conductive particles follow different trajectories. Silicon-containing minerals are recovered in the non-conductor fraction and go to tailings. Anatase reports to the conductor fraction. SiO₂ in the conductor material drops to less than 1.0%.

The conductive fraction undergoes hydrochloric acid leaching at 90–100°C for approximately 90 minutes. The leach solution contains approximately 16 wt% HCl. Hydrochloric acid consumption is approximately 0.056 tonne of active HCl per tonne of ROM. That is equivalent to 0.164 tonne of 34% HCl solution as supplied per tonne of ROM. The upgraded anatase concentrate has an anticipated TiO₂ grade exceeding 80%. This is the proposed coarse titanium product. Its suitability for conventional pigment production and chlorination performance remain to be confirmed.

In the fines circuit, material passing 75 µm goes to a LIMS operating at 800 Gauss. The magnetic fraction is mostly iron and goes to a thickener and filter for tailings disposal and liquid recovery.

The non-magnetic fraction goes to a rotary kiln. The material is dried and preheated in the initial section. Discharge is at approximately 600°C. Air cooling reduces it to approximately 100°C. Water cooling reduces it to 50°C. The material then goes to a dry magnetic separator. The magnetic fraction goes to tailings.

The non-magnetic fraction goes to an acid baking rotary kiln. Concentrated sulfuric acid is mixed with the material to form a reactive paste. Thermal treatment is at 300°C for approximately one hour. REE are converted to soluble sulfates. Fe, Al, and Ti also react. An acid-regeneration unit has been assumed in the process design. It is proposed to operate at approximately 600°C. Acid regeneration is a conceptual and untested design assumption at the PEA stage.

The calcine is cooled and transferred to agitated leaching reactors. Sequential washing with water dissolves the REE sulfates along with Fe, Al, and Ti sulfates. Non-converted minerals, primarily SiO₂, remain undissolved. Solid–liquid separation in a filter produces a clarified liquor and a low-moisture solid residue that goes to tailings.

A subsequent stage is proposed for titanium removal. The clarified sulfate liquor undergoes controlled neutralization using 10 wt% NaOH in agitated reactors. Hydrated titanium oxide precipitates. Titanium-bearing solids are recovered by filtration. This step has not been demonstrated for the Tiros process liquor. Sodium–rare earth double sulfates may precipitate and cause REE losses. Future testwork should confirm titanium-removal selectivity.

The REE-bearing liquor goes through purification. Mg(OH)₂ is added in impurity removal agitated reactors. In the first reactor, Mg(OH)₂ increases pH and promotes precipitation of iron and aluminum. Further Mg(OH)₂ addition adjusts pH for precipitation of potassium, calcium, and other ions. REE remain in solution. Filtration produces a clarified liquor and a low-moisture filter cake for disposal.

The purified REE liquor goes to precipitation agitated reactors. A sodium carbonate solution is added under controlled pH and temperature. MREC precipitates. The slurry is filtered. The solid MREC goes to a reslurry tank for washing to reduce residual impurities. The washed slurry is dewatered in a filter press. The MREC product is suitable for downstream separation and refining.

The total projected raw water requirement is approximately 391 m³/h. Water will be sourced from local catchments. It supplies process water, demineralized water, and cooling water make-up. Demineralized water is used for reagent preparation and acid dilution. A water treatment plant is planned to process liquid streams from solid–liquid separation stages for conditioning and reuse. The design of the Water Recovery System will be undertaken in the next study phase.

Carbon monoxide for both circuits is produced from charcoal through combustion and calcination. Hydrochloric acid is delivered in tanker trucks and diluted to 16% with process water. Sulfuric acid is received at 96% concentration. Sodium hydroxide is received as bagged solid and dissolved to a 10% solution. Magnesium hydroxide is received as bagged solid and prepared as a 10 wt% slurry. Sodium carbonate solution is prepared at 25% w/w. Diesel is used for backup electricity generation. LPG is used for kiln equipment.

Additional Interesting Data and Summary

The process design criteria were developed on a preliminary PEA basis. The mass balance is based on laboratory testwork by Resouro along with preliminary design assumptions and benchmarks from analogous operations. Process conditions should be considered preliminary.

At the stated plant throughput and feed grade, the feed contains approximately 5,426 t/a TREO. Of that, approximately 3,636 t/a TREO is estimated to report to the MREC. The MREC production rate, composition, and TREO grade remain subject to confirmation.

The LIMS in the coarse circuit reduces iron content from 42.3% to 17.4% in the non-magnetic fraction. The gravimetric separation lowers silicon content from 16.0% to 4.5% SiO₂ in the heavy fraction. After the second LIMS, iron content in the non-magnetic product is approximately 5% Fe. Electrostatic separation reduces SiO₂ to less than 1.0% in the conductor material. The final anatase concentrate is anticipated to exceed 80% TiO₂.

Key Processes

  • Scrubbing and size classification for feed preparation
  • Low intensity magnetic separation for iron removal
  • Gravimetric separation for silicon removal
  • Reductive calcination with carbon monoxide
  • Dry magnetic separation after calcination
  • Electrostatic separation for final silica rejection
  • Hydrochloric acid leaching for anatase upgrading
  • Acid baking with sulfuric acid for REE conversion
  • Water leaching of calcine
  • Selective precipitation of titanium using sodium hydroxide
  • Impurity removal with magnesium hydroxide
  • MREC precipitation with sodium carbonate
  • Solid–liquid separation at multiple stages throughout the flowsheet

Source: NI 43-101 Technical Report and Preliminary Economic Assessment for the Tiros Rare Earths and Titanium Project, Minas Gerais, Brazil, July 10, 2026. Project website: Tiros Rare Earths and Titanium Project

Consolidated report summaries

The following former standalone pages about this operation were consolidated here in October 2026. They are retained for source traceability; dates and figures reflect each report’s own effective date and may be superseded by the current information above.

Tiros Process Design Centers on HCl Leach and Sulfuric Acid Bake Routes

A look at the process design in the preliminary economic assessment for Resouro Strategic Metals' Tiros rare earths and titanium project in Brazil, covering the two main processing routes for coarse and fine material.

The Tiros Rare Earths and Titanium Project is an advanced project located in Minas Gerais, Brazil, roughly at latitude -19.05° South and longitude -45.934° West. The project is owned by Resouro Strategic Metals Inc. and is focused on producing upgraded titanium products from anatase-bearing feed, along with a Mixed Rare Earth Carbonate (MREC). The proposed process recovers titanium into fine and coarse product streams, while rare earth elements are captured in the MREC. At the current preliminary economic assessment stage, the product specifications and market suitability remain subject to confirmation through further testwork and product qualification.

Critical Data

Parameter Value Unit Notes
Plant feed 500,000 t/a Nominal processing capacity
TiO₂ feed grade 26.3 % Average feed grade; Table 17.2 lists 26.3% while text states 26.27%
TREO feed grade 10,852 ppm Average feed grade
Operating days 365 d/a
Operating availability 92 %
Operating hours 8,059 h/a At 92% availability
TiO₂ fine product 47,865 t/a
TiO₂ coarse product 42,390 t/a
Global TiO₂ recovery 68.7 %
TREO in feed 5,426 t/a
TREO recovered in MREC 3,636 t/a Approximate
Global TREO recovery 67.0 %
Raw water requirement 391 m³/h Total projected
HCl consumption, coarse area 82,192 t/a
CO consumption, coarse area 685 t/a
H₂SO₄ consumption, fine area 186,986 t/a Received at 96% concentration
NaOH consumption, fine area 102,534 t/a Received as bagged solid (98%)
Na₂CO₃ consumption, fine area 3,725 t/a Received as soda ash (95%)
Mg(OH)₂ consumption, fine area 2,397 t/a Received as bagged solid (95%)
CO consumption, fine area 10,205 t/a
MREC production rate Not stated t/a Subject to confirmation
TREO grade in MREC Not stated % To be confirmed

Overview

The Tiros processing flowsheet takes advantage of the deposit's shallow, soft, and highly weathered mineralization. Because the material is friable, conventional crushing and milling equipment used for hard rock is not needed. The design instead relies on disaggregation and size classification to prepare the feed for the downstream beneficiation stages.

Run of mine material arrives by truck and enters a Scrubber Inlet Screen for a first separation. It then moves to a trommel scrubber, which is a rotating cylindrical drum with an internal washing and disaggregation section followed by a perforated screening section at the discharge end. High-pressure process water disperses clays and detaches fine TiO₂ and REE particles from coarser fragments. Material that meets the size requirement passes through the perforations as slurry, while oversized lumps continue to the end of the drum and go to tailings.

The disaggregated slurry is pumped to a screen with a cut size of 300 µm. This produces two streams. Material over 300 µm goes to a Rod Mill to reduce particle size and liberate target minerals. The mill discharge has a perforated screening section that separates material smaller than 300 µm. That undersize is recirculated to the screen for subsequent processing, and oversized lumps go to tailings disposal.

Material under 300 µm continues to a screen with a cut size of 75 µm. The fraction between 75 µm and 300 µm goes to the coarse circuit and becomes the titanium product stream. Material below 75 µm is routed to the REE recovery circuit, which handles the fine titanium and rare earth elements processing stream.

Key Process Stages

Coarse Circuit Titanium Dioxide Route. The coarse circuit uses an HCl-based approach to selectively remove impurities from the titanium-bearing minerals. The feed material in the 75 µm to 300 µm range enters a Low Intensity Magnetic Separation unit operating at 1,000 Gauss. This stage reduces iron content from 42.3% to 17.4% in the non-magnetic fraction. The magnetic fraction goes to a thickener and filter, with the wet solid sent to tailings.

The non-magnetic fraction proceeds to gravimetric separation, where particles are separated by specific gravity. This lowers silicon content from 16.0% to 4.5% SiO₂ in the heavy fraction. The light fraction, rich in kaolinite and quartz, goes to a thickener and filter. The heavy fraction with high anatase content goes through solid-liquid separation before entering a rotary kiln.

The rotary kiln operates at 600°C with a residence time of 60 minutes under a controlled atmosphere. Carbon monoxide, generated externally from charcoal combustion, is introduced as a gas stream to reduce iron from Fe³⁺ to Fe²⁺. This increases the magnetic susceptibility of the iron-bearing phases. The discharge from the kiln cools through an air-cooling unit to about 100°C, then a water-cooling stage brings it down to around 50°C.

The cooled material enters a second LIMS operating at approximately 2,000 Gauss. This removes residual iron-bearing minerals and reduces iron content to about 5% Fe in the non-magnetic product. The magnetic fraction goes to tailings.

Electrostatic separation follows to further reduce silica. The feed must be dry because moisture affects electrical conductivity and separator performance. Anatase reports to the conductor fraction, and silica-bearing minerals go to the non-conductor fraction and then tailings. This stage reduces SiO₂ to less than 1.0% in the conductor material.

The conductive fraction undergoes hydrochloric acid leaching at 90 to 100°C for about 90 minutes. The leach solution contains approximately 16 wt% HCl. Consumption is about 0.056 tonnes of active HCl per tonne of ROM, equivalent to 0.164 tonnes of 34% HCl solution per tonne of ROM. The anatase-rich product reaches an anticipated TiO₂ grade exceeding 80% and is proposed as the final coarse titanium product.

Fines Circuit Fine Titanium Dioxide and MREC Route. Material passing 75 µm enters the REE recovery circuit. It first goes through a LIMS operating at 800 Gauss to remove metallic minerals, particularly iron-bearing phases. The magnetic fraction goes to a thickener and filter for tailings disposal.

The non-magnetic fraction enters a rotary kiln for drying and preheating. The kiln discharge at approximately 600°C cools through an air-cooling unit to about 100°C, then a water-cooling unit brings it to around 50°C. This cooled material goes through a dry magnetic separator, with the magnetic fraction sent to tailings.

Acid baking follows in a rotary kiln using concentrated sulfuric acid. The material mixes with H₂SO₄ to form a reactive paste and undergoes thermal treatment at 300°C for about one hour. This decomposes the mineral structure and converts REE to soluble sulfates. Iron, aluminum, and titanium also react, increasing acid consumption.

An acid-regeneration unit is assumed in the process design to reduce net acid consumption. The unit operates at approximately 600°C and produces an SO₃-bearing gas that gets captured and hydrated to regenerate concentrated H₂SO₄ for recycling. This is a conceptual and untested assumption at the PEA stage and requires validation in the next study phase.

The calcine from the baking stage cools through air and water coolers before going to agitated leaching reactors. Sequential washing with water dissolves the converted REE sulfates along with iron, aluminum, and titanium sulfates. Non-converted minerals, primarily SiO₂, remain undissolved and are removed by solid-liquid separation. The clarified liquor moves on, and the low-moisture solid residue goes to tailings.

Purification and REE Carbonation. Titanium removal from the clarified sulfate liquor uses controlled neutralization with 10 wt% NaOH in agitated reactors. This promotes hydrolysis and precipitation of hydrated titanium oxide. The titanium-bearing solids are recovered by filtration. The source notes this step has not been demonstrated for the Tiros process liquor, and sodium-rare earth double sulfates may precipitate and cause REE losses to the titanium-bearing solids.

Impurity removal uses controlled addition of Mg(OH)₂ in agitated reactors. The first reactor increases pH to promote precipitation of iron and aluminum. Subsequent additions adjust pH to favor precipitation of potassium, calcium, and other ions while keeping the rare earth elements in solution. Filtration produces a clarified liquor and a low-moisture filter cake for tailings.

The purified REE liquor goes to precipitation reactors where a sodium carbonate solution is added under controlled pH and temperature. This precipitates a Mixed Rare Earth Carbonate. The slurry goes through a filter, and the solid MREC transfers to a reslurry tank for washing to reduce residual impurities. A filter press dewaters the washed slurry, producing the MREC product.

Additional Interesting Data and Summary

The process design criteria are preliminary and based on a nominal capacity of 500,000 t/a. The average feed grades are 26.27% TiO₂ and 10,852 ppm TREO, though Table 17.2 lists 26.3% TiO₂. The mass balance comes from laboratory testwork by Resouro plus preliminary design assumptions and benchmarks from analogous operations.

Global recoveries of 68.7% for TiO₂ and 67.0% for TREO are adopted for producing the fine and coarse titanium products and an MREC. At the stated throughput and feed grade, the feed contains roughly 5,426 t/a TREO, with about 3,636 t/a estimated to report to the MREC. The MREC production rate, composition, and TREO grade remain subject to confirmation.

Water requirements total approximately 391 m³/h. The breakdown by area is 130 m³/h for the coarse area, 54.5 m³/h for the fine area, 154 m³/h for reagents, 1.89 m³/h for cooling water makeup, and 50.7 m³/h for others. Water comes from local catchments and supplies process water, demineralized water, and cooling water makeup. Demineralized water is used for reagent preparation and acid dilution to minimize dissolved contaminants.

A water treatment plant is considered to process liquid streams from the solid-liquid separation stages. These streams contain dissolved solids and must be treated before reuse. The design and development of the Water Recovery System will happen in the next PFS phase.

Air supply covers instrument and equipment needs through compressors, dryers, and filters distributed to plant areas. Cooling air uses forced-air equipment sized for projected thermal loads. Diesel is stored for backup electricity generation. LPG is stored and distributed for kiln equipment. A portion of freshwater from the local river goes to a fire system tank for emergency response.

Key Processes

  • Scrubbing and size classification for feed preparation
  • Rod mill for coarse material size reduction and mineral liberation
  • Low intensity magnetic separation at various gauss levels for iron removal
  • Gravimetric separation for silica reduction
  • Rotary kiln calcination and reductive roasting at 600°C
  • Electrostatic separation for silica removal
  • Hydrochloric acid leaching for anatase purification
  • Sulfuric acid baking at 300°C for REE conversion
  • Water leaching of calcine to dissolve REE sulfates
  • Selective neutralization for titanium, iron, and aluminum removal
  • Sodium carbonate precipitation to produce MREC

Source: NI 43-101 Technical Report and Preliminary Economic Assessment for the Tiros Rare Earths and Titanium Project, July 28, 2026. Project website: Tiros Rare Earths and Titanium Project

Mineral processing basics

Scroll to Top