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Comparison of the immature profile of the laterites from the Izabal Geosol with wet and dry laterites. 

Comparison of the immature profile of the laterites from the Izabal Geosol with wet and dry laterites. 

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Chesbar Resources Inc.1 is developing a nickel-cobalt laterite project in Guatemala, Central America, by applying existing atmospheric chloride technology to a known resource. The tropical laterite project has an inferred resource of 133 million tonnes grading 1.51% nickel, which represents ∼20% of Chesbar's land holdings in Guatemala. Within its b...

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... Resources Inc. is developing a nickel-cobalt laterite project in Guatemala, Central America, by applying existing atmospheric chloride technology to a known resource. The tropical laterite project has an inferred resource of 133 million tonnes grading 1.51% nickel, which represents ~20% of Chesbar’s land holdings in Guatemala. Within its boundaries, the Sechol area has a measured resource of 14 million tonnes grading 1.46 % nickel and 0.08% cobalt, and an indicated resource of 23 million tonnes grading 1.34% nickel and 0.08% cobalt. Notwithstanding the impressive overall resource, the company has taken an innovative approach to a laterite project and is concentrating on El Inicio, a high-grade starter pit with five million tonnes grading 2.1% nickel and 0.08 % cobalt. The process flowsheet is based on atmospheric chloride leaching in a slightly acidic magnesium chloride brine, solution purification by recycled magnesia, precipitation of a mixed nickel/cobalt hydroxide intermediate product, and lixiviant regeneration by modified pyrohydrolysis technology. Initial results suggest that >90% of the contained nickel and cobalt in the non-magnetic fraction of the feed can be recovered, with <5% of the iron leaching. A metallurgical scoping study has established preliminary capital and operating costs for a production facility at a proposed rate of 20,000 tonnes per year of nickel as the intermediate mixed hydroxide. A preliminary assessment of producing a magnesium oxide by-product has also been carried out. This paper reports on the current development of the project and highlights the advantages of working in a chloride medium at atmospheric pressure and slightly elevated temperatures. Chesbar Resources is a Canadian Exploration Company, formed in the 1930s and listed on the Toronto Stock Exchange, Canada. A joint venture agreement between Intrepid Minerals Corporation and Chesbar (75/25), known as Minera Mayamerica S.A., was originally signed in January, 1998 with the objective of exploring for gold and silver; prior to that, Chesbar had been involved in gold exploration in Venezuela. In December, 1998, Minera Mayamerica S.A. was granted the original nickel licences in Guatemala for properties adjacent to Inco’s Exmibal deposit, and in 2001, Chesbar subsequently acquired 100% of Mayamerica with the objective of establishing a nickel/cobalt production facility. A more detailed description of the geology of the Guatemalan Laterite Belt has been given in a previous publication [1]. The Sechol group of deposits comprises several large lateritic pockets, which are delimited by tectonic faults and hosted by ultramafic rocks, mainly dunites and pyroxenites, and usually strongly serpentinized. As a result of the study of several laterite profiles in the area, and using the definitions established by the North American Stratigraphic Code, a new pedostratigraphic unit was defined, The Izabal Geosol, which is composed of five pedological horizons: 3⁄4 Gossan or Iron Hat (not always present) 3⁄4 Limonitic Horizon 3⁄4 Stone Line 3⁄4 Mottled Zone Horizon (also known as the Transition Zone) 3⁄4 Saprolite Horizon. The saprolite horizon marks the bottom part of the Izabal Geosol, and lies directly over the saprock horizon which continues into the less weathered bedrock. The most complete profiles are usually present over weathered dunites and serpentinites, while on top of the less altered pyroxenites, there is usually the formation of only a limonitic zone. All of the laterite deposits in Guatemala are associated with an ophiolitic belt that probably intruded during the Tertiary Era. The young age and the petrologic composition of these ultramafic rocks, together with the climatic conditions of the area, are responsible for the formation of these immature profiles, shown in Figure 1. The extensive regional position held by Chesbar Resources Inc. within the Guatemalan Ophiolitic Belt provides the potential for similar or even larger-scale deposits than the Sechol Group which have already been identified. The 2002 exploration program identified several potential deposits within the Sechol property and in other adjacent licences. Including the work completed in the Marichaj, San Lucas and Sechol properties, Chesbar has already identified resources of 133 M tonnes grading 1.51% Ni and 0.08% Co. Currently, the company has a total of 15 claims, representing 741 km 2 of potential lateritic targets, as shown in Figure 2. In accordance with the Canadian NI 43-101 legislation, Chesbar has identified the following resources (Table I) in the Sechol Property, using a 1% Ni cut-off, a minimum thickness of 2 metres, and a dry density of 1 g/cm 3 . Within the measured resources, the start-up pit, El Inicio, with more than 5M tonnes grading 2.1% Ni and 0.08% Co has been identified, with material from this pit being used to prove the metallurgical flowsheet. Essentially, there have been four processes used for the recovery of nickel and cobalt from laterite deposits. Two of these are pyrometallurgical processes (ferronickel production and matte smelting), and are not discussed any further in the context of this paper, except to note that these processes generally treat only the higher Ni, higher Mg-content saprolite horizons. One, the Caron Process, is a hybrid, being a reduction roast followed by ammonia leaching. The fourth is the only true hydrometallurgical process, pressure sulphuric acid leaching. The latter two processes focus mainly on the lower Ni, lower Mg-content limonite horizons. Over the past decade, nickel laterites have received a great deal of attention in terms of hydrometallurgical flowsheet development. All of the processes planned or so far commercialized have been based on a sulphuric acid leach at high pressure, the Pressure Acid Leach (PAL) or High Pressure Acid Leach (HPAL), and from published information, there appears to have been very little attention given to evaluating a chloride-based approach. Various reasons have been advanced for this, such as exotic materials of construction being needed, chloride is an aggressive lixiviant with a consequent high acid consumption and leaching of most metals in the ore, difficulties with controlling iron leaching, and how to handle magnesium leaching. All of these are valid concerns, but neither are they insurmountable problems. The first, and probably most successful, laterite leach plant is that at Moa Bay in Cuba, which originally (briefly) commenced operations in 1959 [2]. The process is based on a sulphuric acid pressure leach at around 240 o C in pachuca autoclaves, and subsequent precipitation of a mixed nickel/cobalt sulphide intermediate for further refining at the Corefco (formerly Sherritt) nickel- cobalt refinery at Fort Saskatchewan, Canada. Until relatively recently, this remained the only operating pressure acid leach process for nickel laterites. An alternative process, a modified version of that first described by Caron in 1950 [3,4] and known by his name, based on ammonia/ammonium carbonate leaching of reduction-roasted laterite, has seen some commercial success, notably by Níquel Tocantins in Brazil and Queensland Nickel (BHPBilliton) in Australia, although there have been other operations using this process. Its major disadvantage is that cobalt recovery is limited, often as low as 40%. The Sechol development in Guatemala is adjacent to the Exmibal property, owned by Inco, and operated as a nickel matte smelter until it shut down in 1980. These properties border Lake Izabal (Figure 2), which is increasingly becoming a resort spot, and therefore, it was considered undesirable to consider any kind of smelting operation in such a setting. Despite the relatively high MgO content of the ore, this not only eliminated options such as ferronickel or a continuation of matte smelting, but also the roasting step which is a pre-requisite for the Caron ammonia leach process. With this in mind, attention was then turned to investigating a hydrometallurgical flowsheet, with the original intention being to follow the well-developed sulphuric acid pressure leach (PAL, HPAL) processes in Western Australia, and which Inco has planned for the Goro Project in New Caledonia. Initial scoping testwork, carried out at different testing laboratories (and hence on slightly different materials), showed that both the saprolite and the limonite horizons of the Sechol orebody were amenable to leaching with either sulphuric or hydrochloric acid, as shown below in Table II. These tests were carried out in order to give pointers as to the most attractive route to follow, and the results can be summarized as follows: 3⁄4 The highest extractions were obtained with the pressure sulphuric acid leach system, although, as can be seen, the ...

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Citations

... Atmospheric leaching processes for nickel laterite ores have been studied extensively in the last two decades (McDonald and Whittington, 2008a, b;Stanković et al., 2020;Willis, 2012). The use of hydrochloric and nitric acid is considered to be more promising than sulphuric acid as they allow the acid to be regenerated and recycled and offer the potential to generate revenue in the form of high-grade magnesia through pyrohydrolisis (Brock and McCarthy, 2013;Harris and Magee, 2003;Harris and White, 2011). It follows that the largest operating cost component for nitrate and chloride processes is energy consumption. ...
Article
In this study, the potential of tailings generated from hydrometallurgical processing of nickel laterite ores as a source of scandium was investigated. The use of an atmospheric leaching process was proposed and five different lixiviants, namely sulphuric, phosphoric, oxalic, citric and ascorbic acids, were examined systematically to extract the scandium. Characterisation results showed that the nickel laterite residue sample contained about 148 ppm scandium and that the major crystalline phases of the sample were quartz, chromite, magnetite and akaganeite. Results of the leaching experiments suggested that most of the scandium was hosted within the refractory iron-bearing minerals, namely magnetite and chromite, based on the apparent correlation between the scandium dissolution and iron and chromium dissolutions and the composition of crystalline phases in the leached residues. Oxalic acid was found to be the most effective lixiviant to overcome the refractoriness of these minerals and render the scandium accessible for dissolution. To further improve the leaching performance with oxalic acid, the effects of acid concentration, stirring speed, pulp density, temperature and leaching duration on the leaching efficiency were studied. It was found that the scandium dissolution can reach up to 94% in 0.75 mol/L of the acid at a temperature of 95 °C, pulp density of 100 g/L, leaching time of 24 h and stirring speed of 600 rpm. These results demonstrated that the simple, atmospheric leaching process with an organic acid is feasible to extract scandium from nickel laterite residues.
... As such, HPAL is suitable only for treating limonite ores often leading to minimal utilisation of the saprolite component in the ore bodies. Given these problems, there is a growing interest in novel leaching techniques particularly those operating at atmospheric pressure conditions to make lateritic nickel ores more economically attractive [2][3][4][5][6][7][8][9][10][11][12]. ...
... It has been demonstrated that atmospheric pressure acid leaching using hydrochloric acid as lixiviant, such as the Neomet process, can produce nickel and cobalt recoveries comparable to HPAL [4]. One of the major drawbacks of the use of this acid is that it has poor selectivity against iron and therefore, dissolves essentially all iron in the ores along with nickel and cobalt resulting in high level of ferric chloride in the pregnant leach solution [9,14,15]. ...
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The effects of leaching parameters on the metal dissolutions from Caldag laterite ore using hydrochloric acid at atmospheric pressure were investigated. The following leaching parameters were examined to understand their effects on the dissolution of the metals: hydrochloric acid concentration, solid/liquid ratio, particle size, leaching temperature and time. Extractions of 95.8%Ni, 94.5%Co and 94.3%Mn into the leach solution were obtained along with a substantial amount of iron (81.5%) under the following conditions: 3.0 M HCl concentration, 90°C leaching temperature, 8 h leaching time, 1/5 solid/liquid ratio and −0.053 mm particle size. The hydrochloric acid consumption under these optimum conditions was found to be 543 kg t–1 ore. The results indicated that hydrochloric acid concentration and leaching temperature were the most important parameters affecting metal dissolutions. It was found that the dissolution of nickel did not exhibit a good linear correlation to that of manganese, which suggested that considerable amounts of nickel were not hosted in asbolane phase but also in other mineral phases such as goethite, haematite and clays. It was, however, found that most of the cobalt appeared to be hosted in asbolane. The semi-quantitative mineral analyses revealed that mineral dissolution order was as follows: calcite > goethite > haematite > lizardite ≥ chlorite-serpentine > asbolane > albite > kaolinite.
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The preparation of ferronickel alloy from the nickel laterite ore with low Co and high MgO contents was studied by using a pre-reduction–smelting method. The effects of reduction time, calcination temperature, quantity of reductant and calcium oxide (CaO), and pellet diameter on the reduction ratio of Fe and on the pellet strength were investigated. The results show that, for a roasting temperature >800 °C, a roasting time >30 min, 1.5wt% added anthracite coal, 5wt% added CaO, and a pellet size of ~10 mm, the reduction ratio of Fe exceeds 70% and the compressive strength of the pellets exceeds 10 kg per pellet. Reduction smelting experiments were performed by varying the smelting time, temperature, quantity of reductant and CaO, and reduction ratio of Fe in the pellets. Optimal conditions for the reduction smelting process are as follows: smelting time, 30–45 min; smelting temperature, 1550°C; quantity of reductant, 4wt%–5wt%; and quantity of CaO, 5wt%; leading to an Fe reduction ratio of 75% in the pellets. In addition, the mineral composition of the raw ore and that during the reduction process were investigated by process mineralogy.
... 2 This activity augmentation in concentrated chloride systems, first reported in Ref. 3, has repeatedly been referenced as a motivating factor behind chloride hydrometallurgy. 1,[3][4][5][6][7][8] This activity increase allows a similar amount of acid to achieve a lower pH in a concentrated solution than in a dilute solution, and therefore be more effective. Falconbridge's Matte Leach Process pioneered the use of chloride chemistry to recover Ni in the early 50s. ...
... Although leaching of lateritic saprolites in chloride media has been studied before, this has been done in more dilute brines, less than 300 g L 21 total chloride, which allows hydrolysis of the iron within the leaching step. 4,5 Recovery of HCl by precipitation of magnesium hydroxychlorides however requires concentrations of at least 300 g L 21 total chloride, and it was leaching in these solutions which was investigated here. ...
... All soluble metals except Mg displayed similar and high extractions in the aqueous HCl experiments, showing the ability of the MgCl 2 brine to suppress Mg dissolution from the ore while achieving greater than 95% extraction of Ni and Co. At this low concentration (or activity) of water, iron is not hydrolyzed to hematite, likely due to the large chloride concentration, greater than 325 g Cl 2 /L, and the subsequent formation of FeCl 4 2 complexes. 4,5,9 The kinetics of the leaching reaction were determined from liquid phase samples and a representative extraction curve is shown above in Fig. 3. Owing to the high levels of background Mg in the MgCl 2 brine it was not possible to determine the kinetics of Mg extraction. ...
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... Much previous work has been done on chloride leaching of saprolite ores. The experience of the Magnola process, with further development in the Jaguar Process along with work by such companies as Intec, indicates that silicate ore dissolves readily in a strong hydrochloric acid leach [1][2][3][4][5]. The leach brings almost all the metal ions into solution as chlorides while leaving behind the silica as a solid: ...
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HCl leaching using molten salt hydrates has the potential to improve the extraction of nickel from laterite ores. However, as in other HCl leaching applications, recovery of HCl is key to process economics. Spray pyrohydrolysis, which is used in current chloride-based flowsheets, is associated with a high energy cost. The authors have developed a proposed laterite leach circuit using an alternative HCl recovery route. The leach circuit envisions a leach by concentrated (33%) HCl in an MgCl 2 molten salt hydrate (MSH) or brine medium, followed by Ni/Co recovery and iron precipitation. Magnesium and chloride are precipitated from solution as magnesium hydroxychloride; this hydroxychloride is thermally decomposed to produce HCl gas. The proposed flowsheet employs a chloride leach circuit with simpler equipment and lower energy cost than in the conventional practice of pyrohydrolysis. Laboratory work investigated key aspects of the flowsheet, including precipitation of magnesium hydroxychlorides and their composition; magnesium hydroxychloride thermal decomposition; and iron control.
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... When first presented, it seemed that Jaguar Nickel's Atmospheric Chloride Leach Process (ACLP) might be able to overcome some of the problems inherent in the hydrometallurgical processing of nickel laterite ores. The publications from Jaguar Nickel [1,2,3,4] as well as the patent application [21] show that one of the two key original concepts of the high-concentration chloride laterite leaching circuit was the simultaneous (or, more correctly, sequential) leaching and precipitation of iron in the leach reactors, using the properties of the concentrated magnesium chloride brine matrix and the inherent alkalinity of, particularly, the saprolite fraction of the ore. This was intended to permit a very low addition rate of hydrochloric acid to be used at no higher than 150 kg/tonne dry laterite [4]. ...
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