The Distribution, Character, and Rhenium Content of Molybdenite in the Aitik Cu-Au-Ag-(Mo) Deposit and Its Southern Extension in the Northern Norrbotten Ore District, Northern Sweden

Molybdenite in the Aitik deposit and its southern extension was studied through mineralogical/chemical analysis and laboratory flotation tests. It is demonstrated that molybdenite varies considerably in grain size, ranging from coarse (>20 μm) to very fine (<2 μm) and occurs predominantly as single grains in the groundmass of the rocks, as grain aggregates, and intergrown with chalcopyrite and pyrite. The dominating molybdenite-bearing rocks are the mica schists, the quartz-monzodiorite, and the Salmijärvi biotite-amphibole gneiss, the latter containing mostly medium-coarsegrained OPEN ACCESS Minerals 2014, 4 789 molybdenite. Later geological features, such as garnet-magnetite-anhydrite-K feldspar alteration and pegmatite dikes appear to be responsible for a significant part of the distribution pattern of molybdenite. Molybdenite grains contain up to 1587 ppm Re, with an average of 211 ± 10 ppm in Aitik molybdenite and 452 ± 33 ppm in Salmijärvi molybdenite. The higher Re concentrations are found in molybdenite associated with sericiteand quartz-amphibole-magnetite altered rocks, whereas low Re values occur in rocks in which potassic alteration is prominent. Molybdenite recovery is influenced by the mineralogy of the host rock and the alteration grade; hence both of these factors will have an impact on potential recoveries. The recovery of molybdenite was lower from flotation feeds with significant amounts of Mg-bearing clay-micas.


Introduction
The Aitik porphyry Cu-Au-Ag-(Mo) deposit is located 60 km north of the Arctic Circle at latitude 67°04'N and longitude 20°57'E in the Gällivare area in northern Sweden ( Figure 1). The mineralization extends for ~5 km with a maximum width of 400 m, and is known to extend to a maximum depth of 800 m in the deepest investigated parts ( A major mine expansion program for Aitik has recently been finished to reach 36 Mt of annual ore production, and a decision to go for 45 Mt capacity was taken in early summer 2014. Future plans for the Aitik mine also include a study which will assess the possibility of commencing molybdenum extraction. To date, no studies have been performed on the occurrence of molybdenite within the ore body, a detailed characterization of this mineral is essential in order to maximize future recovery of molybdenum. With current metal prices it is important to characterize the ore body of its minor components and to map and characterize metallurgical parameters that could affect the ore value, regardless if the minor component constitutes a penalty metal or a bonus metal. Since rhenium occurs naturally in molybdenite [1], extraction of molybdenite through flotation would yield a rhenium-bearing molybdenite concentrate that has a potentially higher market value.  [2]). Inset shows the location of the Gällivare area (rectangle) and the Aitik deposit (star) within the Fennoscandian Shield.
The Aitik and Salmijärvi ore bodies that are presented by this study are Palaeoproterozoic deposits which have been modified by multistage metamorphic-tectonic and magmatic-hydrothermal events. Redistribution of metals and possible addition of ore minerals from a later mineralizing event has led to a wide variety of mineralization styles and a complex mineralization pattern [3]. This pattern has been studied in detail regarding copper, and to some extent gold [4,5].
In this paper, we describe the character of molybdenite in the Aitik deposit, and demonstrate the application of qualitative and quantitative mineralogical data derived from optical microscope, QEMSCAN (Quantitative evaluation of minerals by scanning electron microscopy) and ICP-MS (Inductively coupled plasma mass spectrometry) to genetic and mineral processing issues. The results will form an integral part of the input required for a future blockmodel where the geological, mineralogical and metallurgical character of the ore is combined, and the true value of this deposit assessed accurately.

Geology
The Aitik porphyry Cu-Au-Ag-(Mo) deposit and its host rocks, situated ~200 km north of the Archaean-Proterozoic palaeoboundary in the Fennoscandian shield, are understood to have formed in a volcanic arc environment related to subduction of oceanic crust beneath the Archaean craton at ca. 1.9 Ga [7]. A quartz monzodioritic intrusion related to the formation of porphyry copper mineralization is situated in the footwall of the deposit (Figure 2). This source intrusion and related volcaniclastic rocks are mafic-intermediate in composition and belong to the regionally widespread Haparanda suite of intrusions and the Porphyrite group of volcanic rocks, respectively [8]. The deposit is overprinted by a hydrothermal event of Iron Oxide Cu-Au (IOCG) type at ca. 1.8 Ga [3] and strongly deformed and metamorphosed at amphibolite facies, resulting in at least 160 Ma of post-ore modification [9].

Deposit Geology
The Aitik quartz monzodiorite intrusion is comprised of younger, comagmatic, intrusions of micro-quartz monzodiorite and diorite, and is suggested to represent a cupola protruding from a pluton at depth [7]. It is typically grey and plagioclase-porphyritic with a medium grained groundmass of plagioclase, biotite, K-feldspar and quartz, and trace amounts of titanite, apatite and zircon [7]. It should be noted that the quartz monzodiorite intrusion is metamorphosed, and should accordingly be called gneiss. However, in order to stress the intrusion-related origin of the deposit this has not been applied below.
The surrounding volcaniclastic rocks constitute feldspar-biotite-amphibole gneisses in the footwall and hanging wall, and quartz-muscovite schist and biotite schist/gneiss in the ore zone ( Figure 2). The feldspar-biotite-amphibole gneiss in the footwall to the ore is composed of large (6000 to 20,000 μm) amphibole phenocrysts in a groundmass of feldspar, biotite and amphibole, with accessory apatite, titanite, zircon and opaque phases. The hangingwall feldspar-biotite-amphibole gneiss is grey-greenish to grey-brownish in color and fine-grained (~200 μm). Abundant accessory magnetite and titanite occur in a groundmass of plagioclase, biotite, amphibole and quartz. The hangingwall gneiss is separated from the ore zone by a thrust (Figure 2).
The dominant rock type in the ore zone is the light grey, garnet-bearing biotite gneiss with approximately 1% to 2% garnet porphyroblasts. The microcrystalline groundmass contains K-feldspar, plagioclase, biotite, amphibole, quartz, and opaque minerals, and accessory minerals that include tourmaline, apatite, fluorite and titanite. The quartz-muscovite schist is commonly sericite-altered and mainly comprises muscovite, K-feldspar, quartz, sericite and tourmaline, with accessory apatite and opaque phases. Pyrite is common. Lenses of micro-quartz monzodiorite can be distinguished within less foliated sections of the ore zone schist and gneiss.
Several generations of pegmatitic dykes, barite veins, and quartz-sulfide veins occur in the Aitik mining area. The pegmatites strike either north-south or east-west and range in thickness from 0.5 to 20 m. Pegmatites within the ore zone and footwall frequently contain pyrite and chalcopyrite, and occasionally molybdenite, in addition to plagioclase, quartz, microcline, muscovite, biotite and tourmaline. Pegmatite dykes in the hangingwall are predominantly barren. Pegmatites striking north-south, i.e., along the main foliation, in places display deformation features such as folding, while those crosscutting the foliation in an east-west direction, are always underformed. Ages of pegmatite dykes range between 1850 to 1730 Ma [9].
The main copper-bearing mineral at Aitik is chalcopyrite, which is often disseminated. Bornite and chalcocite are present in trace amounts. Other ore minerals include pyrite, magnetite, pyrrhotite, ilmenite, molybdenite, gold, and silver. Molybdenite is sporadically observed in the ore zone and footwall of the deposit, usually in association with chalcopyrite and/or pyrite, in quartz veins of varying composition, and as coarse aggregates within pegmatite dykes. Gold occurs as native metal in amalgam and in electrum [5], in close association with groundmass minerals such as K feldspar, biotite, plagioclase and quartz, but also with chalcopyrite and pyrite [10]. To date, the distribution of silver and its mode of occurrence has not been studied in detail, but the majority of the silver is likely to be hosted within the chalcopyrite [11].
Salmijärvi constitutes the southern extension of the Aitik ore body and comprises of strongly altered and metamorphosed biotite gneiss, amphibole-biotite gneiss and amphibole gneiss within the ore zone ( Figure 2). These gneisses seem to be of slightly higher metamorphic grade and/or more strongly hydrothermally altered than the rocks in the Aitik main ore zone, although show similar folding styles and well developed foliations. As with the Aitik ore body, the Salmijärvi ore is crosscut by weakly mineralized pegmatite dykes and occasional quartz dykes. Quartz monzodioritic bodies occur on the footwall side of the ore (Figure 2). The hanging wall rocks consist of the same hornblende-banded garnet-porphyroblastic amphibole gneiss. In the ore zone, westward, the biotite gneiss becomes more schistose [12]. Commonly there are mm-to cm-sized green hornblende veinlets, surrounded by albite haloes within the Salmijärvi area. These veins often have a central line of chalcopyrite and are rimmed by quartz and feldspar, i.e., very similar to the footwall mineralization in the Aitik main pit. The hornblende veins are often short (dm-size), sometimes with a vuggy appearance [13]. The contact between the ore zone and the hanging wall rocks is sharp and dipping 60° to the west, whereas the western ore body contact is grade controlled and thus gradational. The hanging wall contact is curved and the ore body pinches out towards the south. The contact can be seen cut by thin pegmatite dykes. The muscovite schist with common pyrite in Aitik is absent in Salmijärvi. The majority of the molybdenite is associated with quartz veins/blebs of slightly varying composition. Molybdenite occurs as small grains and clusters within mm to cm sized quartz veinlets, within mm to cm away from the quartz veins, and within dm sized quartz blebs. The quartz veins form a weak stockwork which often contains pyrite and chalcopyrite as well. The quartz stockwork forms 1%-5% of the host rock. Molybdenite also occurs as trace dissemination in the host rock.

Sampling and Methods
Sixty-four samples were taken from 33 drill cores from the Salmijärvi and Aitik deposits, and from the Aitik open pit. Samples were taken from different lithologies and alteration-and mineralization assemblages. Samples contained molybdenite that was both visible and not visible by the naked eye. Polished thin sections were prepared by Vancouver Petrographics Ltd, Langley, Canada, and were examined in detail to document wall rock, alteration-and mineralization phases. In order to document and characterize the different molybdenite mineralization phases, a detailed optical examination of polished thin sections in reflected and transmitted light using a standard petrographic microscope (Nikon ECLIPSE E600 POL, Nikon Instruments, Amsterdam, The Netherlands) was conducted before and after QEMSCAN, ICP-MS, and flotation analyses.

QEMSCAN Analysis
In order to assess all size fractions, and thereby obtain a reliable compilation of the overall molybdenite content at Aitik and Salmijärvi, and to be able to search a large number of samples, QEMSCAN analyses were performed. Identification of molybdenite in 30 polished thin sections by X-ray and image analysis was performed at the QEMSCAN laboratory of Intellection UK in North Wales. Polished thin sections were measured using a fieldscan operating mode with a beam-stepping interval of 25 μm. Fieldscan analyses are based on between 578,797 and 767,112 individual EDS (Energy-dispersive X-ray spectroscopy) analyses per thin section. Samples were then analyzed using the trace mineral search (TMS) mode. The backscatter electron threshold was set at 115 so that any grains "brighter" than chalcopyrite (e.g., molybdenite) were identified, and the selected grains and surrounding area were mapped using a beam-stepping interval of 1 μm. Thirteen complementary samples were analyzed at the QEMSCAN laboratory of LKAB MetLab in Luleå, Sweden. Polished thin sections were measured using the trace mineral search (TMS) mode with a beam-stepping interval of 5 μm. The backscatter electron threshold was set at 121. Fieldscan analyses were performed on specific areas that were re-mapped using a beam stepping interval of 1 μm. Some of the molybdenite grains (ca. 100-150) detected by QEMSCAN were re-located in the optical microscope in order to study mineral associations and related textures in more detail.

Molybdenite Re Abundance Determination
Seventeen drill core samples with visible molybdenite were selected for dilution ICP-MS analysis in order to determine the rhenium content of individual molybdenite grains (Table 1). Localized variation in Re abundance in the molybdenite grain [14][15][16] was avoided by isolating the entire area of molybdenite. Selection of molybdenite grains was done in polished thin sections together with their copy of rock chips using a high magnification Nikon Microscope at the Division of Geosciences at Luleå University of Technology, Sweden. Grains were chosen so that a variety of sizes, mineral associations and host rocks would be represented. Sampled molybdenite were extracted from the rock chips using a New Wave™ (Fremont, CA, USA) micro drill at Arthur Holmes Isotope Geology Laboratory (AHIGL) which is part of the Durham Geochemistry Centre at Durham University, UK.
The Micro drill instrument contains three basic parts; a Binocular Microscope, a high speed drill with adjustable tungsten carbide and an XYZ stage. All the components are integrated with a workstation allowing for high precision (±1 μm) movement of the drill. See [17] for further details of the microdrill setup.
Rock chips containing grains of molybdenite were first attached and mounted with double sided tape on the sample plate stage. Molybdenite was sampled using ca. 30 μm diameter drill bit and a 40 μm drill depth. Depending on grain size, several samples were taken from each grain in order to maximize the recovery of molybdenite. After each grain was sampled, the rock chip was cleaned in an ultrasonic bath in ethanol [17] and the drill bit replaced in order to avoid contamination.
Recovery of the molybdenite separate was achieved using a flotation technique with high purity water (MilliQ, Darmstadt, Germany) by a 0.5-10 μL micropipette which sucked up the floated molybdenite grains or dry separation technique (to minimize impurities such as quartz, biotite, amphibole, chalcopyrite, pyrite and magnetite) using a high magnification microscope. A total of 27 molybdenite grains were individually weighed on a gold boat using a Mettler Todeo UMT2 balance (Mettler-Toledo Ltd., Leicester, UK). The weight of the samples extracted for analysis ranged from 0.001 to 0.088 mg ( Table 1). The molybdenite was washed from the gold boat in a 3.5 mL savillex vial with 0.25 mL of concentrated HCl at 80 °C overnight (>12 h). Following this stage the gold boat was removed from the vial. The molybdenite in 0.25 mL of concentrated HCl was then digested in a known amount of 185Re tracer solution together with 0.5 mL concentrated HNO3 at 130 °C for ~24 h. Following digestion the sample was evaporated to dryness at 80 °C and then prepared for ICP-MS analysis by the addition of 1 mL 0.8 N HNO3.

Laboratory Flotation Tests
To investigate the flotation response of different ore types (with variable molybdenum content) in the Aitik deposit, laboratory flotation tests were performed on 14 drill core samples after 7 and 11 min of grinding. Samples consist of approximately 10-15 kg of drill core each. Metallurgical testing was performed at the mineral laboratory of the Processing department (TMP) at Boliden Mineral.
Samples were obtained from representative, homogenous sections in drill cores. Drill cores were chosen so that sampling would cover the major lithologies and alteration-and mineralization types present in Aitik (except pegmatite dykes), and all samples were studied and documented in detail in hand specimen and polished thin sections before grinding. Molybdenite was not visible by the naked eye in any of the samples. Each sample was passed through a 3 mm screen and the oversize was crushed to below 3 mm. The sample was then split into 1 kg posts and stored for further treatment.
At each test, 1 kg of material was placed in a laboratory rod mill with an 8.0 kg rod charge and 550 mL of water. A Φ 195 mm × 245 mm stainless steel mill was used, rotating with 48 rpm. The diameters of the stainless rods are varying continuously from a maximum of 25 mm, down to about 5 mm. 7 and 11 min grinding time were chosen, generating particle size distributions (PSD: s) similar to a distribution from the Aitik plant. The laboratory rod mill produces less coarse particles than the autogenous grinding circuits in the plant but this does not normally affect the results.
After grinding, the pulp was transferred to a 2.5 L flotation cell. Flotation trials were conducted in a Wemco laboratory flotation unit, with a mixing speed of 1200 rpm. Tap water was added and the pH noted varied between 8.0 and 8.7 in the different tests. After conditioning for 5 min at pH 10.5 with slaked lime, Cu rougher flotation tests were run in 4 sequential steps with 1, 2, 3, and 3 min flotation times. Before each flotation step, a 1-min conditioning time was allowed for adding 5 g/tonnes of collector, frother was added if needed. Potassium xanthate (KAX) is used as collector in Aitik. The frother is a glycol, ether/glycol mixture (Nasfroth 350). All flotation products were filtered and dried and the dry weight was noted.
Each test consisted of three parallel flotation tests for which a total of 3 kg material was needed. Through this methodology enough amounts of products were produced for the assaying. Flotation products were analyzed with X-ray for a multitude of elements including Cu, Mo and S. This work was done at the Aitik process laboratory and required 12 g of each product.

Results
By performing petrographic, QEMSCAN, ICP-MS, and flotation laboratory test studies on molybdenite, the diversity of its character, occurrence, and rhenium content, and its response to the standard copper flotation procedure used for the Aitik ore has been thoroughly characterized. In the studied area, molybdenite grain size varies from coarse (>20 μm) to very fine (<2 μm) and occurs mainly as single grains in the groundmass of the rocks, as grain aggregates, and as intergrowths with chalcopyrite and pyrite. The molybdenite-bearing rocks are the biotite-and muscovite schists in the Aitik ore zone, the quartz monzodiorite in the Aitik footwall, and the Salmijärvi biotite-amphibole gneiss, the latter containing mostly medium-coarse grained molybdenite. In summary the rhenium abundance of molybdenite varies between 20-1587 ppm, with the higher contents obtained from Salmijärvi molybdenite samples.

QEMSCAN Analysis of the Distribution and Character of Molybdenite
Of the 36 samples from Aitik analyzed by QEMSCAN, 26 contain molybdenite and a total of 8336 molybdenite grains were found. The majority of molybdenite grains occur as 10-100 μm rectangular or subrectangular flakes lying individually or intergrown with each other (Figure 3a). Molybdenite grains in Aitik are dominantly associated with anhydrite, chalcopyrite, pyrite, biotite and K feldspar in mica schists and in quartz monzodiorite (Figures 3a-c and 4), and occasionally in pegmatite. The richest sample, containing 3047 molybdenite grains, is garnet-magnetite-quartz-anhydrite-altered biotite schist dominated by biotite, anhydrite, tourmaline and feldspar with minor sulfides. A similar sample, containing 2311 molybdenite grains, is an amphibole-quartz-sulfide-altered quartz monzodiorite, with amphibole, zeolite, quartz and anhydrite. The overall grain size distribution of molybdenite grains in Aitik is shown in Figure 5.  Of the seven samples from Salmijärvi analyzed by QEMSCAN, five contain molybdenite and a total of 549 molybdenite grains were found. Molybdenite grains occur mainly as 7-185 μm rectangular and rounded flakes dominantly associated with K feldspar, quartz, plagioclase, and sulfides in biotite gneiss and bioite-amphibole gneiss, and occasionally in pegmatite. The richest sample, containing 538 molybdenite grains, is a K feldspar-altered biotite gneiss with sporadic sulfide-magnetite-apatite-alteration patches. A grain size distribution built upon the type of alteration present is clearly outlined in this sample, with grains ≤10 μm mainly associated with K feldspar, quartz, and biotite, and grains 10-185 μm associated with chalcopyrite, pyrite, magnetite, K feldspar, quartz, biotite, and apatite ( Figure 3d). The overall grain size distribution of molybdenite grains in Salmijärvi is shown in Figure 5.

Rhenium Abundance of Molybdenite
The rhenium content of molybdenite grains from the two studied deposits show significant variation (20 to 1587 ppm) as summarized in Table 1. In Figure 6, the concentration of rhenium measured in each grain is presented in relationship to the setting of the grain (associated host rock, and alterationand mineralization type).
In Aitik, an average Re content of 211 ± 10 ppm (4.7% 1σ, n = 15) is obtained. Samples of garnet-bearing biotite gneiss and pegmatite generally contain molybdenite with low concentrations of Re (on average 116 and 117 ppm, respectively) while samples of quartz monzodiorite and quartz-muscovite-(sericite) schist generally contain higher concentrations of Re in molybdenite (on average 334 and 310 ppm, respectively, Figure 6a). Molybdenite from two generations of pegmatite dykes were analyzed and revealed a low-Re concentration for molybdenite within the old (ca. 1.85 Ga) and deformed pegmatite dyke, and a medium-Re concentration for molybdenite within the young (ca. 1.73 Ga) and cross-cutting pegmatite dyke (Table 1). In Salmijärvi, an average Re content of 452 ± 33 ppm (7.3% 1σ, n = 10) is obtained. Samples of amphibole-(biotite) gneiss generally contain low-Re molybdenite (on average 155 ppm) while samples of biotite-(amphibole) gneiss contain high-Re molybdenite (on average 650 ppm) (Figure 6a).  In Aitik, the Re content of all molybdenite grains associated with sericite (either sericite replacing plagioclase in the quartz monzodiorite or sericite replacing muscovite in the quartz-muscovite schist) are high (commonly above average) and ranges from 191 to 784 ppm (alteration assemblage groups a and d in Figure 6b), whereas the rhenium content of molybdenite grains associated with quartz-(kf-am) ranges from 20 to 289 ppm (alteration assemblage groups a-c, e and f in Figure 6b). In Salmijärvi, the rhenium content of all molybdenite grains associated with a quartz-amphibole-magnetite alteration assemblage, with or without other minerals such as feldspar, chlorite, calcite, epidote, and zeolite, are high (commonly above average) and ranges from 367 to 1587 ppm (alteration assemblage groups b and c in Figure 6b), whereas the rhenium content of molybdenite grains associated with K feldspar, biotite, and amphibole ranges from 46 to 223 ppm (alteration assemblage groups a-c in Figure 6b).

Molybdenum Flotation
The Mo recovery after 11 min grinding time did not substantially differ from that achieved after 7 min grinding time. The laboratory test Mo total recoveries resemble the plant recoveries to the Cu concentrate. The laboratory total recoveries are presented in Figure 7. Production results representing daily Mo recovery to Cu concentrate from nearly 2.5 years of production is presented in the same figure as limitation curves for high and low results. The expected Mo recovery is shown also. Three drill core samples with low Mo recoveries are marked out in the figure with the two last digits in the TMP sample number. These are nos. S-6792, S-6783 and S-6786. Three drill core samples with high Mo recoveries are also marked out (sample nos. S-6780, S-6785 and S-6789). The flotation recoveries together with a geological description of each test sample are presented in Table 2.  Table 2 below.

Discussion
Porphyry systems are the most important source for molybdenum and rhenium in the world. These deposits alone account for more than 95% of molybdenum production [19]. Based on the relative content of copper and molybdenum, the porphyry deposits are divided into two categories: Cu ± Mo deposits and Mo ± Cu deposits [20]. In the copper dominant systems the molybdenum grade generally ranges from 0.005%-0.03%, while in the molybdenum dominant it ranges from 0.07%-0.3% [19,21].
The rhenium concentration in molybdenite in porphyry systems varies from the ppb level to thousands of ppm [22,23]. In Figure 8, the average rhenium content in the Aitik and Salmijärvi ore bodies are compared with those reported from other porphyry Cu and Cu-Mo deposits in the world. These deposits exhibit a relatively low quantity of molybdenite, and generally contain higher concentrations of rhenium than porphyry Mo-Cu deposits with abundant molybdenite. This may relate to the fact that small amounts of molybdenite will consume the limited rhenium budget from the ore-forming fluids whereas rhenium within large volumes of molybdenite-rich magma will be relatively diluted [14,24,25]. The Aitik and Salmijärvi deposits show similar trends in Re grades as Cu-Mo deposits in general (Figure 8).  [22].
In Aitik, with its complex multi-magmatic/hydrothermal history [3], molybdenum has probably been introduced by several generations of magma, as indicated by Re-Os ages of 1.87, 1.85, and 1.73 Ga obtained for molybdenite in barite and pegmatite dykes in the Aitik ore zone [9]. These ages correspond to the Haparanda, Jyryjoki, and TIB2 magmatism, respectively, which are well-constrained magmatic events in northern Fennoscandia [26]. However, some molybdenite formation might also be the result of late hydrothermal activity and metamorphism. The authors of [27] describe a metamorphic dehydration process active in northern Sweden during the Svecofennian orogeny which produced small Mo-(W) occurrences with characteristic low-Re molybdenite formation. The Liikavaara Cu-Au occurrence, situated only 4 km east of Aitik, contains molybdenite-and scheelite-bearing quartz-and aplitic veins [28]. Its close spatial relationship to Aitik implies that fluids responsible for the Liikavaara Mo-W mineralization might also have affected the Aitik deposit and its southern extension, with possible addition of (low-Re) molybdenite as a result.
Regarding the distribution of molybdenite within the Aitik ore body, molybdenum grades are higher in the northern part of the ore body than in the southern part ( Figure 9). One explanation to this pattern may be the distribution of variably altered host rocks, since certain alteration types and associated veining, rather than a specific rock type, seems to be an important factor controlling the distribution of molybdenite in Aitik.
The majority of studied molybdenite grains are found within mica schists and quartz monzodiorite, and coarser molybdenite grains (>50 μm) are exclusively found in samples of these rock types (Figure 4). The mica schists, and especially the quartz-muscovite-(sericite) schist, are nearly absent towards the south and towards depth (Figure 2), thus partly explaining the large-scale distribution pattern (Figure 9). The quartz monzodiorite is the source intrusion to the Aitik mineralization [7] and the mica schists and gneiss are co-magmatic volcanosedimentary rocks that have been strongly altered and deformed [8]. Molybdenite mineralization in porphyry ore systems often occurs after the main Cu-Au mineralizing event [29]. In a recent study of the Bingham porphyry deposit, [30] describes a process of selective metal deposition from a magmatic fluid due to changes of redox and pH conditions associated with a more reducing environment in the fluid source. The molybdenite mineral associations revealed in this study however indicate opposite conditions (e.g., anhydrite, magnetite, see discussion below). Contrary to the more common Phanerozoic porphyry systems the Aitik and Salmijärvi ore bodies have been subjected to at least two metamorphic events, varying degrees of multiple deformation, and an overprinting hydrothermal event of IOCG-type [3], and the distribution and character of ore minerals as seen today is probably more the result of a combination of post-ore processes including recrystallization, remobilization, and mineral/element differentiation, rather than primary features. These processes are known to lead to both concentration and dispersion of valuable minerals and also to considerable variations in ore grade within a single deposit [31].
As mentioned above, molybdenite in Aitik is found in a wide variety of mineralogical associations, although an association with anhydrite dominates together with chalcopyrite, pyrite, biotite, K feldspar, pegmatite dykes, and barite-and quartz veins. The surprisingly strong association with anhydrite instead of expected quartz indicates that there might be more anhydrite in the deposit than previously thought, i.e., that anhydrite is mistaken for quartz/feldspar-alteration and veining when drill cores are being logged.
Molybdenite in Salmijärvi is dominantly associated with pegmatite dykes and late K feldsparepidote-quartz ± magnetite-alteration of the gneisses. The richest sample, containing 538 molybdenite grains, is a K feldspar-altered biotite gneiss with sporadic sulfide-magnetite-apatite-alteration patches of typical IOCG-character (iron-oxide copper gold). The size of molybdenite grains in Salmijärvi is significantly larger than those found in Aitik ( Figure 5), a feature that might be caused by the slightly higher grade of metamorphism implied for the Salmijärvi area [13]. In Salmijärvi, a coarsening of the molybdenite grain size seems to follow the degree of alteration, with the overprinting sulfide-magnetite-apatite-alteration containing most of the coarser grains. The relationship between grain size and alteration type, with grains ≤10 μm mainly associated with K feldspar, quartz, and biotite, and grains 10-185 μm associated with chalcopyrite, pyrite, magnetite, K feldspar, quartz, biotite, and apatite, indicates that even if the latter mineral association is not the most common one, it probably constitutes the largest mass of molybdenite due to the larger grain size, an observation with relevance for future processing of the ore. The strong alteration is of oxidized character, occasionally rich in goethite and magnetite, which gives the rock an easily recognized rusty red color. This alteration type has not been observed in the Aitik ore body.
It is clear that strong alteration and post-ore veins of variable composition, often in combination with patches and clots of remobilized Cu-Fe sulfides appear to favor the occurrence of molybdenite in Aitik and Salmijärvi. This is probably related to the hydrothermal fluid that causes the alteration, in combination with deformation, both of which would allow molybdenum to migrate [32]. Thus, less molybdenite is found in the biotite gneiss, which is less altered and less tectonically affected than the mica schists, an observation also made in the Archaean Cu-Au-Mo occurrences of the Chibougamau district, Québec [33].
In Aitik molybdenite, with an average rhenium concentration of 211 ppm, molybdenite hosted by quartz monzodiorite and quartz-muscovite-sericite schist generally contain higher concentrations of rhenium (on average 244 and 310 ppm, respectively) than those hosted by pegmatites and gneisses (on average 116 and 157 ppm, respectively). In fact, the rhenium content of all studied molybdenite grains associated with sericite, either sericite replacing plagioclase in the quartz monzodiorite or sericite replacing muscovite in the quartz-muscovite schist, are high (commonly above average) and ranges from 191 to 784 ppm, whereas the rhenium content of molybdenite grains associated with quartz-(K feldspar-amphibole) ranges from 20 to 289 ppm. The variation of rhenium in molybdenite from the Sar Cheshmeh porphyry Cu-Mo deposit, Iran, shows an increased rhenium concentration in molybdenite that is intimately associated with sericitic altered veins of low quartz content, whereas a low rhenium concentration is obtained for molybdenite in quartz veinlets showing strong silicification [34]. Other observations note high-rhenium in quartz-sericite-altered (phyllic) rocks and low-rhenium in K-feldspar/biotite-altered (potassic) rocks, and suggest an inverse relationship between the temperature of formation and the Re content of molybdenite [22]. Similar observations were made of molybdenite from the Bingham deposit [24]. As such, high-temperature, magmatic fluid may form low-rhenium molybdenite, similar to those grains analyzed from Aitik pegmatites and quartz-(-feldspar-amphibole)-clots, and a low-temperature, hydrothermal/metamorphic fluid could generate high-rhenium molybdenite such as the grains analyzed from Aitik muscovite-sericite schist and strongly sericite-altered quartz monzodiorite.
A similar pattern, although with molybdenite associated with a different mineral assemblage, is found in Salmijärvi where the rhenium content of all molybdenite grains associated with quartz-amphibole-magnetite alteration, with or without other minerals such as feldspar, chlorite, calcite, epidote, and zeolites, is high (commonly above the average 452 ppm) and ranges from 367 to 1587 ppm, whereas the rhenium content of molybdenite grains associated with K feldspar, biotite, and amphibole ranges from 46 to 223 ppm. This magnetite-rich alteration is common in Salmijärvi and Aitik and in many other metal-rich occurrences in the northern Norrbotten ore district (e.g., Nautanen and Tjårrojåkka) and is linked to the overprinting hydrothermal event of IOCG-type observed in the region [3]. Oxidizing fluids, which are favorable for transport of rhenium [35], might thus be partly responsible for deposition of high-rhenium molybdenite in Salmijärvi and Aitik, and just as with the distribution of molybdenite, certain alteration types rather than specific rock types can be of guidance when documenting the overall rhenium abundance in molybdenite-bearing deposits.
Molybdenite from two generations of pegmatite dykes analyzed in this study revealed a much lower rhenium concentration for molybdenite within the old (ca. 1.85 Ga) and deformed pegmatite dyke, than for molybdenite within the young (ca. 1.73 Ga) and cross-cutting pegmatite dyke (Table 1, Figure 6). The concentrations obtained (61 and 172 ppm, respectively) are in reasonable agreement with rhenium concentrations measured for Re-Os geochronological studies of the same pegmatite dykes by [9] giving values of 54 and 215 ppm, respectively. The concentration of rhenium in molybdenite is known to be a combination of several interplaying factors, e.g., composition of parent magmas and host rocks [14,22,36], degree of oxygen and chloride fugacity of the ore fluid [37], and changes in chemical and physical conditions during crystallization [22]. Reference [38] in their study of molybdenite in the Archaean Boddington Cu-Au deposit, Western Australia, also suggest that even though rhenium can remain locked in molybdenite under deformation, dissolution and reprecipitation may occur giving molybdenite a different rhenium concentration and grain size.

Processing Implications
Molybdenum is commonly recovered from copper concentrates in a process that starts with dewatering prior to the molybdenum circuit to get rid of excess reagents, followed by conditioning with a depressor for copper. The most common depressor is NaHS, sometimes in combination with cyanide. Finely ground activated carbon can be used to further remove excess of reagents and higher temperatures are sometimes used to promote the removal of collectors. Oxygen destroys the depressor to some extent and is avoided by using, e.g., nitrogen as the flotation gas. Regrinding of intermediate concentrates is normal to get better liberation and to make the froth easier to pump. Conventional flotation cells are used for rougher and scavenger flotation and quite often also for the first cleaners. Since the introduction of columns in the early 80's, more or less every molybdenum circuit has columns for the last cleaning steps. Due to the flaky character of molybdenite grains, with strong hydrophobic and inert faces and hydrophilic and reactive edges, additions of fuel oils to enhance the flotation is common practice. Molybdenum extraction from the molybdenite concentrate is performed by roasting of molybdenite at a temperature of 500-700 °C. During this process the molybdenum transforms to molybdenum trioxide and the rhenium stored within molybdenite transforms to rhenium heptoxide gas (Re2O7) [39]. The molybdenum recovery obtained by this process is less than 93%, generally ranging between 25%-85% [40].
The volatilized rhenium can be caught using a wet electrostatic system combined with dry apparatus, and transferred to a solution containing sulfuric acid, which leaches the rhenium from the enriched flue dust [39]. The separation of rhenium from this solution is achieved by sorption using ion-exchanges resins and/or liquid extraction [39,41] followed by addition of potassium chloride and ammonium chloride in order to precipitate or isolate rhenium elution in the form of perrhenate salts. The non-hazardous and stable ammonium perrhenate (NH4ReO4) is the common market product of rhenium. The rhenium recovery obtained by this process is generally less than 60% [40].

Mo Extraction
The possibility to recover molybdenum from the copper concentrate at Aitik has been investigated several times during the lifetime of the mine. The normal procedure with depression of chalcopyrite and other sulfides with NaHS as described in the previous section, has been proven to work for the Aitik concentrate [42].
However, even if Mo assays are obtained fast enough to be of guidance in process regulations (which is often not the case) they might not provide an accurate indication of recoverable molybdenum as long as factors influencing the extraction process are not defined and taken into account. In the current study, where one focus has been to identify lithological and mineralogical factors in the incoming ore which might affect molybdenum recovery, flotation laboratory tests reveal that three drill core samples resulting in Mo-recoveries lower than expected (−4% to −11%) considering the drill core Mo grades are from two different rock types ( Table 2): feldspar-biotite gneiss and biotie gneiss. These samples have three characteristics in common (1) they contain 30%-50% Fe-Mg micas (2) they contain rare quartz veinlets, and (3) they contain molybdenite grains of dominantly less than 10 μm size. QEMSCAN data of sample Aan1186-2B reveal that most mica is phlogopite, the Mg-rich end member of the biotite group. Chlorite in the same sample is of chamosite-composition (a Mg-Fe-rich member of the chlorite group), and a significant part of the minerals end up as unidentified Mg-minerals ( Figure 10). Furthermore, 63% of detected molybdenite grains are less than 10 μm. QEMSCAN data from four samples taken only 16-17 m downhole from Aan732-3A contain 445 molybdenite grains where 93%-100% are less than 10 μm.
In sample Aan1064-2A, giving a Mo-recovery almost as expected (+2%), approximately the same amount of mica is present (45%), although in the form of annite (Fe-biotite) and muscovite ( Figure 10). It is known that fine-grained mica minerals can disturb the flotation process by interfering in the separation of chalcopyrite and molybdenite [43]. Results from this study indicate that the mica composition may also be of significance. According to [44], there are four non-sulfide minerals in the Bingham Mine, Utah, that are negatively correlated with molybdenum recovery: talc, andradite, calcite and amphibole. These minerals contain Ca 2+ or Mg 2+ or both. Zanin et al. (2009) studied the effect of Ca 2+ and Mg 2+ in solution and gangue minerals on the recovery of molybdenite by performing laboratory flotation tests on coarse molybdenite particles from two different host rocks. They came to the conclusion that the adsorption of Ca 2+ and Mg 2+ to the edges of molybdenite particles may have the combined effect of reducing the hydrophobicity of molybdenite grains, and bridging to specific, negatively charged, gangue minerals in the slurry, possibly leading to the formation of slime coatings. The bridging effect was also shown to be dependent on the type of host rock [45].
Reference [44] furthermore identifies biotite/phlogopite as being positively correlated with molybdenum recovery, a finding that are not discussed further by [44], and that is in contrast to results presented in this paper and to the work by [43] where a number of clay-micas (e.g., chamosite) are identified as causing poor molybdenum recovery. Some drill core samples produced higher Mo-recoveries than expected. Looking at the three top samples (+8% to +13%), these also represent different rock types: quartz monzodiorite, biotite gneiss, and amphibole-feldspar-biotite gneiss, but they are all characterized by common quartz veins and quartz clots containing chalcopyrite and pyrite, a feature that is missing in the samples discussed above. The amount of mica minerals is limited in these samples ( Figure 10). Furthermore, no molybdenite was found when analyzing thin sections from two of these flotation samples by QEMSCAN. Since molybdenum grades are normal to high (26-111 ppm) in these samples, this probably indicates that the molybdenite is coarse grained and therefore difficult to trap in a thin section. One reason for the obtained results thus seems to be found in the geological and mineralogical character of the rock, i.e., the host rock lithology, the vein-and alteration types present, and the size of molybdenite grains, thus emphasizing the importance of careful characterization of ores, including the distribution and texture of both ore and gangue minerals, in order to develop optimized treatment processes.

Re Extraction
The possibility to recover rhenium from the molybdenite concentrate at Aitik has never been tested or investigated. As can be seen from the result of this work, the Aitik molybdenite contains on average 213 ppm Re, but this varies considerably between different particles (20-1587 ppm). High-Re molybdenite is mainly found in quartz monzodiorite and quartz-muscovite-sericite schist. The majority of molybdenite grains in Aitik are less than 10 microns though, and the quartz-muscovite-sericite schist disappears towards depth and towards south. Regarding the pegmatite dykes, these are due to their hardness occasionally separated from the ore to avoid low throughput. Their molybdenite and rhenium contents, although limited, could form an added value and thus motivate more of such handling, and perhaps change the mine cut-off grade. In Salmijärvi, however, the average Re content is higher (452 ppm), the size of molybdenite grains is larger, and the high-Re molybdenite is found within the common biotite-(amphibole) gneiss.
A mass balance prognosis for molybdenum concentrate production at Aitik is presented in Table 3. A Mo content of 0.0025% in the Aitik ore, and a recovery of ca. 85% to the copper concentrate can be assumed. Furthermore, a 60% recovery in the Mo circuit from the Cu concentrate can be assumed based on laboratory and plant scale tests [42]. An annual ore production of 36 Mt will give a production of 1047 tonnes MoS2 concentrate with 53% Mo, thus a Mo production of 544 tonnes/year. Together with a rough estimation of the rhenium content of the Aitik deposit based on the average rhenium concentration obtained in this study (213 ppm), the current reserve of the deposit (747 Mt), the MoS2 concentrate (1047 tonnes), and a general Re recovery (60%), it is obvious that these new products have the potential of increasing the value of the Aitik ore and extend the life of the mine. These are good examples demonstrating the importance of transforming qualitative and quantitative micro-scale information about the ore to a larger scale of direct importance for future production. By studying in-situ samples, the important link between analytical data from carefully chosen and examined samples to the character of specific rock volumes within the mine can be established, even if selective mining seldom is used in porphyry ores, information of this kind helps to improve predictions and mine planning.

Conclusions
Molybdenite in the Aitik area varies considerably in grain size, between the two studied ore bodies and within each ore body, and is dominantly very fine-grained. Most molybdenite grains are found as single grains, as aggregates, or intergrown with chalcopyrite, and are associated with late, post-ore geological features, such as overprinting garnet-magnetite-anhydrite-quartz-K feldspar-apatite-alteration, quartz-veining, and pegmatite dykes. The rhenium concentration of molybdenite varies considerably, with the higher concentrations obtained from Salmijärvi molybdenite samples. The large variation is probably the result of several magmatic/hydrothermal and metamorphic episodes that have been active in the region. The Aitik and Salmijärvi deposits exhibit similar molybdenum and rhenium contents as Mo-Re-producing porphyry Cu-Mo deposits worldwide (e.g., El Teniente and Chuiqicamata in Chile, and Bingham and Copper Creek in USA), and pilot plant tests have shown that recovery for molybdenum at Aitik is good compared to other deposits in the world. If molybdenum and rhenium circuits are installed, the price of molybdenum and rhenium in combination with the calculated amount of metal present in the Aitik ore body indicates that the two metals would constitute significant byproducts of copper production in Aitik. The data presented in this study describes the character and distribution of molybdenite in order to help predicting the outcome of this future large investment. The distribution, character, and rhenium concentration of molybdenite within the two investigated ore bodies seems to be related to specific alteration and vein features rather than to rock types, and these features also seem to have an impact on the final recovery of molybdenum. They are thus important to estimate quantitatively for processing and mine planning.