Discrimination of Mineralized Rock Types in a Copper-Rich Volcanogenic Massive Sulfide Deposit Through Fast Independent Component and Factor Analysis

Natural Resources Research - Multivariate methods are useful for simplifying the interpretation of variables in geochemical data and are widely used to uncover relationships between elements that...     

Mineral chemistry and petrogenesis of chromitites from the Khoy ophiolite complex,Northwestern Iran: Implications for aggregation of two ophiolites

The Khoy ophiolitic complex in Northwestern Iran is a part of the Tethyan ophiolite belt, and is divided into two sections: the Eastern ophiolite in Qeshlaq and Kalavanes (Jurassic–Cretaceous) and the Western ophiolite in Barajouk, Chuchak and Hessar (Late Cretaceous). Our chromitites can be clearly classified into two groups: high‐Al chromitites (Cr# = 0.38–0.44) from the Eastern ophiolite, and high‐Cr chromitites (Cr# = 0.54–0.72) from the Western ophiolite. The chromian spinels in high‐Al chromitite include primary mineral inclusions mainly as Na‐bearing diopside and pargasite with subordinate rutile and their formation was probably related to reaction between a MORB (mid‐ocean‐ridge basalt)‐like melt with depleted harzburgite, possibly in a back‐arc setting. Their host harzburgites contain clinopyroxene with higher contents of Al₂O₃, Na₂O, Cr₂O₃, and TiO₂ relative to Western harzburgites and are possibly residue after moderate partial melting (~15 %) whereas the Western harzburgite is residue after high partial melting (~25 %). The chromian spinel in the Western Khoy chromitites contains inclusions such as clinopyroxene, olivine and platinum group mineral‐bearing sulfides. These Western chromitites were possibly formed at two stages during arc growth and are divided into the moderately high‐Cr# chromitites (Barajouk and Hessar) and the high‐Cr# chromitites (Chuchak A and C). The former crystallized from island‐arc‐tholeiite (IAT) melts during reaction with the host depleted harzburgites, whereas the latter crystallized from boninitic melts (second stage melt) during reaction with highly depleted harzburgite in a supra‐subduction‐zone environment. Based on the mineral chemistry of chromian spinels, pyroxenes, and mineral inclusions, the chromitites and the host peridotites from the Eastern and Western Khoy ophiolites were formed in a back‐arc basin and arc‐related setting, respectively. The Khoy ophiolitic complex is a tectonic aggregate of the two different ophiolites formed in two different tectonic settings at different ages.     

The nature and origin of Fe-Ti-P-rich rocks in the Qareaghaj mafic-ultramafic intrusion, NW Iran

Summary Fe-Ti-P-rich rocks (FTP) are unusual with respect to their mineralogy and bulk composition. Varieties of these rocks are mostly related to Proterozoic massif-type anorthosites and to a lesser extent to the upper parts of mafic-ultramafic intracratonic layered complexes and other igneous rock suites. We present results on the geology, mineralogy and geochemistry of a new occurrence of FTP, associated with mafic rocks in the northwestern part of Iran. The Qareaghaj mafic-ultramafic intrusion (QMUI) is a small igneous body situated between Palaeozoic sedimentary rocks and a Precambrian low grade metamorphic complex. The QMUI is composed mainly of non-mineralized mafic and apatite- and Fe-Ti oxide-rich ultramafic rocks. The mafic rocks, mainly coarse-grained gabbro, microgabbro and amphibolite, have a simple mineral assemblage (plagioclase + clinopyroxene + ilmenite) and based on field observations, mineralogy and chemical composition are comagmatic. The ultramafic rocks with high proportion of olivine (∼40–66 vol.%), apatite (∼0.1–16 vol.%), ilmenite (∼11–19 vol.%) and magnetite (∼2–13 vol.%), have unusual bulk compositions (e.g., SiO₂ ∼ 21–30 wt.%, total iron expressed as Fe₂O₃ ^tot ∼ 26–42 wt.%, TiO₂ ∼ 5–11 wt.%, MgO ∼ 9–20 wt.%, P₂O₅ up to 5.1 wt.%, Cr ∼ 40–160 ppm, Ni ∼ 7–73 ppm). The FTP forms numerous sill-like layers, ranging in thickness from ∼5 cm to few meters. These rocks, totally enclosed in mafic rocks with sharp and concordant contacts, show a magmatic lamination and follow the general NW–SE trend of QMUI. The apatite-rich ultramafic rocks makes up 90–95% of the total ultramafic outcrops and contain Mg-poor olivine (Mg# ∼ 40–58) and low-Mg spinel (Mg# ∼ 30–44) in contrast to apatite-poor ones (∼60–63 and ∼43–46, respectively). Field relationships, mineral compositions and geochemical data suggested that the FTP are not related to the mafic host rocks. On the contrary, they intruded latter into the gabbros during plastic, high temperature deformation in local shear zones. Fractional crystallization of P-rich ferrobasaltic parental magma at depth, probably in an open magmatic system, not far from the QMUI magma chamber, is considered as responsible for the formation of the evolved FTP in QMUI.     

Triethylamine removal using biotrickling filter (BTF): effect of height and recirculation liquid rate on BTFs performance

This study investigated the removal of triethylamine using a biotrickling filter. The influence of affecting parameters, such as height and recirculation liquid rate (V _L) on contaminant removal efficiency, was examined in detail. The results demonstrated that in the constant empty bed residence time (EBRT), when V _L was increased, the removal efficiency (RE) increased. Also, for a specific V _L, increasing EBRT could also increase RE values. However, it seems that an increasing V _L is a more cost-effective way to enhance RE as compared to an increasing EBRT. The obtained outcomes represented that for a constant EBRT, an increase in inlet loading (IL) could decrease RE. For lower ILs, the removal of the contaminant could be carried out faster in height. The first part of the bed contributed the most to contaminant removal, and for the lower ILs, the contribution was even further. For the first section of bed in a constant IL, increasing EBRT could increase RE. In a constant IL and EBRT, increasing V _L could increase RE, as well as the removed mass loading by at least 20–25 g/m³/h. Also, the effect of the V _L increase on removal amount in the second and third sections of the bed was negligible.     

Effect of empty bed residence time on biotrickling filter performance: case study—triethylamine

In this study, a laboratory-scale biotrickling filter (BTF) is used to remove Triethylamine (TEA) from gaseous wastes. The BTF is made of stainless steel with a height of 210 cm and an internal diameter of 21 cm packed with lava rocks. TEA elimination pattern was evaluated by changing empty bed residence times (EBRTs). The maximum elimination capacity (EC) has been determined to be 87 g/m³/h. At all EBRTs 52, 31, 20, and 10 s, contaminant transferring from gas phase to liquid was more than the EC. Also, the removal efficiency was 100 % for a mass loading of 100 g/m³/h. While the liquid recirculation velocity of 3.466 m³/m²/h was maintained, the flow rate was adjusted to 60, 100, 156, and 312 L/min. The results show that due to the high solubility of TEA in water for all the EBRTs, TEA can be solved in the circulated liquid and then be degraded gradually by microorganisms. Therefore, the least EBRT of 10 s is more appropriate.