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This article presents, for the first time, the study of diabases from various ophiolite complexes from Greece and Cyprus to identify their performance as concrete aggregates. Within this scope, in the first step, diabase samples from four selected ophiolite complexes of Greece (Veria-Naousa, Edessa and Guevgueli) and Cyprus (Troodos) were collected in order to estimate their suitability as concrete aggregates by means of their petrographic and physicochemical characteristics. In the next step, concrete specimens were prepared and their mechanical strength was measured in order to investigate their mechanical performance. Additionally, their petrographic characteristics in relation to the mechanical strength of the created concretes were investigated for the first time. Concrete specimens prepared by employing diabases from the Veria-Naousa and Guevgueli complexes as aggregates were reckoned as the most durable ones in contrast to those derived from the Edesssa complex and even more so than those from Cyprus, with the latter containing the most altered diabases (rodingitised). The overall conclusion of this research is that the engineering properties of the aggregates were dependent on their petrographic characteristics and hence they influenced the final mechanical behaviour of each produced concrete. [ABSTRACT FROM AUTHOR]

This study investigates the capability of the Southeast Mesohellenic Trough (SE MHT) sandstone formations to serve as a potential reservoir for CO2 storage in response to the emerging climate change issues by promoting environmentally friendly mineral sequestration applications. Sandstone samples, for the first time, were evaluated for their petrographic characteristics, mineral chemistry, geochemical properties, as well as their petrophysical and gas adsorption properties through tests. The sandstones were tested and classified into distinct groups. The most promising site to be considered for pilot CO2 storage testing is the Pentalofos Formation locality since its sandstones display specific mineral phases with the proper modal composition to conceivably react with injected CO2, leading to the development of newly formed and stable secondary mineral phases. The gas adsorption results are also more encouraging for sandstones from this sedimentary formation. All the measured UCS (uniaxial compressive strength), Ei (bending stiffness), and ν (Poisson's ratio) results are above those dictated by international standards to perform CO2 storage practices safely. Furthermore, the specified targeted locality from the Pentalofos Formation holds the geological advantage of being overlaid by an impermeable cap-rock formation, making it suitable for deploying CO2 mineralization practices. The demarcated area could permanently store a calculated amount of ~50 × 105 tons of CO2 within the geological reservoir by reacting with the specified mineral phases, as specified through the proposed petrographic PrP index (potential reactive phases). [ABSTRACT FROM AUTHOR]

In the Aegean region (Cyclades – Greece), a large part of the Island of Anafi consists of exhumed high-grade metamorphic sequences (amphibolites, serpentinites and metasediments) that have been intruded by Late Cretaceous intermediate and felsic granitoids. These correspond to I-type arc-related rocks, displaying calc-alkaline geochemical affinities. Variability in their petrographic features, mineral composition and geochemistry is assigned to differentiation processes that mostly involved plagioclase and/or K-feldspar, and to a lesser extent amphibole and biotite. Mineral chemistry and geochemical results suggest that the Anafi granitoids are highly comparable with the Late Cretaceous granitoid intrusive rocks from East Crete and Donousa island. The amphibole and zircon saturation thermometry yields relatively moderate temperature crystallization conditions (~790°C) for the intermediate granitoids and lower for the felsic granitoids (~630°C). Geobarometric calculations based upon the chemistry of magnesiohornblende, as well as the normative (Qz), (Ab) and (Or) contents clearly point to shallow intrusion conditions (~2.0–6.5 kbar), corresponding to an estimated depth of crystallization of ~12 ± 4 km. The thrust sheets that overly the Palaeogene flysch in Anafi (metasediments with serpentinized peridotites, amphibolites and metabasites), constitute a subducted and metamorphosed oceanic sequence. These metamorphic units likely represent a part of the Pindos – Cycladic Blueschist Unit domain that was subducted at an earlier pre-Campanian stage. In the hydrated mantle wedge, incorporation of shallow level granitoids within metamorphic units was likely facilitated via corner flow intrusion mechanisms. Following the intrusion, the granitoid rocks were exhumed in a syn-convergent setting, along with the metamorphic thrust sheets, by continuous underplating of more external units, thus, escaping penetrative ductile deformation. [ABSTRACT FROM AUTHOR]

Large ultramafic bodies of the East Othris ophiolite in Central Greece consist of serpentinites, of harzburgite precursors, as well as serpentinized lherzolites, which have been intruded by thin dykes of olivine-rich and olivine-poor pyroxenites. They represent parts of partially altered upper mantle wedge rocks in a Mid-Late Jurassic intraoceanic subduction setting of the Pindos microocean, a western strand of the Tethyan oceanic realm. Serpentinization and rodingitization occurred during their exhumation toward the fore-arc oceanic region and accretionary prism through a subduction channel. Petrography and geochemistry show that protoliths of most serpentinites and serpentinized peridotites are harzburgites, while few are more fertile lherzolites. Petrogenetic modeling reveals that the former harzburgites correspond to highly depleted residual mantle peridotites, which formed after moderate degrees (~13-20 %) of hydrous partial melting, whereas lherzolites, being closely related to the ophiolitic mantle peridotites of West Othris, resulted after lower partial melting degrees (~7-10 %). Mineral chemistry and geochemical data from pyroxenites imply that they have been derived after crystallization of a subduction-related IAT hydrous magma that formed after moderate partial melting degrees (~14-19 %), quite similar to those that produced the harzburgites. Melting processes for the East Othris mantle peridotites occurred in the spinel-stability field, at estimated equilibrium temperatures ranging between 900 and 1,050 °C and pressures between 1.4 and 1.7 GPa, in a rather highly oxidized environment. It is estimated that the primary IAT magma, formed under relatively high temperatures with liquidus temperature at ~1,260 °C and mantle potential temperature at ~1,372 °C. Cooling rates of the shallow mantle beneath the Pindos oceanic basin, from its Mid-Triassic rift/drift phase and the subsequently developed Mid-Late Triassic short-lived intraoceanic subduction, to the Mid-Late Jurassic main subduction phase, are estimated at ~0.7 and ~1.6 °C/Ma, respectively, with the latter being considered as unusually high. [ABSTRACT FROM AUTHOR]

In the Veria-Naousa ophiolitic complex (north Greece), rodingite appears mainly in the form of cross cutting dykes within serpentinised peridotites. It is distinguished into three types, based upon the provenance of its protoliths, textural characteristics, mineralogical assemblages and geochemical affinities. Type I rodigites were derived from boninitic diabasic protoliths and their mineralogical assemblage include garnet + clinopyroxene + chlorite. Type II rodingites were formed at the expense of gabbroic precursors, comprising clinopyroxene + garnet + vesuvianite ± quartz, whereas Type III rodingites replaced diabasic tholeiitic protoliths comprising of garnets + vesuvianite + clinopyroxene + chlorite. Rodingitisation resulted in desilification, decrease of alkalies, Al, Fe, Mg and increase in Ca contents. In Type I rodingites the MREE (middle rare earth elements) and HREE (heavy rare earth elements) were slightly reduced. Type II rodingites experienced LREE (light rare earth elements) depletions, whereas MREE and HREE remained fairly stable. Restricted mobility of REE in Type III rodingites is assigned to shallow-level rodingitisation under decreasing pH. Rodingitisation occured in two distinct stages at fore-arc settings. The first stage occured under mildly oxidising conditions and enhanced CO 2 /H 2 O ratios. This stage affected the protoliths of all rodingite types. The second rodingitisation stage occured under more oxidising conditions and lower CO 2 /H 2 O ratios, which corresponds to the exhumation stage of the serpentinite-rodingite formations. Types II and III rodingites were subjected to further rodingitisation under the increasing influence of slab-derived hydrous phases at shallower depths, leading to the formation of late-stage andradite and vesuvianite. All stages of rodingitisation are estimated to have occurred under relatively moderate temperatures and pressure (~300 to 450 °C; ~2–6 kbar respectively). • Three distinct types of rodingites have been identified in Veria-Naousa ophiolitic complex • Boninitic diabases, gabbros and tholeiitic diabases served as the protoliths • Garnet, clinopyroxene, chlorite and vesuvianite are the main rodingite mineral phases • Low CO 2 /H 2 O ratios and temperature conditions promoted andradite's & vesuvianite's formation at the final exhumation stages [ABSTRACT FROM AUTHOR]

The partly to pervasively metasomatized doleritic and gabbroic dykes or small to medium sized bodies found in East Othris, within Mid to Late Jurassic serpentinized peridotites of ophiolitic units and ophiolitic mélange formations are classified as rodingites and can be divided into two types. Type 1 rodingites are mainly characterized by the frequent occurrence of prehnite, while Type 2 rodingites include mostly garnets and vesuvianite. Isocon analysis showed that rodingitization essentially occurred with mass and volume preservation. Desilification, depletion of alkalies, as well as Ca enrichment was more intense for the Type 2 rodingites. Al, Fe and Mg remained rather immobile, while Ti, Y, Zr and REE were variably depleted. Rodingitization took place in an intraoceanic subduction system. It occurred in three successive stages during the exhumation of the mafic–ultramafic mantle wedge rocks in a fore-arc setting within a serpentinitic subduction channel, which developed close to the slab. The incorporation of the mafic rocks to the subduction channel probably resulted after entraining a directed mantle flow towards the slab. The first stage of rodingitization formed mainly grossular, hydrogrossular, Ti- and Cr-bearing hydrogarnets and calcite under relatively acidic and mildly oxidizing physicochemical conditions, with increased CO2/H2O ratio. During the second and more extensive rodingitization stage, alkaline and reducing conditions prevailed and CO2/H2O ratio was decreased. The modeling of the mineral reactions of this stage, using the software winTWQ v. 2.34 in the CFMASH system, reveals that in Type 1 rocks prehnite replaced most of the initial garnet, while Type 2 rocks continued to be rodingitized, mostly forming grossular and/or hydrogrossular and chlorite. Hydrogrossular, instead of grossular, was crystallized from hydrous fluids under high silica activity. Type 2 rodingites underwent further rodingitization during the third stage, due to infiltration of Ca-rich hydrothermal fluids of oceanic and/or subducted slab origin, at lower temperatures and depths. This stage is characterized by the appearance of hydroandradite and vesuvianite, under alkaline and oxidizing conditions, due to very low CO2/H2O ratio and relatively high fO2. All three rodingitization stages are estimated to have occurred under relatively moderate temperature and pressure (~300 to 400°C; ~3–6kbar respectively). Locally, Type 2 rodingites show derodingitization of variable extent, forming high-variance assemblages mostly consisting of chlorite±pumpellyite. Some chlorite marginal zones in rodingite dykes may also have been developed by Mg-rich diffusional fluid flow, during this derodingitization process. [ABSTRACT FROM AUTHOR]

East Othris area consists of scattered ophiolitic units, as well as ophiolitic mélange occurrences, which encompass gabbroic rocks. These rocks have been affected by low-grade ocean floor metamorphism ( T < 350°C and P < 8 kbar). Based on their petrography, mineral chemistry and geochemistry gabbroic rocks have been distinguished into gabbros and diorites, with the latter being divided into two groups. Gabbros seem to have been formed from moderate to high partial melting degrees (~8-25%) of a highly depleted mantle source, while group (1) diorites have been differentiated after variable fractionation processes (up to 30%). Group (2) diorites seem to have been derived from low partial melting degrees (~3%) of a fertile or moderately depleted mantle source and with extensive fractionation processes (~50%). Geochemical results suggest that partial melting processes occurred at relatively shallow depths, in the plagioclase-spinel stability field, while amphibole chemistry data indicate shallow level crystallization. Chondrite and PM-normalized patterns, Th/Yb, and Nb/Th ratios as well as mineral chemistry analyses show that gabbros and group (1) diorites (with relatively low PM-normalized Nb and Ta values and negative Ti anomalies) suggest subduction processes, while group (2) diorites are MORB or BAB related. Some gabbros have been characterised as high-Mg, being compositionally similar to picrites or boninites. Variability in extent of partial melting of the mantle source and the different geotectonic environment affinities are consistent with a supra-subduction zone (SSZ) origin of the east Othris ophiolites. The fact that IAT related rocks are more abundant in east rather than in west Othris may possibly be explained by a slab rollback model retreating to the east within the Pindos oceanic basin. [ABSTRACT FROM AUTHOR]

In West Macedonia (Greece), CO2 accounts as one of the largest contributors of greenhouse gas emissions related to the activity of the regional coal power plants located in Ptolemaida. The necessity to mitigate CO2 emissions to prevent climate change under the Paris Agreement's framework remains an ongoing and demanding challenge. It requires implementing crucial environmentally sustainable technologies to provide balanced solutions between the short-term needs for dependency on fossil fuels and the requirements to move towards the energy transition era. The challenge to utilise and store CO2 emissions will require actions aiming to contribute to a Europe-wide CCUS infrastructure. The Horizon 2020 European Project "STRATEGY CCUS "examines the potential for CO2 storage in the Mesohellenic Trough from past available data deploying the USDOE methodology. Research results show that CO2 storage capacities for the Pentalofos and Eptachori geological formations of the Mesohellenic Trough are estimated at 1.02 and 0.13 Gt, respectively, thus providing the potential for the implementation of a promising method for reducing CO2 emissions in Greece. A certain storage potential also applies to the Grevena sub-basin, offering the opportunity to store any captured CO2 in the area, including other remote regions. [ABSTRACT FROM AUTHOR]

Triassic rift-related volcanic rocks outcrop over all mainland Greece, comprising of trachybasalts and basaltic trachyandesites. Relatively immobile to the effects of alteration processes major and trace element abundances classify the volcanics into OIB and E -MORB lavas. They have mainly been distinguished based upon their: i) LREE contents, ii) silica-saturation index (S·I.), iii) Zr/Nb and Nb/Y ratio values; iv) Th, U, and Ta contents v) geotectonic discrimination diagrams. Their geochemistry indicates that most rocks were affected by moderate to extensive differentiation processes, mostly expressed by clinopyroxene fractionation. Some of the OIB and E -MORB volcanics are considered as primitive undersaturated, displaying (low SiO 2 , Zr/Nb and S.I. values, enhanced CaO/Al 2 O 3 ratios). Calculated average mantle potential temperatures are comparable (1410 °C OIB; 1370 °C E -MORB), with melt fractions estimated at 3–5% for primary OIB magmas and 6–8% for primary E -MORB magmas. An asthenospheric origin is inferred for the OIB lavas, with melting in the garnet stability field (75–95 km; 2.5–3.0 GPa), whereas E-MORB parent magmas were formed with melting in the garnet/spinel (transitional) stability field (55–70 km; 1.8–2.2 GPa). The Hellenic Triassic rift-related lavas were most likely generated and erupted after lithospheric attenuation and extension, followed by subsequent asthenospheric upwelling of the mantle. The high calculated partial melting degrees and the observed thick and voluminous lava formations account for fast-spreading of the Tethys ridge during the Triassic. Temperature results suggest that the Hellenic Triassic rift-related magmas were generated from mantle at ambient temperature, render a mantle plume-based scenario improbable. • Mantle potential temperatures are estimated at 1370–1410 °C with 3–8% melt fractions. • OIB lavas were generated at 75–95 km and E-MORB at 55–70 km depth. • A mantle plume-based scenario is not favoured. [ABSTRACT FROM AUTHOR]

Greece is considered amongst the world's top marble producers in the global carbonate ornamental stone market. Selected Greek carbonate ornamental stones considered in our study suite are characterized by their distinctive and in some cases unique appearance, having a significant impact on their commercial value. Their wide range of colour varieties and their physico-mechanical properties are closely related to their mineral assemblage, chemical constitution, petrographic properties, structural defects, which in turn depend highly upon their metamorphic/diagenetic grade and in some cases hydrothermal processes that affected them. This study endeavors to feature the petrographic, mineralogical and geochemical properties of the main Greek carbonate ornamental stones from selected localities and their by-product waste material used as aggregates. The documented data aims to serve a better understanding of the dynamic Greek marble industry by relating their mineral and chemical properties with their physico-mechanical and aesthetic characteristics. [ABSTRACT FROM AUTHOR]

Underground geological energy and CO2 storage contribute to mitigation of anthropogenic greenhouse-gas emissions and climate change effects. The present study aims to present specific underground energy and CO2 storage sites in Greece. Thermal capacity calculations from twenty-two studied aquifers (4 × 10−4–25 × 10−3 MJ) indicate that those of Mesohellenic Trough (Northwest Greece), Western Thessaloniki basin and Botsara flysch (Northwestern Greece) exhibit the best performance. Heat capacity was investigated in fourteen aquifers (throughout North and South Greece) and three abandoned mines of Central Greece. Results indicate that aquifers present higher average total heat energy values (up to ~6.05 × 106 MWh(th)), whereas abandoned mines present significantly higher average area heat energy contents (up to ~5.44 × 106 MWh(th)). Estimations indicate that the Sappes, Serres and Komotini aquifers could cover the space heating energy consumption of East Macedonia-Thrace region. Underground gas storage was investigated in eight aquifers, four gas fields and three evaporite sites. Results indicate that Prinos and South Kavala gas fields (North Greece) could cover the electricity needs of households in East Macedonia and Thrace regions. Hydrogen storage capacity of Corfu and Kefalonia islands is 53,200 MWh(e). These values could cover the electricity needs of 6770 households in the Ionian islands. Petrographical and mineralogical studies of sandstone samples from the Mesohellenic Trough and Volos basalts (Central Greece) indicate that they could serve as potential sites for CO2 storage. [ABSTRACT FROM AUTHOR]

This study investigates how the petrographic features of Klepa Nafpaktias sandstones affect their behavior in construction applications such as concrete, in environmental applications such as energy storage as well as whether they are suitable for the above uses. For achieving this goal, sandstones (ten samples) were collected in order to study their petrographic characteristics using petrographic microscope and GIS software, as well as their basic physical, mechanical and physicochemical properties were also examined. Concrete specimens (C25/30) were made according to international standards including the investigated aggregate rocks in various grain sizes. Various sandstones were tested and classified in three district groups according to their physicomechanical features as well as to their petrographic and microtopographic characteristics. Concrete strength's results determined the samples into three groups which are in accordance with their initial classification which was relative to their grain size (coarse to fine-grained). As the grain size decreases their physicomechanical and physicochemical properties get better resulting in higher concrete strength values (25 to 32 MPa). Furthermore, the proposed ratio C/A (crystals/mm2) seems to influence the aggregate properties which constitute critical factors for the final concrete strength, presenting the more fine-grained sandstones as the most suitable for concrete aggregates. Concerning the use of Klepa Nafpaktias sandstones as potential energy reservoirs, the studied sandstones presented as suitable for CO2 storage according to their physicomechanical characteristics. [ABSTRACT FROM AUTHOR]

Cumulate wehrlites, ultramafic lavas, and associated mafic dykes and pillow-lavas outcropwithin a Middle-Late Triassic igneous and sedimentary sequence in Othris, Central Greece.These rocks have been variably affected by metasomatic and metamorphic processes.Ultramafic rocks (wehrlites and ultramafic lavas) are serpentinized in processes thatare restricted (moderate alteration) or pervasive, forming serpentinites. Balancedlizardite/antigorite ratios suggest that serpentinization took place under conditions thatreached greenschist facies. Most trace element concentrations were relatively decreasedduring serpentinization. Local rodingitization is characterized by the formation ofhydrogarnets, secondary diopside, chlorite, pumpellyite and prehnite. This metasomaticmineral assemblage replaced cumulus clinopyroxene as well as primary accessoryplagioclase. Rodingitization occurred with diffusive mass transfer of CaOH+ species underrelatively mildly oxidizing physicochemical conditions, along with fluid solutions with anincreased CO2/H2O ratio. Rodingites formed as a result of extensive metasomatism that replaced protolithicboninitic dykes intruding wehrlites. The metasomatic hydrous fluids responsible for thisprocess were relatively alkaline, occurring under low to moderate P-T conditions (180-320 ˚C, P≈2-5 kbar), in conditions of increased fO2. Rodingites experienced desilification, androdingitization also resulted in variable decreases and less often increases in trace elementconcentration. Carbonation processes affected ultramafic lavas; the most intense carbonation is exposedin the Neraida locality where it has created "layer-cake" structures within the lavas.Metasomatic carbonation was caused by shallow-level continuous circulation of Ca-richfluids too low in temperature to significantly affect clinopyroxenes. The restrictedoccurrence of serpentine and hydroandradite indicates that carbonation occurred inassociation with low-grade serpentinization and rodingitization processes. Themetasomatic phenomena documented herein are related to subduction settings and morespecifically to the seafloor exhumation of the mafic–ultramafic rocks in the fore-arcarea. We have calculated that serpentinization and rodingitization of wehrlites began withinrelatively moderate temperature and pressure conditions (∼350 ˚ C, P≈6 kbar), withrodingitization processes in both wehrlites and rodingites progressing during furthercontinuous cooling of circulating hydrothermal fluids at shallower depths. The finalmetasomatic stage is represented by carbonation processes. Reference: Koutsovitis, P., Magganas, A., Ntaflos, T., Koukouzas N. 2018.Rodingitization and carbonation, associated with serpentinization of Triassic ultramaficcumulates and lavas in Othris, Greece. Lithos, 320-321, 35-48. [ABSTRACT FROM AUTHOR]

[Display omitted] • High-Cr podiform chromitites were produced from boninitic melts. • Boninitic melts transported via dunite pathways within a highly depleted mantle. • Consistent with PGE geochemistry, the reported PGM belong to the Os-Ir-Ru system. • Magmatic laurite's extensive solid solution series is attributed to melt cooling. • Cr-ore and PGM genesis occurred below the Moho in the fore-arc. Podiform chromitites of the Vavdos ophiolite are associated with dunite bodies hosted within residual mantle harzburgite. The mantle source is highly depleted and apparently developed at fore-arc settings as inferred from the presence of boninitic melts. The ascendance of these melts through dunite pathways and their subsequent interaction with the depleted harzburgite instigated chromitite mineralization within dunite. Spinel occurs in a) massive accumulations (Mg# = 0.56–0.68 and Cr# = 0.69–0.77), b) in non-massive disseminated textures (Mg# = 0.52–0.61 and Cr# = 0.80–0.81) and c) in schlieren chromitite deposits within dunite bodies (Mg# = 0.43–0.48 and Cr# = 0.79–0.82). Olivine is the main silicate inclusion in chromitites, whereas the absence of hydrous mineral phases is linked with crystallization at relatively deeper parts of the mantle. Olivine inclusions in spinel are enriched in Fo, Ni and Ca compared to the interstitial olivine grains. No compositional gaps were noted between the mineral analyses of chromitites and dunites; the calculated parental melts are also homogeneous, reinforcing the view for production of melt batches by similar processes. Platinum-group elements (PGE) concentrations and platinum-group minerals (PGM) demonstrate high (Os + Ir + Ru)/ (Rh + Pt + Pd) ratios, typical of many Tethyan ophiolitic chromitites. The main PGM phase is laurite that forms an extended solid solution series with substitution of Ru for Os + Ir, linked to the cooling of the system. Massive chromitites contain Ru-rich laurite and Os-Ir alloys whereas non-massive ores contain Ru-poor laurite. The PGM were included in fresh magnesiochromite favoring their magmatic origin and initial entrapment at ~ 1200 °C and low sulfur fugacity. [ABSTRACT FROM AUTHOR]

Various types of plutonic and volcanic rocks and their alteration products from Greece (serpentinite, magnesite and andesite), have been used for sustainable removal of Uranium (U) from the acidic drainage of Kirki mine, as well as for the pH increase of the polluted solutions. In this light, this study aims at the further understanding and improvement of the ecofriendly reuse of sterile, natural raw materials (including those remaining through industrial processing and engineering testing of aggregate rocks), for remediation of acid mine drainage. The selected rocks constitute such residues of sterile materials were used as filters in experimental continuous flow devices in the form of batch-type columns, in order to investigate acidic remediation properties with special focus on U removal. The initial pH of the wastewater was 2.90 and increased after seven (7) days of experimental application and more specifically from the fourth day onwards. Uranium removal became quantitatively significant once pH reached the value of 5.09. The volcanic rocks appeared to be more effective for U removal than the plutonic ones because of microtextural differences. However, optimum U removal was mainly achieved by serpentinite: while the raw materials rich in Mg strongly reacted and remediated the pH of the drainage water waste. Furthermore, the increase of pH values due to the presence of mineral raw materials, provided increased oxidation potential which deactivated the toxic load of metals, particularly U. Consequently, batch-type serpentinite reaction with the tailing fluid caused a drop in U concentration from an initial value of 254 ppb to the one of 8 ppb, which corresponds to 97% of removal. Andesite presented the second best reactant for experimental remediation, especially when it was mixed with magnetically separated mineral fractions. Despite the fact that the proposed methodology is currently at a relatively low Technology Readiness Level (TRL), it carries the potential to become an extremely effective and low-cost alternative to conventional environmental restoration technologies. • Filters of mineral raw materials to remove uranium from acidic drainage. • Serpentinite opaque minerals are proved to be the most effective for U removal. • The proposed methodology is extremely effective and a low-cost one. • Key role for the eco-friendly U removals is mineral raw material's microstructure. [ABSTRACT FROM AUTHOR]