A comprehensive review on sustainable clay-based geopolymers for wastewater treatment: circular economy and future outlook.

In the present era of significant industrial development, the presence and dispersal of countless water contaminants in water bodies worldwide have rendered them unsuitable for various forms of life. Recently, the awareness of environmental sustainability for wastewater treatment has increased rapidly in quest of meeting the global water demand. Despite numerous conventional adsorbents on deck, exploring low-cost and efficient adsorbents is interesting. Clays and clays-based geopolymers are intensively used as natural, alternative, and promising adsorbents to meet the goals for combating climate change and providing low carbon, heat, and power. In this narrative work, the present review highlights the persistence of some inorganic/organic water pollutants in aquatic bodies. Moreover, it comprehensively summarizes the advancement in the strategies associated with synthesizing clays and their based geopolymers, characterization techniques, and applications in water treatment. Furthermore, the critical challenges, opportunities, and future prospective regarding the circular economy are additionally outlined. This review expounded on the ongoing research studies for leveraging these eco-friendly materials to address water decontamination. The adsorption mechanisms of clays-based geopolymers are successfully presented. Therefore, the present review is believed to deepen insights into wastewater treatment using clays and clays-based geopolymers as a groundbreaking aspect in accord with the waste-to-wealth concept toward broader sustainable development goals.

Evaluation insight into Abu Zenima clay deposits as a prospective raw material source for ceramics industry: Remote Sensing and Characterization.

The rapid development and mutations have heightened ceramic industrialization to supply the countries' requirements worldwide. Therefore, the continuous exploration for new reserves of possible ceramic-raw materials is needed to overwhelm the increased demand for ceramic industries. In this study, the suitability assessment of potential applications for Upper Cretaceous (Santonian) clay deposits at Abu Zenima area, as raw materials in ceramic industries, was extensively performed. Remote sensing data were employed to map the Kaolinite-bearing formation as well as determine the additional occurrences of clay reserves in the studied area. In this context, ten representative clayey materials from the Matulla Formation were sampled and examined for their mineralogical, geochemical, morphological, physical, thermal, and plasticity characteristics. The mineralogical and chemical compositions of starting clay materials were examined. The physicochemical surface properties of the studied clay were studied utilizing SEM-EDX and TEM. The particle-size analysis confirmed the adequate characteristics of samples for white ceramic stoneware and ceramic tiles manufacturing. The technological and suitability properties of investigated clay deposits proved the industrial appropriateness of Abu Zenima clay as a potential ceramic raw material for various ceramic products. The existence of high kaolin reserves in the studied area with reasonable quality and quantity has regional significance. It would significantly help reduce the manufacturing cost and overwhelm the high consumption rate. The ceramic manufacturers in the investigated areas are expected to bring steady producers into the industry in the long term to gain the advantage of low-cost raw materials, labor, and factory construction.

Integrating mineralogy, geochemistry and aeromagnetic data for detecting Fe-Ti ore deposits bearing layered mafic intrusion, Akab El-Negum, Eastern Desert, Egypt.

This study delineated the Fe-Ti oxide deposit concurrencies on the layered mafic intrusion in Gabal Akab El-Negum (GAN), South Eastern Desert, Egypt, using aeromagnetic mapping and chemical analysis of the hosted mafic rocks and mineralogical studies. Aeromagnetic data was improved using the enhanced horizontal gradient amplitudeto detect the primary structures (edges/contacts/faults) that control the distribution of Fe-Ti ore deposit. GAN layered gabbros are differentiated into troctolite, olivine-, pyroxene-, and hornblende-gabbros. These mafic rocks primarily comprise plagioclase, olivine, pyroxene, and hornblende with Fe-Ti ores (magnetite and ilmenite). The significant variation in Mg# of clinopyroxene between 0.70 and 0.82 indicates the importance of fractional crystallization in developing layered mafic intrusion. Clinopyroxene and plagioclase thermometry yielded low temperatures similar to the fractionated primary basaltic magma. The pairs of magnetite-ilmenite minerals in gabbros provide equilibrium temperatures of 539.44-815.56, and high fO2, reflecting various cooling and subsolidus reequilibration phases of minerals. The enrichment of GAN gabbros in light rare-earth elements relative to heavy rare-earth elements indicates the interaction between the Fe-Ti rich mantle and the fractionated tholeiitic magmas in the back-arc setting, generating Fe-Ti oxide ores.

Characterization of activated bentonite clay mineral and the mechanisms underlying its sorption for ciprofloxacin from aqueous solution.

The presence of emerging pollutants such as hazardous chemicals, pharmaceuticals, pesticides, and endocrine-disrupting chemicals in water sources is a serious concern to the environment and human health. Thus, this study focused on exploring the interaction mechanisms between ciprofloxacin (CIP) (antibiotic) and clay (a low-cost adsorbent) during sorption process. Acid activation technique was opted for modifying natural bentonite (NB) to enhance the adsorptive removal of CIP from water. The BET surface area analysis revealed that acid-activated bentonite (AAB) possessed more than two fold higher surface area as compared to NB. Combining pHzpc measurements, effect of solution pH and CIP speciation revealed that CIP sorption onto bentonite is highly dependent on solution pH. Kinetic studies confirmed that CIP sorption mechanism was chemisorption which included ion-exchange and surface complexation mechanisms. The mechanism of CIP sorption onto AAB was successfully explored with the assistance of characterization techniques. Maximal monolayer sorption capacity of AAB was found to be 305.20 mg/g, compared to 126.56 mg/g for NB. Reusability studies demonstrated that AAB could be reused successfully up to 5 cycles. Furthermore, column studies showed satisfactory results confirming that AAB can be successfully used in continuous mode for practical applications.

Tuning tetracycline removal from aqueous solution onto activated 2:1 layered clay mineral: Characterization, sorption and mechanistic studies.

Water pollution due to emerging contaminants (especially pharmaceuticals) is a major environmental threat which results in the development of antibiotic-resistant bacteria/resistance genes in the aquatic environment. Therefore, robust and cost-effective methods are required to address this problem. In this study, thermal activation was opted for the modification of natural bentonite clay (BC) and utilized to investigate the adsorptive removal of tetracycline (TC) from aqueous solution. The physicochemical surface properties of the raw and modified bentonite samples were also investigated. The BET analysis revealed that the thermally activated bentonite (TB) has better properties than BC. The surface area of TB was found to be more than two-fold higher compared to that of BC. The FTIR spectra exhibited the existence of AlOH, SiO and SiOSi functional groups in the samples, confirming the presence of hydrated aluminosilicate in the clay. The effects of various operating parameters were analyzed via optimization studies. The maximum monolayer adsorption capacity estimated by Langmuir model was found to be 156.7 and 388.1 mg g-1 for BC and TB, respectively. Furthermore, fixed-bed column studies were performed to get insights into the adsorption behavior of TB in a dynamic system. The mechanism of TC adsorption by TB was successfully explored.

Enhanced interlayer trapping of Pb(II) ions within kaolinite layers: intercalation, characterization, and sorption studies.

Lead (Pb(II)) pollution in water poses a serious threat to human health in many parts of the world. In the past decades, research has been aimed at developing efficient and cost-effective methods to address the problem. In this study, dimethyl sulfoxide (DMSO) and potassium acetate (K-Ac) intercalated kaolinite complexes were synthesized and subsequently utilized for Pb(II) removal from water. The intercalation of kaolinite with DMSO was found to be useful for expanding the interlayer space of the clay mineral from 0.72 to 1.12 nm. Kaolinite intercalation with K-Ac (KDK) increased the interlayer space from 1.12 to 1.43 nm. The surface area of KDK was found to be more than threefold higher as compared to natural kaolinite (NK). Batch experimental results revealed that the maximum Pb(II) uptake capacity of KDK was 46.45 mg g-1 which was higher than the capacity of NK (15.52 mg g-1). Reusability studies showed that KDK could be reused for 5 cycles without substantially losing its adsorption capacity. Furthermore, fixed-bed column tests confirmed the suitability of KDK in continuous mode for Pb(II) removal. Successful application of intercalated kaolinite for Pb(II) adsorption in batch and column modes suggests its application in water treatment (especially removal of divalent metals).

The interaction of heavy metals and metalloids in the soil-plant system in the São Domingos mining area (Iberian Pyrite Belt, Portugal).

São Domingos belongs among the most important historic Iberian Pyrite Belt Cu mines. The anthrosoil is contaminated by a very high content of heavy metals and metalloids. The study was focused on evaluating the interaction of some chemical elements (Ca, Mg, Fe, Mn, Cu, Pb, Zn, Ag, Cd, Ni, Co, As, Sb) in the system soil vs. five autochthonous dominant plant species: Pinus pinaster Aiton, Quercus rotundifolia Lam., Agrostis sp., Juncus conglomeratus L. and Juncus effusus L. The plants are heavily contaminated by Cu, Pb, As and Zn. The bioconcentration factor proved that they exhibit features of metal tolerant excluders. The trees are accumulators of Ag, whereas the graminoids are hyper-accumulators of Ag and Juncus effusus of Co. The translocation factor confirmed that the selected elements are immobilised in the roots except for Mn and Zn in Pinus pinaster and Mn in Quercus rotundifolia and Juncus conglomeratus. The bioaccumulation of Mn, Zn and Cu at low pH increases. The increased content of Ca and Mg in the soil inhibits, in the case of some metals and metalloids, their intake to plants. Although the studied plants, despite their fitness and vitality at the contaminated sites, are not suitable for phytoextraction (except Co and Ag), they can be used for phytostabilisation at the mining habitats.

Raman spectra of oriented and non-oriented Cu hydroxy-phosphate minerals: libethenite, cornetite, pseudomalachite, reichenbachite and ludjibaite.

Oriented cornetite [Cu3PO4(OH)3], libethenite [Cu2PO4(OH)] and pseudomalachite [Cu5(PO4)2(OH)4] and non-oriented reichenbachite [Cu5(PO4)2(OH)4] and ludjibaite [Cu5(PO4)2(OH)4] minerals from Lubietová and Spania Dolina dump fields, Banská Bystrica, Slovakia were examined by polarized Raman spectroscopy. The examined minerals display the characteristic vibrational modes of PO4 and OH groups and further lattice modes. The PO4 stretching and bending vibrations of the investigated minerals occur between 1150 and 900 cm(-1) and between 700 and 350 cm(-1), respectively. On the other hand, the hydroxyl group stretching and bending modes appear above 3350 cm(-1) and between 900 and 700 cm(-1), respectively. The lattice vibrations occur below 350 cm(-1). The different bond distances of the PO4 groups readily explain the shift of the bands to higher or lower wavenumbers among the studied Cu hydroxy-phosphate minerals.