Assessment of chromite ore wastes for methylene blue adsorption: Isotherm, kinetic, thermodynamic studies, ANN, and statistical physics modeling.

This research investigates the adsorption potential of chrysotile and lizardite, two minerals derived from chromite ore wastes, for the uptake of Methylene Blue (MB) dye from waste streams. The characterization of these minerals involves XRD, XRF, FTIR, and SEM. Results confirm the dominance of polymorphic magnesium silicate minerals, specifically chrysotile and lizardite, in the samples. The FTIR spectra reveal characteristic vibration bands confirming the presence of these minerals. The SEM analysis depicts irregular surfaces with broken and bent edges, suggesting favorable morphologies for adsorption. N2 adsorption-desorption isotherms indicate mesoporous structures with Type IV pores in both adsorbents. The Central Composite Design approach is employed to optimize MB adsorption conditions, revealing the significance of contact time, adsorbent mass, and initial MB concentration. The proposed models exhibit high significance, with F-values and low p-values indicating the importance of the studied factors. Experimental validation confirms the accuracy of the models, and the optimum conditions for MB adsorption are determined. The influence of solution acidity on MB uptake is investigated, showing a significant enhancement at higher pH values. Isothermal studies indicate Langmuir and Freundlich models as suitable descriptions for MB adsorption onto chrysotile and lizardite. The maximum adsorption capacities of MB for chrysotile and lizardite were found to be 352.97 and 254.85, respectively. Kinetic studies reveal that the pseudo-first-order model best describes the adsorption process. Thermodynamic analysis suggests an exothermic and spontaneous process. Statistical physics models further elucidate the monolayer nature of adsorption. Additionally, an artificial neural network is developed, exhibiting high predictive capability during training and testing stages. The reusability of chrysotile and lizardite is demonstrated through multiple regeneration cycles, maintaining substantial adsorption potential. Therefore, this research provides comprehensive insights into the adsorption characteristics of chrysotile and lizardite, emphasizing their potential as effiective and reusable sorbents for MB uptake from wastewater.

A New Perspective on Adsorbent Materials Based Impregnated MgSiO3 with Crown Ethers for Palladium Recovery.

The study of new useful, efficient and selective structures for the palladium ions' recovery has led to the development of a new series of macromolecules. Thus, this study presents a comparative behavior of two crown benzene ethers that modify the magnesium silicate surface used as adsorbent for palladium. These crown ethers are dibenzo18-crown-6 (DB18C6) and dibenzo 30-crown-10 (DB30C10). The obtained materials were characterized by scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDX) and Fourier-transform infrared spectroscopy (FT-IR). The specific surface area (BET) and point of zero charge (PZC) of the two materials were determined. The palladium ions' recovery from synthetic aqueous solutions studies aimed to establish the adsorption mechanism. For this desideratum, the kinetic, equilibrium and thermodynamic studies show that MgSiO3-DB30C10 have a higher adsorption capacity (35.68 mg g-1) compared to MgSiO3-DB18C6 (21.65 mg g-1). Thermodynamic studies highlight that the adsorption of Pd(II) on the two studied materials are spontaneous and endothermic processes. The positive values of the entropy (ΔS0) suggest that the studied adsorption processes show a higher disorder at the liquid/solid interface. Desorption studies were also performed, and it was found that the degree of desorption was 98.3%.

Preparation, optimization, and characterization of chitosan-sepiolite nanocomposite films for wound healing.

In this study, a series of chitosan-sepiolite (CS-SEP) nanocomposites films were prepared by using a conventional solution casting method. The effect of sepiolite on physicochemical and biological properties of the prepared nanocomposite films was studied by various techniques such as Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and x-ray diffraction (XRD) to name a few. In WCA measurements, the decrease of contact angle from 78.51° (CS) to 71.29° (CS7SEP3) reaffirms the water holding nature of sepiolite, which enables to create moist environment essentially required for wound healing. Further, addition of sepiolite tremendously increased WVTR, folding endurance, porosity, and blood clotting ability of the prepared nanocomposites. Furthermore, CS-SEP nanocomposite films exhibit better antibacterial activity than that of chitosan against gram positive (B. subtilis) and gram negative bacteria (E. coli). Moreover, the percentage of hemolysis and degradation study indicated that the prepared nanocomposite films were non-hemolytic in nature and decomposed nearly 40% in four weeks. In addition, cytotoxicity assay showed that the prepared nanocomposite film i.e. CS7SEP3 exhibited better cell viability and cell proliferation rate against L929 mouse fibroblast cells as compared to CS and hence, the prepared nanocomposite film can be used as a promising candidate for wound management.

Development and characterization of PVA-starch incorporated with coconut shell extract and sepiolite clay as an antioxidant film for active food packaging applications.

An active antioxidant film was fabricated by using polyvinyl alcohol (PVA) and corn starch (ST) and incorporated with and 3, 5, 10, and 20% (v/v) coconut shell extract (CSE) and sepiolite clay (SP) for the first time. The microstructure and physical properties of prepared films were characterized and examined. The addition of sepiolite clay to PVA improved the elongation break 15.57 to 69.24%, and water vapor permeability increased with the addition of CSE. In addition to CSE to films, the antioxidant activity properties of the films were enhanced up to 80%. Further, increasing the amount of CSE slightly affected the color of the active films. The thermal properties of films were enhanced with the addition of CSE and SP. The dispersion of SP in the PVA matrix was affected by an increase in CSE concentration in the PVA matrix. Remarkably, PVA-ST film-based sachets successfully improved the oxidative stability of packaged soybean oil. Our results suggest PVA-ST film containing CSE and sepiolite clay can be utilized as a novel antioxidant packaging material in the food processing industry.

A chitosan-based composite for adsorption of uranyl ions; mechanism, isothems, kinetics and thermodynamics.

The present paper describes a green and cost-effective approach to investigate chitosan-sepiolite (Ch-Sep) composite as an adsorbent for removal of UO22+ ions in aqueous solution. The Ch-Sep composite was prepared as a beads using with two cross-linking agents: tripolyphosphate (TPP) and epichlorohydrin (ECH). Their adsorption properties for the removal of UO22+ ions in aqueous solution by batch experimental conditions were studied. The adsorptive removal processes of UO22+ ions from aqueous solution were evaluated by Langmuir, Freundlich and Dubinin-Radushkevich isotherm models, and was found to be perfectly fit to the Langmuir model (R2 = 0.971). The maximum adsorption capacity was 0.220 mol kg-1 at 25 °C from Langmuir isotherm model. Adsorption energy was 12.1 kJ mol-1 indicating that the adsorption process was chemical. The adsorption kinetics followed the pseudo second order and intra particle diffusion models. The thermodynamics parameters of UO22+ ions removal from aqueous solution was confirmed spontaneous, endothermic and possible at higher temperatures behavior of adsorption process. The adsorption mechanism of UO22+ ions onto Ch-Sep composite beads was investigated by FT-IR and SEM analysis. These findings revealed the effectiveness and potential of the newly synthesized Ch-Sep composite beads for the removal of UO22+ ions.

Mg,Si-Co-Substituted Hydroxyapatite/Alginate Composite Beads Loaded with Raloxifene for Potential Use in Bone Tissue Regeneration.

Osteoporosis is a worldwide chronic disease characterized by increasing bone fragility and fracture likelihood. In the treatment of bone defects, materials based on calcium phosphates (CaPs) are used due to their high resemblance to bone mineral, their non-toxicity, and their affinity to ionic modifications and increasing osteogenic properties. Moreover, CaPs, especially hydroxyapatite (HA), can be successfully used as a vehicle for local drug delivery. Therefore, the aim of this work was to fabricate hydroxyapatite-based composite beads for potential use as local carriers for raloxifene. HA powder, modified with magnesium and silicon ions (Mg,Si-HA) (both of which play beneficial roles in bone formation), was used to prepare composite beads. As an organic matrix, sodium alginate with chondroitin sulphate and/or keratin was applied. Cross-linking of beads containing raloxifene hydrochloride (RAL) was carried out with Mg ions in order to additionally increase the concentration of this element on the material surface. The morphology and porosity of three different types of beads obtained in this work were characterized by scanning electron microscopy (SEM) and mercury intrusion porosimetry, respectively. The Mg and Si released from the Mg,Si-HA powder and from the beads were measured by inductively coupled plasma optical emission spectrometry (ICP-OES). In vitro RAL release profiles were investigated for 12 weeks and studied using UV/Vis spectroscopy. The beads were also subjected to in vitro biological tests on osteoblast and osteosarcoma cell lines. All the obtained beads revealed a spherical shape with a rough, porous surface. The beads based on chondroitin sulphate and keratin (CS/KER-RAL) with the lowest porosity resulted in the highest resistance to crushing. Results revealed that these beads possessed the most sustained drug release and no burst release effect. Based on the results, it was possible to select the optimal bead composition, consisting of a mixture of chondroitin sulphate and keratin.

Physicochemical characterization, drug release, and biocompatibility evaluation of carboxymethyl cellulose-based hydrogels reinforced with sepiolite nanoclay.

Polymer-clay nanocomposite hydrogel films (PCNCHFs) were prepared from caboxymethyl cellulose, polyvinylpyrrolidone, agar and nanosepiolite clay (0, 0.3, 0.5, 0.7, 0.9 and 1.5% reinforcement) by treating thermally in a simple, rapid, and inexpensive route. The PCNCHFs and its 5-fluorouracil (FU)-loaded composites (PCNCHFs@FU) were tested for FU release and characterized by FTIR, XRD, FE-SEM, EDX, DSC, and TGA analyses to investigate their structural, morphological, and thermal properties. The nanosepiolite-loaded polymer composites (PCNCHF1 to PCNCHF5) exhibited higher tensile strength than the pristine polymer hydrogel (PCNCHF0); consequently, the thermal properties (glass- and melting-transition) were improved. The PCNCHFs@FU demonstrated prolonged FU release at pH 7.4 for 32 h. The biocompatibility of PCNCHFs was tested against human skin fibroblast (CCDK) cells. The viability of cells exposed to all PCNCHFs was >95% after 72 h of culture. The live/dead assay show the proliferation of fibroblast cells, confirming the biocompatibility of the hydrogels. The pH-sensitive PCNCHFs@FU release could be suitable for drug release in cancer therapy, and the developed PCNCHFs may also be useful for tissue engineering, food packaging, and other biological applications.

Treatment of environmental contamination using sepiolite: current approaches and future potential.

To evaluate the potential of sepiolite-based materials to resolve environmental pollution problems, a study is needed which looks at the whole life cycle of material application, including the residual value of material classified as waste from the exploitation of sepiolite deposits in the region or from its processing and purification. This would also maximize value from the exploitation process and provide new potential for local waste management. We review the geographical distribution of sepiolite, its application in the treatment of potentially toxic elements in soil and across the wider landscape, an assessment of modification and compositional variation of sepiolite-based applications within site remediation and wastewater treatment. The potential of sepiolite-based technologies is widespread and a number of processes utilize sepiolite-derived materials. Along with its intrinsic characteristics, both the long-term durability and the cost-effectiveness of the application need to be considered, making it possible to design ready-to-use products with good market acceptance. From a critical analysis of the literature, the most frequently associated terms associated with sepiolite powder are the use of lime and bentonite, while fly ash ranked in the top ten of the most frequently used material with sepiolite. These add improved performance for the inclusion as a soil or wastewater treatment options, alone or applied in combination with other treatment methods. This approach needs an integrated assessment to establish economic viability and environmental performance. Applications are not commonly evaluated from a cost-benefit perspective, in particular in relation to case studies within geographical regions hosting primary sepiolite deposits and wastes that have the potential for beneficial reuse.

Alginate bionanocomposite films containing sepiolite modified with polyphenols from myrtle berries extract.

Alginate nanocomposite films incorporating sepiolite (Sep) modified with myrtle berries extract (MBE) rich in polyphenols were prepared by solution casting method. The effects of different extract concentrations on the film properties were determined by measuring physicochemical, mechanical and antioxidant properties of the films. Fourier transform infrared (FTIR) spectra indicated that strong interactions between the polyphenols present in the MBE and sepiolite were involved in the films. The results suggested that incorporation of Sep-MBE hybrids into the films improved elongation at break, tensile strength, water vapor and UV barrier properties compared to the control film. The antioxidant activity of the films was significantly improved and raised with increasing content of MBE. The release kinetics results of MBE polyphenols from the active films into alcoholic food simulant indicated that the addition of Sep-MBE hybrids to alginate film is able to slow the release of MBE polyphenols. This study revealed the benefits of incorporation of Sep-MBE hybrids into the alginate films and their potential application as active packaging films or coating material.

Preparation of organic-inorganic chitosan@silver/sepiolite composites with high synergistic antibacterial activity and stability.

Organic-inorganic antibacterial materials chitosan@silver/sepiolite (CTs@Ag/Sep) was prepared by grafting organometallic chelate of chitosan and silver on sepiolite. The prepared samples were characterized, and their antibacterial properties were detected. The carrier sepiolite was beneficial for the thermal stability of the composite material. The utilization of silver was enhanced and its amount of usage could be obviously reduced by introduction of nontoxic chitosan which was benefical for the formation of highly dispersed silver nanoparticles on the CTs@Ag/Sep by the interaction between the silver ion and the plentiful amino and hydroxyl groups on the chitosan, thus improved the antibacterial activities and stability. The average width of the inhibition zone of CTs@Ag/Sep against Staphylococcus aureus (S. aureus), Escherichia coli (E. coli) and Aspergillus niger were 51.8, 31.8, and 44.7 mm, respectively. The cytotoxicity of CTs@Ag/Sep was further evaluated with A549 cells, and the results indicated that it exhibited low cytotoxicity to eukaryotic cells.

Make proper surfaces for immobilization of enzymes: Immobilization of lipase and α-amylase on modified Na-sepiolite.

This paper has focused on making suitable carriers for the immobilization of α-amylase from Bacillus subtilis and lipase from Candida rugosa via adsorption on modified Na-sepiolite (SEP). Two modified carriers were prepared by changing the nature of SEP with cetrimonium bromide surfactant at concentrations below the CMC of the surfactant, to produce SEP with monolayer surfactant (MSEP) with hydrophobic properties and above the CMC of the surfactant to produce SEP with bilayer surfactant (BSEP) with hydrophilic properties. The enzymatic activity of immobilized lipase on MSEP (MSEPL) and immobilized α-amylase on BSEP (BSEPA) was successfully tested in the hydrolysis of olive oil and starch. The support modification and immobilization process were characterized by BET, XRD, and SEM techniques. The results demonstrated that the specific activity of MSEPL and BSEPA was 1.74 and 2.28 U/mg, respectively. The remained activity of MSEPL (56.7%) and BSEPA (40.4%) after their incubation at 60 °C for 4 h was much higher than that of free enzymes. The residual activity of MSEPL and BSEPA was 77.4% and 66.7%, after 30 days of storage at 4 °C. The MSEPL and BSEPA also showed good reusability, and their relative activities were 54.0% and 44.2% after ten cycles.

Analysis of particles from hamster lungs following pulmonary talc exposures: implications for pathogenicity.

BACKGROUND: Talc, a hydrous magnesium silicate, often used for genital hygiene purposes, is associated with ovarian carcinoma in case-control studies. Its potential to cause inflammation, injury, and functional changes in cells has been described. A complication of such studies is that talc preparations may be contaminated with other materials. A previous study by (Beck et al. Toxicol Appl Pharmacol 87:222-34, 1987) used a hamster model to study talc and granite dust exposure effects on various biochemical and cellular inflammatory markers. Our current study accessed key materials used in that 1987 study; we re-analyzed the original talc dust with contemporary scanning electron microscopy and energy dispersive x-ray analysis (SEM/EDX) for contaminants. We also examined the original bronchoalveolar lavage (BAL) cells with polarized light microscopy to quantify cell-associated birefringent particles to gain insight into the talc used. RESULTS: SEM/EDX analyses showed that asbestos fibers, quartz, and toxic metal particulates were below the limits of detection in the original talc powder. However, fibers with aspect ratios ≥3:1 accounted for 22% of instilled material, mostly as fibrous talc. Talc (based on Mg/Si atomic weight % ratio) was the most abundant chemical signature, and magnesium silicates with various other elements made up the remainder. BAL cell counts confirmed the presence of acute inflammation, which followed intratracheal instillation. Measurements of cell associated birefringent particles phagocytosis revealed significant differences among talc, granite, and control exposures with high initial uptake of talc compared to granite, but over the 14-day experiment, talc phagocytosis by lavaged cells was significantly less than that of granite. Phagocytosis of talc fibers by macrophages was observed, and birefringent particles were found in macrophages, neutrophils, and multinucleate giant cells in lavaged cells from talc-exposed animals. CONCLUSION: Our data support the contention that talc, even without asbestos and other known toxic contaminants, may elicit inflammation and contribute to lung disease. Our findings support the conclusions of (Beck et al. Toxicol Appl Pharmacol 87:222-34, 1987) study. By analyzing particulate exposures with polarized light microscopy and SEM/EDX, fibrous talc was identified and a distinctive pattern of impaired particulate ingestion was demonstrated.

Macro-Microporous Surface with Sulfonic Acid Groups and Micro-Nano Structures of PEEK/Nano Magnesium Silicate Composite Exhibiting Antibacterial Activity and Inducing Cell Responses.

PURPOSE: To improve the surface bio-properties of polyetheretherketone (PEEK)/nano magnesium silicate (n-MS) composite (PC). MATERIALS AND METHODS: The surface of PC was firstly treated by particle impact (PCP) and subsequently modified by concentrated sulfuric acid (PCPS). RESULTS: PCPS surface exhibited not only macropores with sizes of about 150 µm (fabricated by particle impact) but also micropores with sizes of about 2 µm (created by sulfonation of PEEK) on the macroporous walls, and sulfonic acid (-SO3H) groups were introduced on PCPS surface. In addition, many n-MS nanoparticles were exposed on the microporous walls, which formed micro-nano structures. Moreover, the surface roughness and hydrophilicity of PCPS were obviously enhanced as compared with PC and PCP. Moreover, the apatite mineralization of PCPS in simulated body fluid (SBF) was obviously improved as compared with PC. Furthermore, compared with PC and PCP, PCPS exhibited antibacterial performances due to the presence of -SO3H groups. In addition, the responses (eg, adhesion and proliferation as well as differentiation) of bone marrow mesenchymal stem cell of rat to PCPS were significantly promoted as compared with PC and PCP. CONCLUSION: PCPS with macro-microporous surface containing -SO3H groups and micro-nano structures exhibited antibacterial activity and induced cell responses, which might possess large potential for bone substitute and repair.

1,3,5-Triethynylbenzene and melamine as monomers to synthesize three-dimensional network porous aromatic frameworks based silica/florisil for determination of carbendazim and thiabendazole in spinach.

In this study, the new and efficient three-dimensional network porous aromatic frameworks materials called Silica-PAFs-a, Florisil-PAFs-a, Silica-PAFs-b, and Florisil-PAFs-b were first synthesized. The properties of materials were analyzed by five characterization methods. The materials were used as adsorbents in pipette-tip solid-phase extraction for the effective determination of carbendazim and thiabendazole in spinach sample. Meanwhile, the obtained materials were tested by static adsorption and dynamic adsorption. The result showed that the specific surface area of materials greatly increased after introducing three-dimensional network porous aromatic frameworks. Microstructural modification exposed a large number of amino reactive groups that made them have a better adsorption amount for the two targets. The calibration graphs of carbendazim and thiabendazole in methanol were linear over 0.10-300.0 µg/mL, and the limits of detection and quantification were 0.00546 and 0.0182 µg/mL, and 0.00741 and 0.0247µg/mL respectively. A reliable analytical method was developed for recognition targets in spinach sample by Silica-PAFs-b with satisfactory extraction recoveries (96.25 and 100.51%). The proposed method using the material was applied for trace analysis of the carbendazim and thiabendazole residue.

The Immobilization Effect of Natural Mineral Materials on Cr(VI) Remediation in Water and Soil.

The effects of sepiolite, montmorillonite, and attapulgite on the removal and immobilization of Cr(VI) in water and soil were studied. X-ray diffraction (XRD) characterizations showed that the purities of these three mineral materials decreased in the following order: montmorillonite > attapulgite > sepiolite, and that their surface molecular bond types were similar. The adsorption potential of Cr(VI) in aqueous solutions of the three mineral materials was in the following order: sepiolite > attapulgite > montmorillonite. The adsorption mechanism for attapulgite was consistent with the Freundlich isotherm adsorption model, whereas that for montmorillonite was more consistent with the Langmuir model. Sepiolite had a good fitting effect for both isothermal adsorption models. For montmorillonite and attapulgite, a lower pH corresponded to a higher removal of Cr(VI). For sepiolite, however, the removal efficiency of Cr(VI) from an aqueous solution was the lowest at a pH of approximately 5.0. The results of the soil toxicity characteristic leaching procedure showed that, following the addition of 15% sepiolite, attapulgite, or montmorillonite to the contaminated soil, Cr(VI) concentrations in the leachates decreased by 16.8%, 18.9%, and 15.9%, respectively, and the total Cr concentrations in the leachates were reduced by 21.2%, 29.2%, and 17.6%. Of the three mineral materials, attapulgite demonstrated the highest Cr(VI) immobilization efficiency in soil. This study emphasizes the effect of attapulgite on the immobilization of Cr(VI) in soil and aqueous solutions, thus providing a theoretical basis for the potential application of natural mineral material remediation of Cr(VI)-contaminated aqueous solutions and soils.

Clay Composites for Thermal Energy Storage: A Review.

The development of novel materials and approaches for effective energy consumption and the employment of renewable energy sources is one of the current trends in modern material science. With this respect, the number of researches is focused on the effective harvesting and storage of solar energy for various applications. Phase change materials (PCMs) are known to be able to store thermal energy of the sunlight due to adsorption and release of latent heat through reversible phase transitions. Therefore, PCMs are promising as functional additives to construction materials and paints for advanced thermoregulation in building and industry. However, bare PCMs have limited practical applications. Organic PCMs like paraffins suffer from material leakage when undergoing in a liquid state while inorganic ones like salt hydrates lack long-term stability after multiple phase transitions. To avoid this, the loading of PCMs in porous matrices are intensively studied along with the thermal properties of the resulted composites. The loading of PCMs in microcontainers of natural porous or layered clay materials appears as a simple and cost-effective method of encapsulation significantly improving the shape and cyclic stability of PCMs. Additionally, the inclusion of functional clay containers into construction materials allows for improving their mechanical and flame-retardant properties. This article summarizes the recent progress in the preparation of composites based on PCM-loaded clay microcontainers along with their future perspectives as functional additives in thermo-regulating materials.

Hierarchical porous Mg2SiO4-CoFe2O4 nanomagnetic scaffold for bone cancer therapy and regeneration: Surface modification and in vitro studies.

3D multifunctional bone scaffolds have recently attracted more attention in bone tissue engineering because of addressing critical issues like bone cancer and inflammation beside bone regeneration. In this study, a 3D bone scaffold is fabricated from Mg2SiO4-CoFe2O4 nanocomposite which is synthesized via a two-step synthesis strategy and then the scaffold's surface is modified with poly-3-hydroxybutyrate (P3HB)-ordered mesoporous magnesium silicate (OMMS) composite to improve its physicochemical and biological properties. The Mg2SiO4-CoFe2O4 scaffold is fabricated through polymer sponge technique and the scaffold exhibits an interconnected porous structure in the range of 100-600 µm. The scaffold is then coated with OMMS/P3HB composite via dip coating and the physical, chemical, and biological-related properties of OMMS/P3HB composite-coated scaffold are assessed and compared to the non-coated and P3HB-coated scaffolds in vitro. It is found that, on the one hand, P3HB increases the cell attachment, proliferation, and compressive strength of the scaffold, but on the other hand, it weakens the bioactivity kinetic. Addition of OMMS to the coating composition is accompanied with significant increase in bioactivity kinetic. Besides, OMMS/P3HB composite-coated scaffold exhibits higher drug loading capacity and more controlled release manner up to 240 h than the other samples because of OMMS which has a high surface area and ordered mesoporous structure suitable for controlled release applications. The overall results indicate that OMMS/P3HB coating on Mg2SiO4-CoFe2O4 scaffold leads to a great improvement in bioactivity, drug delivery potential, compressive strength, cell viability, and proliferation. Moreover, OMMS/P3HB composite-coated scaffold has heat generation capability for hyperthermia-based bone cancer therapy and so it is suggested as a multifunctional scaffold with great potentials for bone cancer therapy and regeneration.

Adsorption of Cd and Pb in contaminated gleysol by composite treatment of sepiolite, organic manure and lime in field and batch experiments.

Contamination of arable land with trace metals is a global environmental issue which has serious consequences on human health and food security. Present study evaluates the adsorption of cadmium (Cd) and lead (Pb) by using different quantities of composite of sepiolite, organic manure and lime (SOL) at field and laboratory scale (batch experiments). Characterization of SOL by SEM, EDS and FTIR spectroscopy revealed the presence of elemental and functional groups (hydroxyl, C⋯H and -COOH groups) on its surface. The field experiment was performed in a paddy field of gleysol having moderate contamination of Cd and Pb (0.64 mg kg-1 and 53.44 mg kg-1). Here, different rates of SOL (0.25, 0.5, 1, 1.5 and 2% w/w) were applied by growing low and high Cd accumulator rice cultivars. Application of SOL at 2% w/w showed considerable efficiency to increase soil pH (up to 19%) and to reduce available Cd (42-66%) and Pb (22-55%) as compared to the control. Moreover, its application reduced metal contents in roots, shoots and grains of rice by 31%, 36% and 72% (for Cd) and 41%, 81% and 84% (for Pb), respectively in low accumulator cultivar. Further, the batch sorption experiment was performed to evaluate the adsorption capacity of SOL in a wide range of contamination. Obtained sorption data was better fitted to the Langmuir equation. Our results highlight the strong efficiency of composite treatment for an enhanced in-situ metal immobilization under field and lab conditions. Further, applied treatments greatly reduced the metal contents in rice grains. In a nut shell, application of SOL in a contaminated gleysol should be considered for soil remediation and safe food production.

Effects of Cd-resistant bacteria and calcium carbonate + sepiolite on Cd availability in contaminated paddy soil and on Cd accumulation in brown rice grains.

A pot experiment was conducted to evaluate the effects of combined application of cadmium (Cd)-resistant bacteria (J) and calcium carbonate + sepiolite (G) on both Cd bioavailability in contaminated paddy soil and on Cd accumulation in rice plants. Adding the mixture (J + G) to the soils significantly increased soil pH, decreased extractable Cd contents, and increased Fe/Mn-oxide Cd and organic-bound Cd contents. The applying of J + G, J and G decreased Cd contents in various rice tissues (roots, stems and leaves, husks, and brown rice grains) to different degrees. Compared with those of the CK, Cd contents decreased by 17.8%-53.3% in the roots, 12.3%-27.4% in the stems and leaves, 25.4%-44.6% in the husks, and 28.8%-55.7% in the brown rice grains for the application of J + G; Cd contents decreased by 8.2%-28.5% in the roots, 11.5%-32.0% in the husks, and 27.8%-45.9% in the brown rice grains for the application of J; Cd contents decreased by 12.9%-26.5% in the roots, in the stems and leaves decreased by 4.6%-34.1% in the stems and leaves, 60.2%-79.7% in the husks, and 35.7%-47.6% in the brown rice grains for the application of G. The alone application of bacteria (J) could reduce the bioavailability of Cd in soil and the contents of Cd in brown rice grains to some extent. Moreover, when the bacteria were applied in combination with mineral (J + G), it was a more effective method than the alone application of J or G to reduce the soil Cd bioavailability. Under all the tested conditions, applications of J4+G4 (320 mL kg-1 of J + 8 g kg-1 of G) resulted in the greatest reduction in Cd contents in brown rice grains. Overall, the results indicated that the combination of Cd-resistant bacteria and mineral material could effectively reduce Cd bioavailability in paddy soils and inhibit Cd accumulation in brown rice grains.

Effects of Sepiolite and Biochar on Enzyme Activity of Soil Contaminated by Cd and Atrazine.

The effects of sepiolite and biochar on the enzymatic activities of the soil in Cd- and atrazine-contaminated soils were studied. During the growth of pakchoi, the activities of acid phosphatase, sucrase, acid protease, and cellulase decreased, catalase activity increased, and urease activity decreased first and then increased. At the first harvest, compared with that for the control group, the soil pH after treatment with remediation materials increased from 5.41 to 7.43; the activities of urease, acid protease, and catalase increased by 62.8%, 38.6%, and 86.1%, respectively. And the activities of sucrase and acid phosphatase decreased by 17.3% and 24.7%, respectively. At the second harvest, the activities of acid phosphatase, acid protease, and cellulase continued to increase, but those of sucrase and catalase decreased. The results showed that soil enzyme activity was closely related to the type and addition of remediation materials, as well as the type of the enzyme.