Insights into the Effect of Chitosan and ß-Cyclodextrin Hybridization of Zeolite-A on Its Physicochemical and Cytotoxic Properties as a Bio-Carrier for 5-Fluorouracil: Equilibrium and Release Kinetics Studies.

Synthetic zeolite-A (ZA) was hybridized with two different biopolymers (chitosan and ß-cyclodextrin) producing biocompatible chitosan/zeolite-A (CS/ZA) and ß-cyclodextrin/zeolite-A (CD/ZA) biocomposites. The synthetic composites were assessed as bio-carriers of the 5-fluorouracil drug (5-Fu) with enhanced properties, highlighting the impact of the polymer type. The hybridization by the two biopolymers resulted in notable increases in the 5-Fu loading capacities, to 218.2 mg/g (CS/ZA) and 291.3 mg/g (CD/ZA), as compared to ZA (134.2 mg/g). The loading behaviors using ZA as well as CS/ZA and CD/ZA were illustrated based on the classic kinetics properties of pseudo-first-order kinetics (R2 > 0.95) and the traditional Langmuir isotherm (R2 = 0.99). CD/ZA shows a significantly higher active site density (102.7 mg/g) in comparison to CS/ZA (64 mg/g) and ZA (35.8 mg/g). The number of loaded 5-Fu per site of ZA, CS/ZA, and CD/ZA (>1) validates the vertical ordering of the loaded drug ions by multi-molecular processes. These processes are mainly physical mechanisms based on the determined Gaussian energy (<8 kJ/mol) and loading energy (<40 kJ/mol). Both the CS/ZA and CD/ZA 5-Fu release activities display continuous and controlled profiles up to 80 h, with CD/ZA exhibiting much faster release. According to the release kinetics studies, the release processes contain non-Fickian transport release properties, suggesting cooperative diffusion and erosion release mechanisms. The cytotoxicity of 5-Fu is also significantly enhanced by these carriers: 5-Fu/ZA (11.72% cell viability), 5-Fu/CS/ZA (5.43% cell viability), and 5-Fu/CD/ZA (1.83% cell viability).

Synthesis and Characterization of Methoxy-Exfoliated Montmorillonite Nanosheets as Potential Carriers of 5-Fluorouracil Drug with Enhanced Loading, Release, and Cytotoxicity Properties.

Natural bentonite clay (BE) underwent modification steps that involved the exfoliation of its layers into separated nanosheets (EXBE) and further functionalization of these sheets with methanol, forming methoxy-exfoliated bentonite (Mth/EXBE). The synthetically modified products were investigated as enhanced carriers of 5-fluorouracil as compared to raw bentonite. The modification process strongly induced loading properties that increased to 214.4 mg/g (EXBE) and 282.6 mg/g (Mth/EXBE) instead of 124.9 mg/g for bentonite. The loading behaviors were illustrated based on the kinetic (pseudo-first-order model), classic isotherm (Langmuir model), and advanced isotherm modeling (monolayer model of one energy). The Mth/EBE carrier displays significantly higher loading site density (95.9 mg/g) as compared to EXBE (66.2 mg/g) and BE (44.9 mg/g). The loading numbers of 5-Fu in each site of BE, EXBE, and Mth/EXBE (>1) reflect the vertical orientation of these loaded ions involving multi-molecular processes. The loading processes that occurred appeared to be controlled by complex physical and weak chemical mechanisms, considering both Gaussian energy (<8 KJ/mol) as well as loading energy (<40 KJ/mol). The releasing patterns of EXBE and Mth/EXBE exhibit prolonged and continuous properties up to 100 h, with Mth/EXBE displaying much faster behaviors. Based on the release kinetic modeling, the release reactions exhibit non-Fickian transport release properties, validating cooperative diffusion and erosion release mechanisms. The cytotoxicity of 5-Fu is also significantly enhanced by these carriers: 5-Fu/BE (8.6% cell viability), 5-Fu/EXBE (2.21% cell viability), and 5-Fu/Mth/EXBE (0.73% cell viability).

Insight into the Morphological Properties of Nano-Kaolinite (Nanoscrolls and Nanosheets) on Its Qualification as Delivery Structure of Oxaliplatin: Loading, Release, and Kinetic Studies.

Natural kaolinite underwent advanced morphological-modification processes that involved exfoliation of its layers into separated single nanosheets (KNs) and scrolled nanoparticles as nanotubes (KNTs). Synthetic nanostructures have been characterized as advanced and effective oxaliplatin-medication (OXAP) delivery systems. The morphological-transformation processes resulted in a remarkable enhancement in the loading capacity to 304.9 mg/g (KNs) and 473 mg/g (KNTs) instead of 29.6 mg/g for raw kaolinite. The loading reactions that occurred by KNs and KNTs displayed classic pseudo-first-order kinetics (R2 > 0.90) and conventional Langmuir isotherms (R2 = 0.99). KNTs exhibit a higher active site density (80.8 mg/g) in comparison to KNs (66.3 mg/g) and raw kaolinite (6.5 mg/g). Furthermore, compared to KNs and raw kaolinite, each site on the surface of KNTs may hold up to six molecules of OXAP (n = 5.8), in comparison with five molecules for KNs. This was accomplished by multi-molecular processes, including physical mechanisms considering both the Gaussian energy (<8 KJ/mol) and the loading energy (<40 KJ/mol). The release activity of OXAP from KNs and KNTs exhibits continuous and regulated profiles up to 100 h, either by KNs or KNTs, with substantially faster characteristics for KNTs. Based on the release kinetic investigations, the release processes have non-Fickian transport-release features, indicating cooperative-diffusion and erosion-release mechanisms. The synthesized structures have a significant cytotoxicity impact on HCT-116 cancer cell lines (KNs (71.4% cell viability and 143.6 g/mL IC-50); KNTs (11.3% cell viability and 114.3 g/mL IC-50). Additionally, these carriers dramatically increase OXAP's cytotoxicity (2.04% cell viability, 15.4 g/mL IC-50 (OXAP/KNs); 0.6% cell viability, 4.5 g/mL IC-50 (OXAP/KNTs)).

Steric and Energetic Studies on the Synergetic Enhancement Effect of Integrated Polyaniline on the Adsorption Properties of Toxic Basic and Acidic Dyes by Polyaniline/Zeolite-A Composite.

The synergetic enhancement effect of the polyaniline (PANI) integration process on the adsorption properties of the PANI/zeolite-A composite (PANI/ZA) as an adsorbent for malachite green and Congo red synthetic dyes was evaluated based on classic equilibrium modelling in addition to the steric and energetic parameters of advanced isotherm studies. The PANI/ZA composite displays enhanced adsorption capacities for both methylene blue (270.9 mg/g) and Congo red (235.5 mg/g) as compared to ZA particles (methylene blue (179.6 mg/g) and Congo red (140.3 mg/g)). The reported enhancement was illustrated based on the steric parameters of active site density (Nm) and the number of adsorbed dyes per active site (n). The integration of PANI strongly induced the quantities of the existing active sites that have enhanced affinities towards both methylene blue (109.2 mg/g) and Congo red (92.9 mg/g) as compared to the present sites on the surface of ZA. Every site on the surface of PANI/ZA can adsorb about four methylene blue molecules and five Congo red molecules, signifying the vertical orientation of their adsorbed ions and their uptake by multi-molecular mechanisms. The energetic investigation of the methylene blue (-10.26 to -16.8 kJ/mol) and Congo red (-9.38 to -16.49 kJ/mol) adsorption reactions by PANI/ZA suggested the operation of physical mechanisms during their uptake by PANI/ZA. These mechanisms might involve van der Waals forces, dipole bonding forces, and hydrogen bonding (<30 kJ/mol). The evaluated thermodynamic functions, including enthalpy, internal energy, and entropy, validate the exothermic and spontaneous behaviours of the methylene blue and Congo red uptake processes by PANI/ZA.

Biological Activities of Sargassum Algae Mediated ZnO and Co Doped ZnO Nanoparticles as Enhanced Antioxidant and Anti-Diabetic Agents.

Brown macroalgae (BMG) were used as carriers for ZnO (ZnO/BMG) and cobalt-doped ZnO (Co-ZnO/BMG) via facile microwave-assisted hydrothermal synthesis. The multifunctional structures of synthesized composites were evaluated as enhanced antioxidant and anti-diabetic agents based on the synergistic effects of ZnO, Co-ZnO, and BMG. BMG substrate incorporation and cobalt doping notably enhanced the bioactivity of the synthesized ZnO nanoparticles. As an antioxidant, the Co-ZnO/BMG composite exhibited highly effective scavenging properties for the common free reactive oxygen radicals (DPPH [89.6 ± 1.5%], nitric oxide [90.2 ± 1.3%], ABTS [87.7 ± 1.8%], and O2●- [46.7 ± 1.9%]) as compared to ascorbic acid. Additionally, its anti-diabetic activity was enhanced significantly and strongly inhibited essential oxidative enzymes (porcine α-amylase (90.6 ± 1.5%), crude α-amylase (84.3 ± 1.8%), pancreatic α-glucosidase (95.7 ± 1.4%), crude intestinal α-glucosidase (93.4 ± 1.8%), and amyloglucosidase (96.2 ± 1.4%)). Co-ZnO/BMG inhibitory activity was higher than that of miglitol, and in some cases, higher than or close to that of acarbose. Therefore, the synthetic Co-ZnO/BMG composite can be used as a commercial anti-diabetic and antioxidant agent, considering the cost and adverse side effects of current drugs. The results also demonstrate the impact of cobalt doping and BMG integration on the biological activity of ZnO.

Investigating the impacts of heavy metal(loid)s on ecology and human health in the lower basin of Hungary's Danube River: A Python and Monte Carlo simulation-based study.

This study aimed to determine the environmental and health risks of the heavy metal levels in the Danube River in Hungary. The metals, including Fe, Mn, Zn, Cu, Ni, Cr, Pb, and As, were measured in the period from 2013 to 2019. The Spearman correlation and heatmap cluster analysis were utilized to determine the origin of pollution and the factors that control surface water quality. Several indices, such as the heavy metal pollution index (HPI), metal index (MI), hazard quotient oral and dermal (HQ), hazard index oral and dermal (HI), and carcinogenic risk (CR), were conducted to evaluate the potential risks for the environment and human health. The values of the HPI were between the range of 15 < HPI < 30, which indicated moderate pollution; however, the MI results showed high pollution in Dunaföldvár and Hercegszántó cities. The ecological risk (RI < 30) and HI values (< 1) showed low environmental risks and non-carcinogenic impacts of the existing metals, either on adults or children. The mean CR value of oral arsenic was 2.2E-04 and 2.5E-04 during April-September and October-March, respectively, indicating that children were the most vulnerable to arsenic-carcinogenic oral effects. While lead's CR oral values for children during April-September exceeded the threshold of 1.0E-04, chromium's oral and dermal CR values for both adults and children were 2.08E-04, 6.11E-04, 1.97E-04, and 5.82E-04 during April-September and October-March, respectively. These results demonstrate the potential carcinogenic risks related to chromium exposure within the two pathways in Hungary and highlight the need for effective measures to mitigate these risks.

Insights into the green doping of clinoptilolite with Na+ ions (Na+/Clino) as a nanocatalyst in the conversion of palm oil into biodiesel; optimization and mechanism.

The critical demand for eco-friendly, renewable, and safe energy resources is an essential issue encountered in the contemporary world. The catalytic transesterification of plant oils into biodiesel was assessed as promising a technique for providing new forms of clean and safe fuel. Natural clinoptilolite was doped with Na+ ions by green chemical reactions between sodium nitrite and green tea extract, producing a novel modified structure (Na+/Clino). The Na+/Clino product had an enhanced total basicity (6.41 mmol OH/g), ion exchange capacity (387 meq/100 g), and surface area (312.7 m2 g-1), which qualified it to be used as a potential basic catalyst for the transesterification of palm oil. Transesterification tests were statistically assessed using a response surface methodology and a central composite design. Considering the effect of how the significant factors interact with each other, the synthetic Na+/Clino achieved a 96.4% experimental biodiesel yield after 70 min at 100 °C in the presence of 2.75 wt% catalyst loading and a 12.5:1 methanol-to-palm-oil ratio. Based on the optimization function of the statistical model, the performance of Na+/Clino can theoretically be enhanced to increase the yield to 98.2% by expanding the test time to 85 min and the loading value to 3 wt%. The product yielded by the Na+/ClinO process is of adequate technical properties, considering the international levels for standard biodiesel (EN 14214 and ASTM D-6751). Finally, the prepared green Na+ doped clinoptilolite had excellent recyclability as a heterogeneous basic catalyst and displayed higher efficiency than several species of previously studied heterogeneous and homogenous catalysts.

Insight into the role of the zeolitization process in enhancing the adsorption performance of kaolinite/diatomite geopolymer for effective retention of Sr (II) ions; batch and column studies.

Diatomite/kaolinite-based geopolymer (GP) was synthesized and incorporated in zeolitization process (Z/GP) to investigate the role of the zeolite phases in inducing its retention capacity of the dissolved Sr (II) ions in water. The retention of Sr (II) ions using Z/GP in comparison with GP was evaluated based on both batch and fixed-bed column studies. In the batch study, the zeolitized geopolymer (Z/GP) shows enhancement in the Sr (II) retention capacity (193.7 mg/g) as compared to the normal geopolymer (102 mg/g). Moreover, the recyclability studies demonstrate higher stability for Z/GP than GP with a retention percentage higher than 90% for five reusing runs. The kinetic and the equilibrium properties of the occurred Sr (II) retention reactions follow the assumption of the Pseudo-Second order model (R2 > 0.96) and Langmuir model (R2 > 0.97), respectively. The Gaussian energies (15.4 kJ/mol (GP) and 11.47 kJ/mol (Z/GP)) related to retention mechanism of chemical type and within the suggested range for the zeolitic ion exchange processes. The Sr (II) retention reactions by GP and Z/GP are of spontaneous and exothermic properties which qualifies the products to be used at low-temperature conditions (20 °C). The column studies also declared higher performance for the Z/GP fixed bed as compared to the normal GP bed considering the total Sr (II) retention percentage (72.9%), treated volume (8 L), saturation time (1620 min), and a maximum capacity of Z/GP particles in the bed (567.6 mg/g).

Synthesis of zeolite/geopolymer composite for enhanced sequestration of phosphate (PO43-) and ammonium (NH4+) ions; equilibrium properties and realistic study.

Zeolite impeded geopolymer (Z/G) was synthesized from natural kaolinite and diatomite. The structure (Z/G) was characterized as an enhanced adsorbent for PO43- and NH4+ ions from aqueous solutions, groundwater, and sewage water. The synthetic Z/G structure exhibits sequestration capacities of 206 mg/g and 140 mg/g for PO43- and NH4+, respectively which are higher values than the recognized results for the geopolymer and other adsorbents in literature. The sequestration reactions of PO43- and NH4+ by Z/G are of Pseudo-Second order kinetic behavior considering both the Chi-squared (χ2) and correlation coefficient (R2) values. The sequestration reactions occur in homogenous and monolayer forms considering their agreement with Langmuir behavior. The Gaussian energies (12.4 kJ/mol (PO43-) and 10.47 kJ/mol (NH4+)) demonstrate the operation of a chemical sequestration mechanism that might be involved zeolitic ion exchange process and chemical complexation. Additionally, these reactions are exothermic processes of spontaneous and favorable properties based on thermodynamic studies. The Z/G structure is of significant affinity for both PO43- and NH4+ even in the existence of other anions as Cl-, HCO3-, SO42-, and NO3-. Finally, the structure used effectively in the purification of groundwater and sewage water from PO43- and NH4+ in addition to nitrate, sulfate, and some metal ions.

Instantaneous oxidation of levofloxacin as toxic pharmaceutical residuals in water using clay nanotubes decorated by ZnO (ZnO/KNTs) as a novel photocatalyst under visible light source.

Kaolinite nanotubes were synthesized by a simple scrolling process and decorated by ZnO nanoparticles as a novel nanocomposite (ZnO/KNTs). The synthetic ZnO/KNTs composite was characterized as an effective photocatalyst in the oxidation of levofloxacin pharmaceutical residuals in the water resources. The composite displays a surface area of 95.4 m2/g, average pore diameter of 5.8 nm, and bandgap energy of 2.12 eV. It is of high catalytic activity in the oxidation of levofloxacin in the presence of visible light source. The complete oxidation for 10 mg/L of levofloxacin was recognized after 55 min, 45 min, and 30 min with applying 30 mg, 40 mg, and 50 mg of ZnO/KNTs as catalyst dosage, respectively. Additionally, it achieved complete oxidation for 20 mg/L and 30 mg/L of levofloxacin after 45 min and 75 min, respectively using 50 mg as catalyst dosage. The degradation efficiency was confirmed by detecting the residual TOC after the treatment tests and the formed intermediate compounds were identified to suggest the degradation pathways. In addition to the oxidation pathway, the mechanism was evaluated based on the active trapping tests that proved the dominance of hydroxyl radicals as the essential active species. Finally, the ZnO/KNTs composite is of promising recyclability properties and achieved better results than several studied photocatalysts in literature.

Insight into the photocatalytic properties of diatomite@Ni/NiO composite for effective photo-degradation of malachite green dye and photo-reduction of Cr (VI) under visible light.

Diatomite frustules decorated by nano Ni/NiO nanoparticles (Diatomite@Ni/NiO) were synthesized as a novel photocatalyst for effective degradation of malachite green cationic dye (M.G) and photocatalytic-reduction of Cr (VI) ions. The composite was characterized by different analytical techniques and revealed enhancing in the surface area (400 m2/g), 5.8 nm as average pore diameter and showed lower band gap energy (1.71 eV) than NiO as single phase. The photocatalytic activity of the composite in the removal of M.G and reduction of Cr (VI) was evaluated under visible light considering the pH, illumination time, catalyst mass, and the pollutants concentrations. The results revealed complete removal of 25 mg/L M.G can be achieved using 20 mg, 30 mg, 40 mg and 50 mg of the after 150 min, 90 min, 60 min, and 30 min, respectively. The complete degradation of 50 mg/L can be obtained after 240 min, 90 min, and 60 min using 20 mg, 40 mg, and 50 mg of the catalyst, respectively. This also was reported for the photocatlytic-reduction of 25 mg/L of Cr(VI) ions as the complete reduction was estimated after 180 min, 60 min and 30 min using 20 mg, 40 mg, and 50 mg, respectively. Also, 50 mg/L of Cr (VI) can be completely reduced after 240 min, 90 min, and 60 min using 20 mg, 40 mg, and 50 mg as catalyst dosage, respectively. The photocatalytic degradation of M.G controlled mainly by the generated electron-hole pairs and the superoxide species while the photocatalytic-reduction of Cr (VI) controlled mainly by the directly excited electrons of Ni/NiO and partially by the formed superoxide radicals. Hence, the synthetic diatomite@Ni/NiO composite can be considered as potential photocatalyst in the degradation of M.G dye and photoreduction of Cr (VI) ions.

Promoting the decontamination of different types of water pollutants (Cd2+, safranin dye, and phosphate) using a novel structure of exfoliated bentonite admixed with cellulose nanofiber.

Exfoliated bentonite sheets admixed with nano-cellulose fibers (EXB/CF) were prepared as advanced bio-composite of enhanced decontamination properties for different species of water pollutants (Cd2+, safranin dye, and phosphate). The composite achieved promising adsorption capacities with experimental values of 206.8 mg/g (Cd2+), 336 mg/g (safranin), and 296 mg/g (phosphate); and predicted maximum capacities of 212.9 mg/g (Cd2+), 341 mg/g (safranin), and 305 mg/g (phosphate). The adsorption systems for the three species follow the Freundlich isotherm model and Pseudo-First order as kinetic model considering both the linear and nonlinear fitting demonstrating heterogeneous and multilayer uptake properties of physisorption type. The operation of physisorption mechanisms was supported by the obtained adsorption energies from D-R model that are less than 8 kJ/mol as well as the calculated free energies and enthalpies. The thermodynamic investigation revealed the nature of the adsorption reactions of the three pollutants by EXB/CF as exothermic, favorable, and spontaneous reactions. The EXB/CF composite also is of significant recyclability value and applied in five decontamination reusing runs for Cd2+, safranin dye, and phosphate achieving promising removal percentages.

Photocatalytic degradation of malachite green dye using chitosan supported ZnO and Ce-ZnO nano-flowers under visible light.

Two types of chitosan-based composites (chitosan/ZnO and chitosan/Ce-ZnO composites) were synthesized under microwave irradiation and characterized as advanced catalysts of enhanced photocatalytic activity under the visible light. The morphological investigation reflected the formation of ZnO and Ce doped ZnO at stunning micro flowers of nano limps. Additionally, the optical studies reflected a reduction in the bandgap of ZnO from 3.3 eV to 2.85 eV and 2.5 eV after supporting it onto chitosan chains and after doping it with cerium, respectively. The synthetic composites were applied in photocatalytic removal of malachite green dye under a visible light source. The synthetic CH/ZnO and CH/Ce-ZnO showed enhancement in the photocatalytic removal of M.G by 54% and 87%, respectively, as compared to the pure ZnO. The synthetic composites are of high stability and can be reused for five photocatalytic degradation cycles at stunning removal percentages. The main oxidizing radicals during the removal of M.G by CH/ZnO are the generated electron-hole pairs as well as the hydroxyl radicals. The effective species in CH/Ce-ZnO photocatalytic system are the photogenerated hydroxyl radicals followed by the electron-hole pairs.

Enhanced photocatalytic removal of Safranin-T dye under sunlight within minute time intervals using heulandite/polyaniline@ nickel oxide composite as a novel photocatalyst.

Natural zeolite heulandite/polyaniline composite (Hu/PANI) was synthesized for the first time as catalyst support for nickel oxide photocatalyst (Hu/PANI@Ni2O3). The structural, chemical, morphological, textural and optical properties were investigated using different techniques. The synthetic Ni2O3 crystals showed well developed flaky habits with diameter range 200-400 nm and length range 1-4 µm. The estimated band gap energies of Hu/PANI composite and Hu/PANI@Ni2O3 composite are 1.8 eV and 1.46 eV, respectively, which are remarkably smaller than the recorded value for pure nickel oxide. The photocatalytic properties of Hu/PANI@Ni2O3 composite for efficient degradation of safranin-T dye were evaluated under sunlight as a function of irradiation time, initial dye concentration, catalyst mass, solution pH, and the catalyst stability. Hu/PANI@Ni2O3 composite exhibits amazing photocatalytic degradation efficiency for safranin dye, whereas 80%, 98%, and ~ 100% of 5 mg/l dye were removed after only 1 min of solar irradiation using 0.025, 0.03, and 0.035 g of Hu/PANI@Ni2O3, respectively. The higher concentrations of the dye (10-50 mg/L) can be fully removed within minutes by increasing the solution pH or using higher doses from the Hu/PANI@Ni2O3 catalyst. The removal percentage achieved the maximum value at the alkaline conditions. Also, the Hu/PANI@Ni2O3 displayed high stability and remain 84.5% of the initial photocatalytic efficiency after 5 runs. Additionally, the composite can be used effectively in the removal of different types of dyes and mixed dyes within the same time intervals. Thus, loading of nickel oxide onto hybrid Hu/PANI composite as a catalyst support achieved amazing photocatalytic degradation capacity.

Superior removal of Co2+, Cu2+ and Zn2+ contaminants from water utilizing spongy Ni/Fe carbonate-fluorapatite; preparation, application and mechanism.

Spongy Ni/Fe carbonate - fluorapatite was synthesized from natural phosphorite enriched with iron impurities. The morphological, chemical and structural features of the product were estimated using several techniques as XRD, SEM, EDX, and FT-IR. It exhibits spongy structure of nano and micro-pores. The average crystallite size is about 8.27 nm. The suitability of the product for considerable decontamination of Zn2+, Co2+, and Cu2+, ions from water was studied based on several reacting parameters. The equilibrium was attained after 240 min for Zn2+ and Co2+ ions while the adsorption equilibrium of Cu2+ reached after 120 min. The adsorption data for the selected metals was represented well by a pseudo-second-order model which revealed chemisorption uptake. The equilibrium studies were appraised based on traditional models and two advanced models were designed according to the statistical physical theories. The adsorption results highly fitted with Langmuir model followed rather than the other models. This indicated a monolayer adsorption for the metal ions by spongy Ni/Fe carbonate - fluorapatite. The estimated qmax values are 149.25 mg/g, 106.4 mg/g and 147.5 mg/g for the uptake of Zn2+, Co2+, and Cu2+, respectively. Based on monolayer models of one energy and two energies, the number of receptor adsorption sites, number of adsorbed metal ions per active site, the average number of sites which occupied by ions, mono layer adsorption quantity and the adsorption quantity after total saturation were calculated for the first time for such materials.

Photocatalytic removal of Congo red dye using MCM-48/Ni2O3 composite synthesized based on silica gel extracted from rice husk ash; fabrication and application.

MCM-48 mesoporous silica was successfully synthesized from silica gel extracted from rice husk ash and loaded by nickel oxide (Ni2O3). The resulted composite was characterized using X-ray diffraction, scanning electron microscope, and UV-vis spectrophotometer. The role of MCM-48 as catalyst support in enhancing the photocatalytic properties of nickel oxide was evaluated through the photocatalytic degradation of Congo red dye under visible light source. MCM-48 as catalyst support for Ni2O3 shows considerable enhancement in the adsorption capacity by 17% and 29% higher than the adsorption capacity of MCM-48 and Ni2O3, respectively. Additionally, the photocatalytic degradation percentage increased by about 64% relative to the degradation percentage using Ni2O3 as a single component. The adsorption mechanism of MCM-48/Ni2O3 is chemisorption process of multilayer form. The using of MCM-48 as catalyst support for Ni2O3 enhanced the adsorption capacity and the photocatalytic degradation through increasing the surface area and prevents the nickel oxide particles from agglomeration. This was done through fixing nickel oxide particles throughout the porous structure which providing more exposed active adsorption sites and active photocatalyst sites for the incident photons. Based on the obtained results, supporting of nickel oxide particles onto MCM-48 are promising active centers for the degradation of Congo red dye molecules.

Effective retention of cesium ions from aqueous environment using morphologically modified kaolinite nanostructures: experimental and theoretical studies.

Kaolinite can undergo a controlled morphological modification process into exfoliated nanosilicate sheets (EXK) and silicate nanotubes (KNTs). The modified structures were assessed as potential effective adsorbents for the retention of Cs+ ions. The impact of the modification process on the retention properties was assessed based on conventional and advanced equilibrium studies, considering the related steric and energetic functions. The synthetic KNTs exhibit a retention capacity of 249.7 mg g-1 as compared to EXK (199.8 mg g-1), which is significantly higher than raw kaolinite (73.8 mg g-1). The kinetic modeling demonstrates the high effectiveness of the pseudo-first-order kinetic model (R2 > 0.9) to illustrate the sequestration reactions of Cs+ ions by K, EXK, and KNTs. The enhancement effect of the modification processes can be illustrated based on the statistical investigations. The presence of active and vacant receptors enhanced greatly from 19.4 mg g-1 for KA to 40.8 mg g-1 for EXK and 46.9 mg g-1 for KNTs at 298 K. This validates the significant impact of the modification procedures on the specific surface area, reaction interface, and reacting chemical groups' exposure. This also appeared in the enhancement of the reactivity of their surfaces to be able to uptake 10 Cs+ ions by KNTs and 5 ions by EXK as compared to 4 ions by kaolinite. The thermodynamic and energetic parameters (Gaussian energy < 8.6 kJ mol-1; uptake energy < 40 kJ mol-1) show that the physical processes are dominant, which have spontaneous and exothermic properties. The synthetic EXK and KNT structures validate the high elimination performance of the retention of Cs+ either in the existence of additional anions or cations.

Synergetic and advanced isotherm investigation for the enhancement influence of zeolitization and ß-cyclodextrin hybridization on the retention efficiency of U(vi) ions by diatomite.

In synergetic investigations, the adsorption effectiveness of diatomite-based zeolitic structure (ZD) as well as its ß-cyclodextrin (CD) hybrids (CD/ZD) towards uranium ions (U(vi)) was evaluated to examine the influence of the transformation procedures. The retention behaviors and mechanistic processes have been demonstrated through analyzing the steric and energetic factors employing the modern equilibrium approach (a monolayer model with a single energy level). After the saturation phase, the uptake characteristics of U(vi) were dramatically improved to 297.5 mg g-1 after the CD blending procedure versus ZD (262.3 mg g-1) or 127.8 mg g-1. The steric analysis indicated a notable increase in binding site levels after the zeolitization steps (Nm = 85.7 mg g-1) as well as CD implementation (Nm = 91.2 mg g-1). This finding clarifies the reported improvement in the ability of CD/ZD to effectively retain the U(vi) ions. Furthermore, every single active site of the CD/ZD material has the capacity to adsorb around four ions, which are aligned according to a vertical pattern. The energetic aspects, specifically Gaussian energy (<8 kJ mol-1) along with retention energy (<40 kJ mol-1), validate the regulated influences of the physical mechanistic processes. The physical adsorption of U(vi) seems to depend on various intermolecular forces, such as van der Waals forces, in conjunction with zeolitic ion exchanging pathways (0.6-25 kJ mol-1). The thermodynamic assets have been evaluated to confirm the exothermic together with spontaneous adsorption U(vi) by ZD and its blend with CD (CD/ZD).

Enhanced Retention of Cd(II) by Exfoliated Bentonite and Its Methoxy Form: Steric and Energetic Studies.

Synergistic studies were conducted to evaluate the retention potentiality of exfoliating bentonite (EXBEN) as well as its methanol hybridization derivative (Mth/EXBEN) toward Cd(II) ions to be able to verify the effects of the transformation processes. The adsorption characteristics were established by considering the steric and energetic aspects of the implemented advanced equilibrium simulation, specifically the monolayer model with a single energy level. Throughout the full saturation states, the adsorption characteristics of Cd(II) increased substantially to 363.7 mg/g following the methanol hybridized treatment in comparison to EXBEN (293.2 mg/g) as well as raw bentonite (BEN) (187.3 mg/g). The steric analysis indicated a significant rise in the levels of the active sites following the exfoliation procedure [retention site density (Nm) = 162.96 mg/g] and the chemical modification with methanol [retention site density (Nm) = 157.1 mg/g]. These findings clarify the improvement in the potential of Mth/EXBEN to eliminate Cd(II). Furthermore, each open site of Mth/EXBEN has the capacity to bind approximately three ions of Cd(II) in a vertically aligned manner. The energetic investigations, encompassing the Gaussian energy (less than 8 kJ/mol) plus the adsorption energy (less than 40 kJ/mol), provide evidence of the physical sequestration of Cd(II). This process may involve the collaborative impacts of dipole binding forces (ranging from 2 to 29 kJ/mol) and hydrogen binding (less than 30 kJ/mol). The measurable thermodynamic functions, particularly entropy, internal energy, and free enthalpy, corroborate the exothermic and spontaneous nature of Cd(II) retention by Mth/EXBEN, as opposed to those by EXBEN and BE.