Surface Pore Research Articles

Long-wave instabilities of a power-law fluid flowing over a heated, uneven and porous incline: A two-sided model

The stability conditions of a two-dimensional gravity-driven flow of a thin layer of a power-law fluid flowing over a heated, uneven, inclined porous surface are investigated. A two-sided model is employed to account for the bottom filtration in the porous layer. The governing equations are reduced under the long-wave approximation and the cross-stream dependence is eliminated by means of the Integral Boundary Layer technique. Floquet–Bloch theory is used to investigate at linear level how the porous bottom waviness influences the thermocapillarity stability of the flow in a shear-thinning fluid. Differently from the even case, the linear stability analysis suggests that for flow over sufficiently wavy undulations the thermocapillarity may stabilize the equilibrium flow, depending on the values of dimensionless governing numbers and parameters. This stabilizing phenomenon is enhanced by the shear-thinning rheology of the fluid while it is reduced by the permeability of the layer. Numerical simulations, performed solving the reduced nonlinear model through a second order Finite Volume scheme, confirm the results of the linear stability analysis.

Adsorption simulation of 2,4-D pesticide on novel zinc-based 2-amino-4-(1H-1,2,4-triazole-4-yl)benzoic acid coordination complexes using machine learning approach.

The capacity of zinc-based 2-amino-4-(1H-1,2,4-triazole-4-yl)benzoic acid coordination complex (Zn(NH2-TBA)2) and modified Zn(NH-TBA)2COMe complex for removal of 2,4-dichlorophenoxyacetic acid (2,4-D) from aqueous solutions was investigated through adsorption modeling and artificial intelligence tools. Analyzing the adsorption characteristics of pesticides helps in studying the groundwater pollution by pesticides in agriculture area.In this study, Zn(NH2-TBA)2 was synthesized using Schiff base and its surface was modified using acetic anhydride group and their physical characteristics were identified using proton NMR, FTIR, and XRD. NMR results showed maximum modification yield obtained was 65% after 5days. The porous structure and surface area monitored using nitrogen isotherm and BET surface area analysis presented relatively less surface area and porosity after modification. Adsorption modelling indicated that Toth model with a maximum adsorption capacity of 150.8mg/g and 100.7mg/g represents the homogenous adsorption systems which satisfy both low- and high-end boundary of adsorbate concentration in all settings according to the optimum point, while the kinetics and rate of 2,4-D adsorption follow the pseudo-first-order kinetic model in all situations. Artificial neural network (ANN), support vector regression, and particle swarm optimized least squares-support vector regression (PSO-LSSVR) were used for the optimization and modelling of adsorbent mass, adsorbate concentration, contact time, and temperature to develop predictive equations for the simulation of the adsorption efficiency of 2,4-D pesticide. The obtained results exhibited the better performance of ANN and PSO-LSSVR for prediction of adsorption results. The mean square error values of ANN (0.001, 0.012) and PSO-LSSVR (0.121, 0.105) were obtained for Zn(NH2-TBA)2 and Zn(NH-TBA)2COMe, respectively, while their respective coefficient of determination (R2) obtained were 0.999 and 0.988 for ANN and 0.980 and 0.825 for PSO-LSSVR. The study specified that machine learning predictive behavior performed better for Zn(NH2-TBA)2 compared to Zn(NH-TBA)2COMe that is also supported by theoretical kinetics and isotherm models. The research concludes that artificial intelligence models are the most efficient tools for studying the predictive behavior of adsorption data.

Nitrogen-doped porous carbon with regulated pore structure and surface wettability as flow electrodes for efficient capacitive deionization

Nitrogen-doped porous carbon with controlled pore structure and wettability was synthesized using spent mushroom substrate (SMS) via physical activation process. The nitrogen-rich feature of precursor enables the carbon material to possess both electrical conductivity and surface wettability, creating an effective conducting network in flow electrodes. These materials have been proven to be highly efficient for deionization due to their ability of maintaining surface wettability and electrical conductivity. Our results show that the SMS-1.5 sample has a high adsorption capacity of 8.38 mg/g, which is 1.8 times greater than the commercial YP-50. The corresponding charge efficiency was up to 90.66 % after being exposed to 1.6 g/L NaCl feed solution for 120 min in flow electrode capacitive deionization device. This study highlights the significance of the inherent nitrogen element in biomass for the synergistic promotion of electrical conductivity and surface wettability, providing a strategy for designing porous carbons with excellent desalination performance.

Enhanced removal of ciprofloxacin and associated antibiotic-resistant genes from wastewater using a biological aeration filters in combination with Fe3O4-modified zeolite.

Antibiotics release into the water environment through sewage discharge is a significant environmental concern. In the present study, we investigated the removal of ciprofloxacin (CIP) in simulated sewage by biological aeration filter (BAF) equipped with Fe3O4-modified zeolite (Fe3O4@ZF). Fe3O4@ZF were prepared with impregnation method, and the Fe3O4 particles were successfully deposited on the surface of ZF in an amorphous form according to the results of XPS and XRD analysis. The modification also increased the specific surface area (from 16.22 m²/g to 22 m²/g) and pore volume (from 0.0047 cm³/g to 0.0063 cm³/g), improving the adsorption efficiency of antibiotics. Fe3O4 modified ZF improved the treatment performance significantly, and the removal efficiency of CIP in BAF-Fe3O4@ZF was 79%±2.4%. At 10ml/L CIP, the BAF-Fe3O4@ZF reduced the relative abundances of antibiotics resistance genes (ARGs) int, mexA, qnrB and qnrS in the effluent by 57.16%, 39.59%, 60.22%, and 20.25%, respectively, which effectively mitigate the dissemination risk of ARGs. The modification of ZF increased CIP-degrading bacteria abundance, such as Rhizobium and Deinococcus-Thermus, and doubled bacterial ATP activity, promoting CIP degradation. This study offers a viable, efficient method to enhance antibiotic treatment and prevent leakage via sewage discharge.

Poly[1-vinyl-3-benzyltriethylammonium proline ionic liquid] membrane: Preparation, properties and adsorption applications

A novel poly[1-vinyl-3-benzyltriethylammonium proline ionic liquid] membrane(PIL/PVDF membrane) were prepared through the blending poly[1-vinyl-3-benzyltriethylammonium proline ionic liquid](P[Pro][TEA])-poly(vinylidene fluoride)(PVDF) phase inversion method. A series of PIL/PVDF membrane characterization (NMR, FT-IR, SEM, EDS, and XPS) was performed. The properties of PIL/PVDF membrane (contact angle, water flux, mechanical properties, thermal stability,electric charge property, specific surface area and pore diameter) were evaluated. A solid phase extraction − high performance liquid chromatography (SPE-HPLC) method for separation/analysis of quercetin was developed. The factors affecting the adsorption and elution (time, dosage, pH etc.) were investigated. Under optimal conditions, the method has been successfully applied to the separation/analysis of quercetin in tea, and the recovery rates are satisfactory (86.4–106.0 %). The concentration factor of quercetin was 10. The adsorption capacity of PIL/PVDF membrane towards quercetin was 22.1 mg g−1. The extraction mechanism was preliminarily discussed. The established SPE-HPLC method was simple and reliable, which provided application prospects for extraction and detection of quercetin.

Hydrothermal synthesis of high crystallinity ZSM-5 zeolite from coal gasification coarse slag and mother liquor circulation for efficient coal chemical wastewater purification.

A hydrothermal synthesis method was developed to produce high crystallinity ZSM-5 zeolite using coal gasification coarse slag (CGCS) as the raw material. Instead of the expensive NaOH(s.), Na2SiO3(s.) was utilized to activate, depolymerize, and recombine Si and Al elements in the CGCS. The mother liquor circulation technology was employed to recover and reuse raw materials and residual reagents (Na2SiO3(aq.) and TPABr), reducing waste emissions and enhancing resource utilization efficiency. The synthesized ZSM-5 had a specific surface area of 455.675 m2g-1, pore volume of 0.284 cm3g-1, and pore diameter of 2.496nm. The influence of various factors on the morphology and crystallinity of ZSM-5 was investigated, resulting in the production of ZSM-5 with higher specific surface area and pore volume. Adsorption experiments showed that WU-ZSM-5 exhibited a removal efficiency of 85% for ammonia nitrogen (NH4+-N(aq.)), validating its effectiveness in coal chemical wastewater purification. The mother liquor recycling technology enabled zero-emission utilization of solid waste resources and improved the utilization rate of alkali and template to 90%. These results demonstrate the potential application of the developed method in the efficient treatment of coal chemical wastewater.

Modelling the far-field effect of drag-induced dissipation in wave–structure interaction: a numerical and experimental study

In the interaction of water waves with marine structures, the interplay between wave diffraction and drag-induced dissipation is seldom, if ever, considered. In particular, linear hydrodynamic models, and extensions thereof through the addition of a quadratic force term, do not represent the change in amplitude of the waves diffracted and radiated to the far field, which should result from local energy dissipation in the vicinity of the structure. In this work, a series of wave flume experiments is carried out, whereby waves of increasing amplitude impinge upon a vertical barrier, extending partway through the flume width. As the wave amplitude increases, the effect of drag – which is known to increase quadratically with the flow velocity – is enhanced, thus allowing the examination of the far-field effect of drag-induced dissipation, in terms of wave reflection and transmission. A potential flow model is proposed, with a simple quadratic pressure drop condition through a virtual porous surface, located on the sides of the barrier (where dissipation occurs). Experimental results confirm that drag-induced dissipation has a marked effect on the diffracted flow, i.e. on wave reflection and transmission, which is appropriately captured in the proposed model. Conversely, when diffraction becomes dominant as the barrier width becomes comparable to the incoming wavelength, the diffracted flow must be accounted for in predicting drag-induced forces and dissipation.

Preparation and characterization of AChE immobilized magnetic bio-nanocomposites (Fe3O4@Cht/Au) for pesticide detection

Free enzymes cause difficulties in many applications due to their insufficient stability, loss of activity in a short time, and most importantly, although they are costly, they are used only once in reactions, lose their effect and cannot be recovered from the environment. Magnetic nanoparticles coated with biocompatible polymeric material are potential candidates for promising enzyme carriers due to their multifunctional pore surfaces, easy removal from the environment provided by the magnetization, ability to main stability under various harsh conditions. This study prepared a biosensor candidate based on the inhibiting acetylcholinesterase enzyme by organophosphate pesticides from chitosan-coated magnetic nanoparticles doped with gold. Transmission electron microscopy, scanning electron microscopy, X-ray diffraction diffractometry, and Fourier transform infrared spectroscopy analysis confirmed the structure of synthesized nanocomposites. Magnetic characteristics of the nanocomposites were assessed using VSM. Bio-nanocomposite (Fe3O4@Cht/Au/AChE) was used to determine environmental pollutants qualitatively. Remediation of organophosphate-containing wastewater is an essential issue for environmental sustainability. In this work, Dichlorvos and Chlorpyrifos were selected as organic pollutants to assess the enzymatic activity of immobilized Fe3O4@Cht/Au/AChE. Optimum conditions for AChE enzyme were immobilized nanostructures (Fe3O4@Cht/Au/AChE) were determined. The optimum pH for the immobilized enzyme was found to be 8, and the optimum temperature was found to be 60 °C. Retained immobilized enzyme activity is found to be around 50% for the 20th reuse. In the presence of 150 µL pesticide, retained immobilized enzyme activity is found to be around 25%. Method validation was performed for pesticides. When using immobilized AChE, the LOD (limit of detection)-LOQ (limit of quantitation) values for Dichlorovos and Chlorpyrifos was obtained in the range of 0.0087–0.029 nM and 0.0014–0.0046 nM, respectively. The relative standard deviation (RSD%) values, which are indicators of precision, were found to be below 2%.

Single-Pore Nanofluidic Logic Memristor with Reconfigurable Synaptic Functions and Designable Combinations.

The biological neural network is a highly efficient in-memory computing system that integrates memory and logical computing functions within synapses. Moreover, reconfiguration by environmental chemical signals endows biological neural networks with dynamic multifunctions and enhanced efficiency. Nanofluidic memristors have emerged as promising candidates for mimicking synaptic functions, owing to their similarity to synapses in the underlying mechanisms of ion signaling in ion channels. However, realizing chemical signal-modulated logic functions in nanofluidic memristors, which is the basis for brain-like computing applications, remains unachieved. Here, we report a single-pore nanofluidic logic memristor with reconfigurable logic functions. Based on the different degrees of protonation and deprotonation of functional groups on the inner surface of the single pore, the modulation of the memristors and the reconfiguration of logic functions are realized. More noteworthy, this single-pore nanofluidic memristor can not only avoid the average effects in multipore but also act as a fundamental component in constructing complex neural networks through series and parallel circuits, which lays the groundwork for future artificial nanofluidic neural networks. The implementation of dynamic synaptic functions, modulation of logic gates by chemical signals, and diverse combinations in single-pore nanofluidic memristors opens up new possibilities for their applications in brain-inspired computing.

MgBu2 nanosheets encapsulated in ZIF-8 for producing carbon scaffold in situ nanoconfined Mg hydrogen storage materials: Record-high loading and decreased dehydrogenation enthalpy

Nanoconfinement is an effective strategy to improve the kinetic and thermodynamic properties of the Mg/MgH2 system. However, current nanoconfinement approaches including porous scaffolds impregnation and surface anchoring can hardly obtain high loading, agglomeration resistant, and air-stable Mg nanoparticles. Herein, we report a novel strategy for preparing carbon scaffold in situ nanoconfined Mg hydrogen storage materials. The 12.2 nm MgBu2 nanosheets precipitated by solvent displacement are encapsulated in ZIF-8 to prepare MgBu2@ZIF-8, which are then pyrolyzed at 800°C to obtain Mg@C nanocomposites with 8.7 nm Mg embedded in a carbon scaffold. First principles calculations have demonstrated that the addition of MgBu2 promotes the nucleation and growth of ZIF-8 to form MgBu2@ZIF-8. It is worth noting that the loading rate of Mg@C-3 sample reaches a record high of 76.3% and exhibits outstanding hydrogen storage performances. Surprisingly, the enthalpy of hydrogen absorption/desorption sharply decreases to −62.0/63.1 kJ mol−1 H2. Mg@C-3 can absorb 4.4 wt% H2 at 200°C and desorb 4.0 wt% H2 at 250°C, and the activation energy for hydrogen absorption/desorption is reduced to a staggering 53.1/74.2 kJ mol−1 H2. Moreover, Mg@C-3 shows high cycling stability and antioxidant performance. This work opens a novel approach for the development of nanoconfined Mg nanocomposites with excellent performances.

Modification of new magnetic nanocomposites Bi2WO6/CuFe2O4 and its excellent catalytic reduction for toxic nitroaromatic compounds and chromium (VI)

New magnetic Bi2WO6/CuFe2O4 nanocomposites were synthesized using hydrothermal method. The specific features of Bi2WO6/CuFe2O4 nanocomposites were studied using various analytical techniques such as Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM) and N2 adsorption desorption analyses, Brunauer-Emmett-Teller (BET). The BET analysis demonstrates that embedded CuFe2O4 nanoparticles in Bi2WO6 structure have increased the pore diameters and surface area for better adsorption of NaBH4 and catalytic performance. The VSM analysis confirms the magnetic behavior of nanocomposite which showed that Bi2WO6/CuFe2O4 could be separated and recoverd easily by an external magnet after catalytic reactions. The catalytic performance of nanocomposites was investigated for the reduction of nitroaromatic compounds including 4-nitroaniline (4-NA), 4-nitrophenol (4-NP), 2-nitroaniline (2-NA) and 2-nitrophenol (2-NP) and chromium (VI) in aqueous solution. The results show the nanocomposites have excellent ability to reduces Cr(VI) to Cr(III) and nitroaromatic compounds to the corresponding amines in green water solution at room temperature. The best performance observed for the 100% conversion of 4-nitrophenol reduction belongs to Bi2WO6/CuFe2O4 20%, which completes in 6 min, and its rate constant is about 0.67 min−1. In addition, the Bi2WO6/CuFe2O4 nanocomposite can be appropriately recycled and reused several times without changing its structure and activity, which is essential for practical applications.

Designing P-doped graphite-like hierarchical porous carbon nanosheets from coal tar pitch for enhanced Zn-ion hybrid capacitors

The innovative design of pitch-based carbon cathodes holds profound implications for optimizing the efficient utilization of coal tar pitch (CTP) and hastening the progress of Zn-ion hybrid capacitors (ZIHCs). Herein, P-doped graphite-like porous carbon nanosheets (PGCNs) were designed by cleverly combining pre-oxidation, catalytic graphitization, and H3PO4 modification. Throughout oxidation, adjustments were made to the surface functional groups and molecular sizes of CTP to ensure subsequent catalytic and activation effects. Then a uniform lamellar structure and highly graphitized porous carbon matrix were successfully generated through catalytic graphitization. The pore structure and surface chemical properties were further enhanced through H3PO4 modification. When PGCNs were integrated into ZIHCs, the assembled Zn//PGCNs device demonstrated a specific capacity of 133.2 mAh/g at 1 A/g, an energy density of 113.8 Wh/kg at 404.7 W/kg, and maintained a cycle stability of 90.6% after 10,000 cycles.

CO2-triggered (3-aminopropyl)triethoxysilane-functionalized M-MOF-74 stabilized Pickering emulsions

Pickering emulsions with a stimulus response have been paid extensive concern due to their long-term stability and demulsification on-command. Metal-organic frameworks (MOFs) are expectable emulsifying agents to build Pickering emulsions based on their excellent properties such as high specific surface area, adjustable porosity and pore size. Herein, a novel kind of CO2-triggered Pickering emulsions formed by (3-aminopropyl)triethoxysilane (APTES)-functionalized M-MOF-74 (M-MOF-74-APTES, M = Zn, Cu or Mg) has been developed for the first time. It was found that even at the M-MOF-74-APTES amount of 0.5 wt%, the functionalized MOFs could still stabilize the n-hexane-watermixture to construct Pickering emulsions. The as-generated Pickering emulsions could be efficiently demulsified upon bubbling of CO2, resulting in complete separation of oil and water phases, but could be restored by subsequent N2 bubbling under homogenization. Mechanism study indicated that the acid-base reaction of CO2 with the amino group of M-MOF-74-APTES resulted in the creation of hydrophilic salts, which led to the lowering of particle wettability and broke the stability of the emulsion, causing demulsification of the Pickering emulsion. After removing CO2, the emulsion can be reconstructed by the reversible reaction. As an applied example, the Pickering emulsion has been availed as a micro-reaction system and M-MOF-74-APTES as a carrier of Pd(OAc)2 catalyst to realize the efficient combination of Suzuki-Miyaura reaction, product isolation and reuse of catalysts via alternate bubbling or removing of CO2.

A novel biochar-based 3D composite for ultrafast and selective Cr(VI) removal in electroplating wastewater

In this study, a newly developed composite of biochar-poly(m-phenylenediamine) (BC-PmPD) exhibiting a distinct skeletal structure was synthesized for the purpose of extracting Cr(VI) from aqueous solutions. BC was employed as a supportive carrier onto which PmPD nanoparticles were uniformly affixed through in-situ polymerization and oxidation synthesis, both within and outside the layered configuration of BC. The structural stability and morphologies of BC-PmPD were assessed utilizing Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy, thermogravimetric analysis, analysis of specific surface area and pore size, X-ray photoelectron spectroscopy (XPS), and X-ray diffraction. In comparison to other modified BCs reported, BC-PmPD exhibited the highest Cr(VI) removal rate. Specifically, at 303 K, BC-PmPD achieved a maximum Cr(VI) removal capacity of 775 mg g−1, surpassing the capabilities of unmodified BC and PmPD by 10.4 and 2.13 times, respectively. Analyses involving XPS, FTIR, and density functional theory calculation confirmed that proton transfer happened between protonated amine (−NH2) functional group within the structure of BC-PmPD and HCrO4− before the formation of hydrogen bond. Subsequently, environmentally persistent free radicals facilitated the reduction of the adsorbed Cr(VI). Quantification of the functional groups indicated that the amino group was responsible for 93.0% of the Cr(VI) adsorption in BC-PmPD. BC-PmPD displayed potent adsorption and reduction capabilities, alongside notable stability, repeatability, and promising potential for application in the remediation for high concentrations of Cr(VI) in electroplating wastewater scenarios.Graphical

Thermal radiation and soret/dufour effects on amplitude and oscillating frequency of darcian mixed convective heat and mass rate of nanofluid along porous plate

The influence of thermal radiations and Soret/Dufour significantly increases the mass and heat transport in material science, geothermal process, chemical rectors and heat exchangers due to temperature and concentration variation of nanoparticles. Main objective is to enhance the amplitude, oscillation and frequency of heat transfer using the Soret and Dufour characteristics in Darcian radiating flow of thermophoretic nanoparticles along vertical porous surface. The dimensionless analysis is performed to develop the convenient form of governing thermodynamic Darcian nanofluid formulation. To develop the programming algorithm in FORTRAN language, the primitive variable formulation is used for both time-dependent and steady models. The numerical and graphical outcomes of primitive type equations under boundary conditions are explored by using implicit finite difference approach with Gaussian elimination scheme. Various pertinent parameters are used to elaborate the steady fluid velocity, surface temperature and steady concentrated nanoparticle volume fraction. Valuable novelty of current research is to use steady results for fluctuating shear stress, fluctuation heating rate and fluctuating mass rate. It is found that the influence of Soret and Dufour parameter enhances the fluid velocity and temperature distribution with maximum variations. It is noticed that the temperature distribution enhances as thermal radiation parameter increases. The oscillation and transient stability of heating rate enhances with prominent variations as thermal radiation and Soret/Dufour parameter increases. It is depicted that amplitude in shear stress and mass rate enhances as Soret and Dufour parameter enhances.

Synthesis of microporous titanium surface with aligned pores through changes of currents during electrochemical process

This paper reports the synthesis of microporous Ti surfaces with aligned pores by applying a different current during electrochemical process for application in cell-surface interaction study and biomedical implants. As the microporous Ti surfaces were synthesized by current from (0.5–4)A, the microstructure of the Ti surfaces was shifted from a relative smooth to microporous one that was observed to have an aligned pore surface. Optical images showed that the micropore sizes in ∼(85.4–224.4)µm. The roughness of the microporous Ti was significantly higher than that of the Ti by a factor of approximately 5 to 7. Confocal laser scanning microscope showed excellent cell attachment and preferential growth on the microporous Ti with aligned channels after 72 h of culturing which could be important for cell-surface interactions study and biomedical implants.

Indicative significance of the interfacial interactions between pore surface and soluble organic matter on the shale oil mobility

The exploration and exploitation of shale oil resources enhance the necessity to characterize the mobility of the occluded oil in shales. Up to now, the understanding of the controlling factors of shale oil mobility has mainly come from molecular dynamics simulation but lacking in-depth research on actual shales. Therefore, in this study, the effects of mineral composition, soluble organic matter (SOM) composition and wettability on the shale oil mobility were studied by X-ray diffraction, N2 adsorption, mercury intrusion, contact angle, chloroform bitumen and group component detection methods, comprehensively. The results show that: (1) The asphaltene contents and (Asphaltenes × Aromatics)/(Saturates × Resins) negatively and positively correlate with clay and carbonate mineral contents, respectively, while the I/S and illite contents present opposite trend with (Asphaltenes × Aromatics)/(Saturates × Resins). These correlations indicate that the SOM that confined in the pores constructed with carbonate minerals and illite present better flow potential. (2) Both δVt and δSSA negatively correlate with asphaltenes and (Asphaltenes × Aromatics)/(Saturates × Resins). That is, less pores and surfaces can be released by extraction for the shales with more asphaltenes. Therefore, it can be concluded that asphaltene is a negative factor for shale oil seepage. Additionally, the larger pores present better flow condition for shale oil, even for asphaltenes. (3) Pore surface wettability also significantly affects the shale oil mobility. The hydrophobicity of the pore wall greatly inhibits the shale oil flow, especially for the mesopores and macropores. The pattern diagram was established to illustrate the effect of the interactions between pore surfaces and shale oil components on the movable potential. Based on our research, mineral composition, group composition and pore surface wettability are efficient parameters for the shale oil mobility evaluation based on the interfacial interaction theory, and the “sweet spots” for shale oil seepage of the Jiyang Depression are the shales with more illite, carbonate, saturates and relatively low lipophilicity.

Synthesis, characterisation and application of organic and inorganic bentonite for the removal of gentian violet

ABSTRACT The intensive use of dyes in industry has caused serious pollution problems, due to industrial wastewater discharges. It is well known that dyes have harmful effects on humans, animals, and other living beings. Therefore, the treatment of industrial wastewater before its release into the environment requires great attention. This work is devoted to the study of the effect of organic modifications by DMSO and/or CTAB and an inorganic modification by spinel oxide ZnCr2O4 on the structural and textural properties of local clay (M’Zila bentonite). The materials resulting from these modifications are used as adsorbents for a cationic dye such as gentian violet. These materials were synthesised and characterised by XRD, FTIR, BET and SEM. These analyzes confirmed the considerable changes in the structure of the clays modified by DMSO and/or CTAB- ZnCr2O4, the formation of pillared bentonites and the increase in the basal spacing’s of the modified clays by 15.05 Å for the bentonite of M’Zila at 23.80 Å for bentonite-CTAB-ZnCr2O4 (BCZnCr), at 27.37 Å for bentonite-DMSO-ZnCr2O4 (BDZnCr) and at 25.89 Å for bentonite-DMSO-CTAB-ZnCr2O4 (BDCZnCr).These modifications produced a rougher and more porous surface, resulting in a significant increase in the specific surface area from 60.13 m2 g−1 for sodium bentonite to 104.63 m2 g−1 for BCZnCr and 104.59 m2 g−1 for BDCZnCr. The adsorption of gentian violet was carried out under the following conditions: solid liquid ratio: 1 g/L, pH = 10 and contact time at equilibrium 1 h. The adsorption kinetics perfectly follows the pseudo second order model as well as that of intraparticle diffusion for all materials. The isotherms are of type S; they are well described by the Langmuir-Freundlich model. The thermodynamic parameters indicate that the physisorption of gentian violet by the different materials is spontaneous, exothermic, and disordered.

Hexavalent chromium adsorption from aqueous solution utilizing activated carbon developed from Rumex abyssinicus

The indiscriminate release of chromium-saturated effluent into water bodies has raised concerns regarding its effect on human health and environmental ecology. Therefore, this research aimed to remove hexavalent chromium from an aqueous solution utilizing activated carbon developed from Rumex abyssinicus. The adsorbent was prepared through chemical impregnation with H3PO4 and then thermally activated at 500 °C for 2 h. The optimization of the adsorption experiments was performed using the Box‒Behnken approach of response surface methodology. The characterization of the prepared activated carbon revealed good quality in terms of its amorphous structure, maximum specific surface area of 1722.9 m2/g and porous surface. Furthermore, the optimization results showed that a maximum removal efficiency of 95.97 % was attained at an optimum working pH of 3, a contact time of 60 min, an initial chromium concentration of 70 mg/L and an adsorbent dosage of 0.6 mg/100 mL. The Langmuir isotherm model was found to have the best fit with the experimental data. Moreover, the kinetics study revealed that a pseudo-second-order model fit the data best, indicating the occurrence of chemisorption. Overall, this study suggested that Rumex abyssinicus could be an effective adsorbent for removing hexavalent chromium from aqueous solutions.

Cross-Linking CdSO4-Type Nets with Hexafluorosilicate Anions to Form an Ultramicroporous Material for Efficient C2H2/CO2 and C2H2/C2H4 Separation.

A 44.610.8 topology hybrid ultramicroporous material (HUM), {[Cu1.5F(SiF6)(L)2.5]·G}n, (L = 4,4'-bisimidazolylbiphenyl, G = guest molecules), 1, formed by cross-linking interpenetrated 3D four-connected CdSO4-type nets with hexafluorosilicate anions is synthesized and evaluated in the context of gas sorption and separation herein. 1 is the first HUM functionalized with two different types of fluorinated sites (SiF6 2- and F- anions) lining along the pore surface. The optimal pore size (≈5Å) combining mixed and high-density electronegative fluorinated sites enable 1 to preferentially adsorb C2H2 over CO2 and C2H4 by hydrogen bonding interactions with a high C2H2 isosteric heat of adsorption (Qst) of ≈42.3kJmol-1 at zero loading. The pronounced discriminatory sorption behaviors lead to excellent separation performance for C2H2/CO2 and C2H2/C2H4 that surpasses many well-known sorbents. Dynamic breakthrough experiments are conducted to confirm the practical separation capability of 1, which reveal an impressive separation factor of 6.1 for equimolar C2H2/CO2 mixture. Furthermore, molecular simulation and density functional theory (DFT) calculations validate the strong binding of C2H2 stems from the chelating fix of C2H2 between SiF6 2- anion and coordinated F- anion.