Specific Surface Area Values Research Articles

Highlighting the adsorption mechanism of a fluoroquinolone antibiotic from wastewater on carbon xerogel by experiments, characterization, modelling and DFT simulation.

The application of a synthesized carbon xerogel (RFX) for the adsorptive removal from water of ciprofloxacin (CPX), a widely used fluoroquinolones-group antibiotic for humans and animals, has been reported in this work. The carbon xerogel was characterized by N2 adsorption-desorption isotherms, FTIR, Raman spectroscopy, TPD studies, elemental analysis, determination of isoelectric point (pHIEP) and scanning electron microscopy (SEM). CPX adsorption experiments were conducted in batch mode, using results obtained with F400 commercial activated carbon for comparison purposes. CPX adsorption kinetics were well-described by the pseudo-second-order model for both adsorbents and by the Elovich model in the case of F400 activated carbon. Therefore, CPX equilibrium adsorption capacity values were of 457 and 72mgg-1 for RFX xerogel and F400 activated carbon, respectively. This significant difference can be attributed to the higher specific surface area and micropores volume values of F400 carbon; in this sense, this material led to a slower CPX kinetic adsorption. Also, the Dual-site Langmuir model best-described the experimental CPX adsorption isotherms in both cases. By the adsorption studies at different solution pH, it could be concluded that several mechanisms, e.g., hydrophobic and π-π interactions, and electrostatic forces highly influenced CPX adsorption capacity. Furthermore, adsorption tests using several environmentally relevant aqueous matrices have been accomplished. In this case, a competitive effect between the natural organic matter (NOM) and the target pollutant occurred in all the tested real matrices, decreasing CPX adsorption capacity, especially remarkable for F400 activated carbon. Finally, Density Functional Theory (DFT) has been used to elucidate the interactions between CPX and adsorbents, finding a high relevance of the π-π electron donor-acceptor interactions in which CPX acts as an acceptor.

Regeneration and Single Stage Batch Adsorber Design for Efficient Basic Blue-41 Dye Removal by Porous Clay Heterostructures Prepared from Al13 Montmorillonite and Pillared Derivatives.

Porous clay heterostructures are a hybrid precursor between the pillaring process and organoclays. In this study, the organoclay was substituted by an aluminium intercalated species clay or pillared alumina clays. A porous clay heterostructure was successfully achieved from an aluminium intercalated species clay, due to the easy exchange of the aluminium species by the cosurfactant and silica species. However, using alumina pillared clays, the porous clay heterostructures were not formed; the alumina species were strongly attached to clay sheets which made difficult their exchange with cosurfactant molecules. In this case, the silica species were polymerized and decorated the surface of the used materials as indicated by different characterization techniques. The specific surface area of the porous clay heterostructure material reached 880 m2/g, and total pore volume of 0.258 cc/g, while the decorated silica alumina pillared clays exhibited lower specific surface area values of 244-440 m2/g and total pore volume of 0.315 to 0.157 cc/g. The potential of the synthesized materials was evaluated as a basic blue-41 dye removal agent. Porous clay heterostructure material has a removal capacity of 279 mg/g; while the other materials exhibited lower removal capacities between 75 mg/g and 165 mg/g. The used regeneration method was related to the acidity of the studied materials. The acidity of the materials possessed an impact on the adopted regeneration procedure in this study, the removal efficiency was maintained at 80% of the original performance after three successive regeneration cycles for the porous clay heterostructure. The Langmuir isotherm characteristics were used to propose a single-stage batch design. Porous clay heterostructures with a higher removal capacity resulted in a decrease in the quantities needed to achieve the target removal percentage of the BB-41 dye from an aqueous solution.

Optimized pyrolytic synthesis and physicochemical characterization of date palm seed biochar: unveiling a sustainable adsorbent for environmental remediation applications.

This study focuses on the optimization and comprehensive characterization of biochar synthesized from date palm seeds (DPS), a prevalent agricultural waste in arid regions. Using response surface methodology (RSM) with a central composite design (CCD), we optimized the pyrolysis process by investigating the effects of time (1-3 h) and temperature (600-900 °C) on critical properties such as specific surface area, pore volume, and yield. The optimized biochar, produced at 828 °C for 1.7 h, demonstrated a high specific surface area of 654.8 m2/g and well-developed microporosity. Characterization techniques, including XRD, FTIR, SEM-EDS, and BET analyses, revealed an amorphous carbon structure with graphitic domains, diverse surface functionalities, and a heterogeneous porous microstructure. The biochar's point of zero charge at pH 7.58 indicates its potential for selective adsorption of charged contaminants. The close agreement between RSM-predicted and experimental values for specific surface area (652.1 m2/g vs. 654.8 m2/g) and micropore volume (0.191 cm3/g vs. 0.190 cm3/g) validates the effectiveness of the model in optimizing biochar properties. This research highlights the potential of DPS-derived biochar as a sustainable adsorbent for environmental remediation, opening avenues for valorizing agricultural wastes and contributing to circular economy principles.

Physical–Chemical and Thermal Properties of Clays from Porto Santo Island, Portugal

The use of clays for thermal treatments and cosmetic purposes continues to be a worldwide practice, whether through the preservation of native cultural traditions, pharmaceutical formulations or integrative health and well-being practices. Special clays, such as bentonites, are very common for healing applications due to their high cation exchange capacity (CEC), high specific surface area (SSA) and alkaline pH values and, therefore, are used in multiple therapeutic and dermocosmetic treatments. Numerous bentonitic deposits occur on Porto Santo Island with different chemical weathering degrees. This research evaluates which residual soils have the most suitable characteristics for pelotherapy. The texture of residual soils varies from silt loam to loamy sand and SSA between 39 and 90 m2/g. The pH is alkaline (8.7 to 9.6), electrical conductivity ranges from 242 to 972 µS/cm, and CEC from 50.4 to 86.8 µS/cm. The residual soils have a siliciclastic composition (41.36 to 54.02% SiO2), between 12.52 and 17.65% Al2O3 and between 52 and 82% smectite content, which are montmorillonite and nontronite. Specific heat capacity (0.5–0.9 J/g°C) and cooling kinetics (14.5–19 min) show that one residual soil has the potential to be suitable for pelotherapy according to the literature. Moreover, the residual soils have As, Cd, Co, Cr, Hg, Mn, Ni, Pb, Sb and V concentrations higher than the limits of guidelines for cosmetics and pharmaceutical products.

MnO2-decorated flexible carbon nanofibers with controllable hierarchical porous nanostructures for high energy density supercapacitors

Constructing hierarchical porous structures and reducing material size enhance the electrochemical efficiency of porous carbon-based electrodes. In this study, ultrafine hierarchical porous carbon-based nanofibers were synthesized via electrospinning a blend of polyacrylonitrile, polymethyl methacrylate (PMMA), and zinc acetate dihydrate (ZAH), followed by pre-oxidation, carbonization, and acid washing. Adjusting the ZAH content allowed precise control of fiber diameters (300-600nm) and promoted significant hierarchical porous structures, achieving an optimal mesopore to micropore ratio (1.65) and a high specific surface area (SSA) of 599 m²/g. MnO2 nanosheets were in-situ modified on the carbon nanofibers, forming a hybrid electrode (MnO2@HPCNFs) with excellent flexibility, high SSA value, and rich pore structure. This electrode demonstrated a specific capacitance value equal to 1035 F/g at 0.5 A/g and maintained 80.7% capacitance at 10 A/g. The assembled asymmetric supercapacitor achieved an energy density of 54.81 Wh/kg. This study presents new possibilities for binder-free, self-supporting electrodes in electrochemical energy storage devices.

Biomorphic porous ceramics obtained by infiltration of a Si-based preceramic polymer into poplar wood templates

In this work, a comprehensive and detailed study about the development and characterization of biomorphic porous SiOC/SiC/Si3N4/C-based ceramics was addressed with an integral approach. The materials were obtained using a novel processing route involving the infiltration of a Si-based preceramic polymer into activated poplar wood templates, thermal curing and N2 pyrolysis. The physical, structural, microstructural, and textural properties mostly depended on the degree of infiltration reached and the pyrolysis temperature used. All the developed porous microstructures exhibited the poplar wood´s features. It is worth noting the development of macropores with confined Si3N4 crystals, and particularly in the samples pyrolyzed at 1500 and 1600 °C, one-dimensional Si-based nanostructures, and micro- and mesopores located in cavity walls and within arrangements of the one-dimensional structures, mainly in the materials pyrolyzed at 1400 and 1500 °C. The last materials presented the highest specific surface area values, thus making them potential candidates in catalysts.

Nickel recovery in ferronickel concentrate by green selective reduction of nickel laterite

Nickel laterite is typically processed into ferronickel through a pyrometallurgical method involving high temperatures and the use of fossil fuels, such as coals or cokes. Unfortunately, this process releases emissions like CO2, SO2, and NOx into the environment. This study explores a sustainable approach for nickel laterite processing by investigating low-temperature selective reduction using various biomass reductants. The materials, including saprolitic nickel ore and biomass types (palm kernel shell charcoal or PSC, lamtoro wood charcoal, coconut shell charcoal, and rubber wood charcoal), undergo pelletization, selective reduction at 1150 °C, and wet magnetic separation. PSC biomass is superior to other biomass due to its 217.2 m2/g specific surface area value. Optimal conditions were achieved using 0.3 stoichiometric PSC, along with the addition of 10 wt% of sodium sulfate as an additive. This has led to a nickel mass fraction of 26.0 wt% and a recovery rate of 27.4 %.

Impact of Weak Organic Acids as Coagulants on Tailoring the Properties of Cellulose Aerogel Beads.

Tailoring the properties of cellulose aerogel beads was investigated in the present study by using weak organic acids as coagulants. Three different weak acids were specifically chosen, acetic acid, lactic acid and citric acid. For comparative studies, a strong acid, hydrochloric acid was examined. The production of aerogel beads by conventional dropping technique was controlled and optimized for weak acids. Aerogels were characterized by density analyses, scanning electron microscopy, nitrogen adsorption-desorption analysis, X-ray powder diffractometry and IR spectroscopy. In common, all the aerogel beads showed interconnected nanofibrillar network, high specific surface area, high pore volume, high porosity and meso- and macroporous structure. In particular, when the weakest acid (acetic acid) was used as coagulant in the regeneration bath, the lowest shrinkage was observed. As a result, the cellulose aerogel beads produced from acetic acid showed the highest values of specific surface area (423 m2 g-1) and pore volume (3.6 cm3 g-1). The porous structure can be tuned by the choice of regeneration bath, which has either strong acid or a high concentration of weak acid. The aerogel beads were pure and showed cellulose II crystallinity. Hence this study paves an alternative path way to tailor the properties of cellulose aerogel beads.

Effect of synthesis conditions on the properties of 13X zeolites for CO2 adsorption

ABSTRACT The 13X zeolites were successfully synthesized from sodium silicate and sodium aluminate via hydrothermal treatment, and applied to the adsorption of carbon dioxide (CO2). The properties of the 13X zeolites were characterized and tested by powder X-ray diffraction (XRD), N2-physisorption measurements, CO2-temperature programmed desorption (CO2-TPD) and CO2 adsorption measurements. The results demonstrate that H2O/Na2O, Na2O/SiO2, and SiO2/Al2O3 molar ratios have an important influence on the adsorption performance of CO2 because of their different physicochemical properties. The pure 13X zeolite can be obtained with the optimal H2O/Na2O, Na2O/SiO2 and SiO2/Al2O3 molar ratios of 60, 4 and 3 in the preparation process, respectively. The 13X sample prepared with suitable synthesis conditions possesses the highest crystallinity, the maximum values of specific surface area (720.8 m2/g) and pore volume (0.458 cm3/g) and moderate strength of the interaction between 13X and CO2, thus presenting the highest adsorption capacity of CO2 (118.3 mg/g).

Experimental and theoretical study on the smoldering combustion of size-fractioned forest duff particles

Smoldering combustion process has been suggested as a new method potentially useful in the treatment of biosolids. Natural forest duff (FD) often consists of organic fuel layers with varying particle sizes, yet the influence of the size-fractioned particles on the smoldering combustion dynamics in terms of the heat and mass transfer is not well understood. In this study, the oxidative pyrolysis and smoldering behavior of FD samples with four particle sizes (0 < d1 ≤ 0.425 mm, 0.425 < d2 ≤ 1 mm, 1 < d3 ≤ 2 mm, 2 < d4 ≤ 4 mm) were experimentally and theoretically investigated. Micro-scale thermo-gravimetric (TG) analysis, and a four-step kinetic model incorporating water evaporation, FD pyrolysis, FD oxidation and char oxidation showed that the activation energy of the FD pyrolysis and the ash content are negatively correlated, while the activation energy of the char oxidation increases from 87.26 kJ mol−1 to 119.22 kJ mol−1 with the particle size increasing from d1 to d4. Furthermore, the order of the combustion performance of the FD samples is shown as d1<d2<d4<d3. A series of laboratory-scale smoldering experiments revealed that the peak smoldering temperature increases with the fuel depth while the horizontal spread rate decreases with the fuel depth. Both the peak mass loss rate and the smoldering duration presented a reverse order (d1>d2>d4>d3) of the combustion performance found in the TG tests. A simplified heat transfer analysis qualitatively revealed the beneficial effects of the size-fractioned particles on the smoldering spread rate, while a mass transfer analysis revealed the favorable and adverse influences of the particle size on the kinetic-controlled and diffusion-controlled char oxidation rate, respectively. These findings verify that particle sizes alter the FD physicochemical properties (e.g., specific surface area, bulk density, porosity, permeability, chemical components, and lower calorific value), which in return impact the chemical kinetics, heat and mass transfer process in smoldering combustion. This work provides new insights into the effects of the size-fractioned particles on smoldering combustion, ultimately improving the fundamental understanding for optimizing particle sizes for energy conversion and usage.

Efficient rhodamine B dye photocatalytic degradation in aqueous media using novel ZnO nanomaterials co-doped with Ce and Dy

Water pollution caused by dyes and industrial wastewater poses a significant threat to ecosystems. The purification of such pollutants presents a major challenge. Photocatalysis based on semiconductor materials is a potential wastewater treatment process due to its safety and cost-effectiveness. In the present work, Zn1-2xCexDyxO (x = 0.01–0.05) semiconductors were prepared by the sol-gel auto-ignition method. The samples are denoted CDZO1, CDZO3, and CDZO5 for x = 0.01–0.05, respectively. The X-ray diffraction and Raman spectroscopy results revealed the formation of ZnO hexagonal phase wurtzite structure for all synthesized compositions. Different structural properties were determined. It was found that the lattice parameters and the unit cell volume increased, while the crystallite size diminished as x varied from 0.01 to 0.05. Transmission electron microscopy observations confirmed the formation of nanoparticles with the desired chemical compositions. The specific surface area (SSA) values are found to be 39.95 m2/g, 48.62 m2/g, and 51.36 m2/g for CDZO1, CDZO5, and CDZO5 samples, respectively. The reflectance spectra were recorded to examine the optical properties of the different nanoparticles. The values of the optical band gap were 3.221, 3.225, and 3.239 eV for CDZO1, CDZO3, and CDZO5 samples, respectively. In addition, the photocatalytic performance towards RhB dye degradation for the different samples was assessed. It was established that the CDZO3 sample with a moderate SSA value exhibited the superior photocatalytic performance among the other as-prepared samples wherein the percentage of degradation efficiency, and kinetic constant rate attained their maximum values of 98.22 % and 0.0521 min−1, respectively within 75 min. As per the obtained findings, it is evident that the Zn1-2xCexDyxO photocatalyst has prominent potential for use in the degradation of dyes and offers a useful route for impeding the recombination of electron-hole pairs of zinc oxide material.

Effective Co2+ removal from aqueous solution and industrial wastewater using ZIF-7 and MnFe2O4-modified walnut shell biochar composite

In this study, we developed a novel magnetic composite of walnut shell biochar (WSB) and modified it with ZIF-7 for the purpose of removing Co2+ ions. We conducted a comprehensive evaluation of its performance in Co2+ removal, considering various factors such as contact time, temperature, adsorbent dose, pH, and initial Co2+ concentration. Utilizing response surface methodology-central composite design (RSM-CCD), we examined the interactions between these variables. The specific surface area and magnetic saturation value of the WSB/MnFe2O4/ZIF-7 composite were determined as 170.560 m2.g−1 and 23.469 emu.g−1, respectively. ANOVA analysis indicated that our model effectively captures the interactions between variables, with a high R2 value of 0.9982, explaining 99.82 % of the experimental data. Optimal conditions for maximum Co2+ adsorption efficiency (99.05 %) were identified as follows: a contact time of 44.82 min, pH of 6.04, adsorbent dose of 0.947 mg.L-1, temperature of 25.55 °C, and Co2+ concentration of 11.13 mg.g−1. Kinetic studies revealed that the Pseudo 2nd order kinetic model provided the best fit to the experimental data. The negative entropy parameter indicated a decrease in disorderliness during the adsorption process, while the exothermic nature of adsorption was confirmed by enthalpy values of −92.751 and −40.511 kJ.mol−1 for WSB/MnFe2O4/ZIF-7 and WSB, respectively. Furthermore, the Langmuir isotherm model demonstrated excellent fitting to the isotherm results, suggesting the dominance of homogeneous surfaces in adsorption. The maximum adsorption capacities for Co2+ using WSB/MnFe2O4/ZIF-7 and WSB were determined to be 29.26 and 22.39 mg.g−1, respectively. The WSB/MnFe2O4/ZIF-7 magnetic composite demonstrates promising potential for efficiently removing Co2+ from both natural water sources and industrial wastewater, highlighting its versatility and effectiveness in environmental remediation applications.

Study of the Preparation and Performance of TiO2-Based Magnetic Regenerative Adsorbent.

Against the backdrop of "carbon neutrality", the green treatment of dye wastewater is particularly important. Currently, the adsorption method shows strong application prospects. Therefore, selecting efficient and recyclable adsorbents is of significant importance. TiO2 is an excellent adsorbent, but its difficult recovery often leads to secondary pollution. γ-Fe2O3-modified coal-series kaolin exhibits both excellent adsorption properties and rapid separation through magnetic separation technology. By utilizing the synergistic effects of both, TiO2/-γFe2O3 coal-series kaolin, magnetic adsorbent regeneration materials were prepared using coprecipitation method and characterized. The influencing factors of this functional material on the adsorption of Congo red dye and its regeneration performance are discussed. The experimental results indicated that the specific surface area, pore volume and Ms value of this functional material are 127.5 m2/g, 0.38 cm3/g, and 13.4 emu/g, respectively. It exhibits excellent adsorption characteristics towards Congo red, with an adsorption rate reaching 96.8% within 10 min, conforming to the pseudo-second-order kinetic model, and demonstrating Langmuir IV-type monolayer adsorption. After the adsorption of Congo red, magnetic separation shows superior efficiency. Furthermore, treatment of the adsorbed composite with EDTA allows for recycling, with adsorption rates still above 91% after three cycles, indicating an excellent regeneration capability.

SiOC foam‐aerogel composites: Optimal balance of lightness and excellent thermal insulation

AbstractFoam‐aerogel composites are synthesized in polymeric, hybrid, and ceramic states by completing the open cells of the foam with a solution forming a wet gel, carbon dioxide (CO2) supercritically dried, and pyrolyzed. Thermal diffusivity measurements are conducted using the laser flash, and for mechanical performance, cold crushing tests are done to obtain compressive strengths. Samples possess a range of specific surface area (SSA) values up to ∼650 m2/g contingent upon the material state, that is, polymeric, hybrid, or ceramic. While SSA values can be deliberately altered, almost all samples demonstrated a total porosity of ∼90 vol%, with superb specific compressive strength reaching around 2 MPa. In addition to adjustable surface characteristics granting hydrophobic and hydrophilic features, the study revealed the potential use of these foam‐aerogel composites as thermal insulators with low thermal conductivities of 0.02 W·m−1·K−1 at RT and 0.05 W·m−1·K−1 at 500°C. When exposed directly to a butane flame gun with a flame temperature reaching ∼1200°C, from the backside of a 5 mm‐thick foam‐aerogel composite, only ∼200°C is recorded, which is lower than a comparable commercial insulator panel tested under the same conditions.

Silica extraction from sodium silicate for wollastonite synthesis at low temperatures

In this study, ceramic wollastonite was prepared at low temperatures by using amorphous silica and calcium oxide powders. The amorphous silica was extracted from sodium silicate, while calcium oxide (CaO) was obtained through the calcination of calcium carbonate (CaCO3) particles. The effect of reaction temperature on the formation of wollastonite was systematically investigated. The synthesized powders were analyzed using various characterization techniques, including X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The results indicate that the synthesized silica nanopowders exhibit a notable surface area, with specific surface area (SSA) values reaching 148 m²/g for samples subjected to calcination at 600°C. Furthermore, based on XRD and differential scanning calorimetry (DSC) analyses, it is evident that β-CaSiO3 forms at approximately 780°C and subsequently undergoes complete transformation into α-CaSiO3 at 1200°C. Notably, this study underscores that the utilization of amorphous silica expedites wollastonite formation at lower temperatures compared to those reported in existing literature.

Influence of IDS and SDS compound ratio on pore structure and wettability of bituminous coal and anthracite: Experimental and simulation discussion

The pore and wetting characteristics of bituminous coal and anthracite treated with different proportions of tetrasodium iminodisuccinate (IDS) and sodium dodecyl sulfate (SDS) were measured. The pore structure characteristics of the coal were studied via low-temperature nitrogen adsorption analysis and the Frenkel-Halsey-Hill fractal theory. Zeta potential measurements were conducted to quantitatively analyze the degree of aggregation or dispersion of coal particles dissolved in solution. Changes in the coal surface morphology were observed and analyzed by scanning electron microscopy (SEM). The results show that when the ratio of IDS:SDS is 1:3, the specific surface area (SSA) values of bituminous coal and anthracite are the lowest. The composite reagent has a greater effect on improving the pore structure of anthracite than bituminous coal. Compared with bituminous coal, anthracite has better pore connectivity and a wider pore network. The absolute zeta potentials of bituminous coal and anthracite reach the maximum at an IDS:SDS ratio of 1:3, with values of 91.08 mV and 91.35 mV, respectively. The electrostatic potential distributions of the molecules show that the advantages of the electrostatic potential difference with water molecules enable IDS and SDS molecules to effectively attract water molecules and form hydrogen bonds, thus revealing the optimization mechanism of coal wettability.

HYGROSCOPIC WATER CONTENT AS AN INDICATOR OF SOIL DISPERSITY:THERMODYNAMIC BASIS AND EXPERIMENTAL VERIFICATION

The adsorption properties of dispersed systems are determined by their surface energy, therefore the indicators of hygroscopy (adsorbed water content) and dispersity (specific surface area of the solid phase) of soils and sediments are in close mutual correlation. This well-known empirical fact received a new fundamental interpretation based on the theory of disjoining water pressure according to Deryagin in the form of a thermodynamic equation connecting the specific surface area, hygroscopic water content of soil samples and the relative humidity of the air in the laboratory room. The theoretical equation allowed us to substantiate the methodology for quantifying the hydrophilic specific surface area of soil samples based on widespread data on their hygroscopy. A comparison of the new method with the standard BET-analysis of the specific surface area, as well as with the previously proposed physically based method for its determining by the slope of thermodynamic water retention curves, showed their statistically reliable agreement in a wide range of estimated specific surface area values from 5 to 340 m2×g-1 for soil samples of different genesis and texture.

Reusable adsorbent of magnetite in mesoporous carbon for antibiotic removal.

This study aims to evaluate the feasibility of an innovative reusable adsorbent through adsorption-degradation sequence for antibiotic removal from water. The magnetite/mesoporous carbon adsorbent was prepared using a two-step method of (i) in situ impregnation of magnetite precursor during resorcinol formaldehyde polymerization and (ii) pyrolysis at elevated temperature (800 °C). XRD spectra confirmed that magnetite (Fe3O4) was the only iron oxide species present in the adsorbent, and thermogravimetric analysis revealed that its content was 10 wt%. Nitrogen sorption analysis showed that Fe3O4/carbon features a high fraction of mesopores (> 80 vol.%) and a remarkable specific surface area value (246 m2g-1), outstanding properties for water treatment. The performance of the adsorbent was examined in the uptake of three relevant antibiotics. The maximum adsorption uptakes were ca. 76mgg-1, ca. 70mgg-1, and ca. 44mgg-1 for metronidazole, sulfamethoxazole, and ciprofloxacin, respectively. All adsorption curves were successfully fitted with Langmuir equilibrium model. The regeneration of adsorbent was carried out using Fenton oxidation under ambient conditions. After three consecutive runs of adsorption-regeneration, Fe3O4/carbon maintained its performance almost unchanged (up to 95% of its adsorption capacity), which highlights the high reusability of the adsorbent.

SYNTHESIS OF POLYACRYLAMIDE HYDROGELS WITH PORPHYRIN FRAGMENTS IN THE SIDE CHAIN IN THE PRESENCE OF IMIDAZOLIUM IONIC LIQUIDS

The acrylamide hydrogels containing the porphyrin fragments have been obtained by radical polymerization in a solution. The synthesis has been carried out in the presence of imidazolium ionic liquids with length of the alkyl substituent in the imidazolium ring from C4 to C8. The influence of the used ionic liquids on the structure and some properties of the resulting porphyrin-containing acrylamide hydrogels has been established. The addition of an ionic liquid with a different length of the alkyl substituent into the reaction system can influence the structural changes that occur with the porphyrin comonomer during copolymerization with acrylamide. The formation of bacteriochlorin-like structures is inhibited in the presence of an ionic liquid in the reaction medium. This effect is most noticeable when using an imidazolium ionic liquid with a C8 alkyl substituent length. Hydrogels synthesized in the presence of ionic liquids have lower specific surface area compared to ones obtained without the use of ionic liquids. The lowest specific surface area values were shown by hydrogels synthesized using 1-octyl-3-methylimidazolium bromide. It was also found that the introduction of ionic liquid into the reaction mixture can contribute to both increase and decrease in the numerical values of the sorption characteristics of the resulting hydrogels, depending on the length of the alkyl substituent in the imidazolium ring and a porphyrin : acrylamide ratio. Hydrogels synthesized using 1-hexyl-3-methylimidazolium bromide and 1-octyl-3-methylimidazolium bromide at an initial porphyrin : acrylamide ratio of 1:20 have the highest degree of swelling. Varying the ratio of the initial monomers and the structure of the imidazolium ionic liquid during the copolymerization process allows to control the physicochemical characteristics of the resulting porphyrin-containing hydrogels, which can be useful for solving various applied problems. For citation: Pechnikova N.L., Smirnov A.S., Lyubimtsev A.V., Aleksandriiskiy V.V., Ageeva T.A. Synthesis of polyacrylamide hydrogels with porphyrin fragments in the side chain in the presence of imidazolium ionic liquids. ChemChemTech [Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol.]. 2024. V. 67. N 6. P. 73-79. DOI: 10.6060/ivkkt.20246706.7053.

Biochar from co-pyrolysis of biological sludge and woody waste followed by chemical and thermal activation: end-of-waste procedure for sludge management and biochar sorption efficiency for anionic and cationic dyes

Nine biochars were produced by co-pyrolysis of sawdust and biological sludge following the “design of experiment” approach. Two kinds of sludge (both deriving from the treatment of mixed industrial-municipal wastewater) and two types of woody waste were selected as categorical predicting variables, while contact time, pyrolysis temperature, and sludge percentage were used as quantitative variables. Biochars were analysed for their product characteristics and environmental compatibility based on the European Standards (EN 12915–1:2009) for materials intended for water treatment (i.e. ash content, water leachable polycyclic aromatic hydrocarbons (PAHs) and elements), as well as for specific surface area (SSA), using them as response variables of a multivariate partial least square multiple regression, whose results provided interesting insights on the relationships between pyrolysis conditions and biochar characteristics. Biochars produced with sludge and/or providing the highest SSA values (258–370 m2 g−1) were selected to undergo a sustainable chemical treatment using a by-product of the gasification of woody biomass, complying in all cases with European Standards and achieving therefore the end-of-waste status for sewage sludge. The biochar deriving from the highest percentage of sludge (30% by weight) and with the highest SSA (390 m2 g−1) was thermally activated achieving SSA of 460 m2 g−1 and then tested for the sorption of direct yellow 50 and methylene blue in ultrapure water and real wastewater, compared to a commercial activated carbon (AC). The biochar showed Langmuir sorption maxima (Qm) 2–9 times lower than AC, thus highlighting promising sorption performances. Qm for methylene blue in wastewater (28 mg‧g−1) was confirmed by column breakthrough experiments.