Unveiling the Nature of lignin's Interaction with Molecules: A Mechanistic Understanding of Adsorption of Methylene Blue Dye.

The valorization of lignin into advanced materials for water and soil remediation is experiencing a surge in demand. However, it is imperative that material research and manufacturing be sustainable to prevent exacerbating environmental issues. Meeting these requirements necessitates a deeper understanding of the role of lignin's functional groups in attracting targeted species. This research delves into the interaction mechanisms between lignin and organic molecules, using the adsorption of the cationic dye Methylene Blue (MB+) as a case study. Herein, we aim to quantitatively estimate the contribution of different interaction types to the overall adsorption process. While carbonyl groups were found to have no significant role in attraction, carboxylic groups (-COOH) exhibited significantly lower adsorption compared with hydroxyl groups (-OH). Through alternately blocking aliphatic and phenolic -OH groups, we determined that 61% of the adsorption occurred through hydrogen bonding and 38% via electrostatic interactions. Performance studies of modified lignin along with spectroscopic methods (XPS, FTIR) confirmed the negligible role of π-π interactions in adsorption. This study offers fundamental insights into the mechanistic aspects of MB adsorption on lignin, laying the groundwork for potential modifications to enhance the performance of lignin-based adsorbents. The findings underscore the importance of hydroxyl groups and provide a roadmap for future studies examining the influence of steric factors and interactions with other organic molecules.

Study toward a More Reliable Approach to Elucidate the Lignin Structure-Property-Performance Correlation.

The correlation between lignin structure, its properties, and performance is crucial for lignin engineering in high-value products. Currently, a widespread approach is to compare lignins which differ by more than one parameter (i.e., Kraft vs organosolv vs lignosulfonates) in various applications by attributing the changes in their properties/performance specifically to a certain variable (i.e., phenolic -OH groups). Herein, we suggest a novel approach to overcome this issue by changing only one variable at a time while keeping all others constant before investigating the lignin properties/performance. Indulin AT (Ind-AT), a softwood Kraft lignin, was chosen as the model substrate for this study. Selective (analytical) lignin modifications were used to mask/convert specific functionalities, such as aliphatic (AliphOH) including benzylic -OH (BenzOH) and phenolic -OH (PhOH) groups, carboxyl groups (-COOH) and carbonyl groups (CO) via methylation, acetylation, and reduction. The selectivity and completeness of the reactions were verified by comprehensive NMR analysis (31P and 2D HSQC) of the modified preparations together with state-of-the-art molar mass (MM) characterization. Methylene blue (MB) adsorption, antioxidant activity, and glass transition temperature (Tg) were used to demonstrate and compare the properties/performance of the obtained modified lignins. We found that the contribution of different functionalities in the adsorption of MB follows the trend BenzOH > -COOH > AlipOH > PhOH. Noteworthy, benzylic -OH contributes ca. 3 and 2.3 times more than phenolic and aliphatic -OH, respectively. An 11% and 17% increase of Tg was observed with respect to the unmodified Indulin by methylating benzylic -OH groups and through reduction, respectively, while full acetylation/methylation of aliphatic and phenolic -OH groups resulted in lower Tg. nRSI experiments revealed that phenolic -OH play a crucial role in increasing the antioxidant activity of lignin, while both aliphatic -OH groups and -COOHs possess a detrimental effect, most likely due to H-bonding. Overall, for the first time, we provide here a reliable approach for the engineering of lignin-based products in high value applications by disclosing the role of specific lignin functionalities.

Nucleotide Interaction with a Chitosan Layer on a Silica Surface: Establishing the Mechanism at the Molecular Level.

The growing interest in gene therapy is coupled with the strong need for the development of safe and efficient gene transfection vectors. A composite based on chitosan and fumed silica has been found to be a prospective gene delivery carrier. This study presents an investigation of the nature of the bonds between a series of nucleotides with a chitosan layer deposited on a fumed silica surface. Experimentally measured surface complex formation constants (logK) of the nucleotides were found to be in the range of 2.69-4.02, which is higher than that for the orthophosphate (2.39). Theoretically calculated nucleotide complexation energies for chitosan deposited on the surface range from 11.5 to 23.0 kcal·mol-1, in agreement with experimental data. The adsorption of nucleotides was interpreted using their calculated speciation in an aqueous solution. Based on the structures of all optimized complexes determined from quantum-chemical PM6 calculations, electrostatic interactions between the surface-located NH3+ groups and -PO3H--/-PO32- fragments of the nucleotides were identified to play the decisive role in the adsorption mechanism. The saccharide fragment of monophosphates also plays an important role in the binding of the nucleotides to chitosan through the creation of hydrogen bonds.

Chitosan-Silica Hybrid Composites for Removal of Sulfonated Azo Dyes from Aqueous Solutions.

In this study, the influence of the chitosan immobilization method on the properties of final hybrid materials was performed. Chitosan was immobilized on the surface of mesoporous (ChS2) and fumed silica (ChS3) by physical adsorption and the sol-gel method (ChS1). It was found that physical immobilization of chitosan allows to obtain hybrid composites (ChS) with a homogeneous distribution of polymer on the surface, relatively wide pores, and specific surface area of about 170 m2/g, pHPZC = 5.7 for ChS3 and 356 m2/g and pHPZC = 6.0 for ChS2. The microporous chitosan-silica material with a specific surface area of 600 m2/g and a more negatively charged surface (pHPZC = 4.2) was obtained by the sol-gel reaction. The mechanisms of azo dye adsorption were studied, and the correlation with the composite structure was distinguished. The generalized Langmuir equation and its special cases, that is, Langmuir-Freundlich and Langmuir equations, were applied for the analysis of adsorption isotherm data. The adsorption study showed that physically adsorbed chitosan (ChS1 and ChS2) on a silica surface has a higher sorption capacity, for example, 0.48 mmol/g for the acid red 88 (AR88) dye (ChS2) and 0.23 mmol/g for the acid orange 8 (AO8) dye (ChS1), compared to the composite obtained by the sol-gel method [ChS1, 0.05 mmol/g for the AO8 dye]. For a deeper understanding of the behavior of immobilized chitosan in the adsorption processes, various kinetic equations were applied: first-order, second-order, mixed 1,2-order (MOE), multiexponential, and fractal-like MOE as well as intraparticle and pore diffusion model equations. In the case of AO8 dye, the adsorption rates were differentiated for three composites: for ChS3, 50% of the dye was removed from the solution after merely 5 min and almost 90% after 80 min. The slowest adsorption process controlled by the diffusion rate of dye molecules into the internal space of the pore structure was found for ChS1 (225 min halftime). In the case of ChS2, the rates for various dyes change in the following order: acid orange (AO7) > orange G (OG) > acid red 1 (AR1) > AR88 > AO8 (halftimes: 10.5 < 15.7 < 23.7 < 34.9 < 42.9 min).

Kraft Lignin-Derived Microporous Nitrogen-Doped Carbon Adsorbent for Air and Water Purification.

The study presents a streamlined one-step process for producing highly porous, metal-free, N-doped activated carbon (N-AC) for CO2 capture and herbicide removal from simulated industrially polluted and real environmental systems. N-AC was prepared from kraft lignin─a carbon-rich and abundant byproduct of the pulp industry, using nitric acid as the activator and urea as the N-dopant. The reported carbonization process under a nitrogen atmosphere renders a product with a high yield of 30% even at high temperatures up to 800 °C. N-AC exhibited a substantial high N content (4-5%), the presence of aliphatic and phenolic OH groups, and a notable absence of carboxylic groups, as confirmed by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and Boehm's titration. Porosity analysis indicated that micropores constituted the majority of the pore structure, with 86% of pores having diameters less than 0.6 nm. According to BET adsorption analysis, the developed porous structure of N-AC boasted a substantial specific surface area of 1000 m2 g-1. N-AC proved to be a promising adsorbent for air and water purification. Specifically, N-AC exhibited a strong affinity for CO2, with an adsorption capacity of 1.4 mmol g-1 at 0.15 bar and 20 °C, and it demonstrated the highest selectivity over N2 from the simulated flue gas system (27.3 mmol g-1 for 15:85 v/v CO2/N2 at 20 °C) among all previously reported nitrogen-doped AC materials from kraft lignin. Moreover, N-AC displayed excellent reusability and efficient CO2 release, maintaining an adsorption capacity of 3.1 mmol g-1 (at 1 bar and 25 °C) over 10 consecutive adsorption-desorption cycles, confirming N-AC as a useful material for CO2 storage and utilization. The unique cationic nature of N-AC enhanced the adsorption of herbicides in neutral and weakly basic environments, which is relevant for real waters. It exhibited an impressive adsorption capacity for the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) at 96 ± 6 mg g-1 under pH 6 and 25 °C according to the Langmuir-Freundlich model. Notably, N-AC preserves its high adsorption capacity toward 2,4-D from simulated groundwater and runoff from tomato greenhouse, while performance in real samples from Fyris river in Uppsala, Sweden, causes a decrease of only 4-5%. Owing to the one-step process, high yield, annual abundance of kraft lignin, and use of environmentally friendly activating agents, N-AC has substantial potential for large-scale industrial applications.

Tailoring a bio-based adsorbent for sequestration of late transition and rare earth elements.

The demand for new renewable energy sources, improved energy storage and exhaust-free transportation requires the use of large quantities of rare earth (REE) and late transition (LTM, group 8-12) elements. In order to achieve sustainability in their use, an efficient green recycling technology is required. Here, an approach, a synthetic route and an evaluation of the designed bio-based material are reported. Cotton-derived nano cellulose particles were functionalized with a polyamino ligand, tris(2-aminoethyl) amine (TAEA), achieving ligand content of up to ca. 0.8 mmol g-1. The morphology and structure of the produced adsorbent were revealed by PXRD, SEM-EDS, AFM and FTIR techniques. The adsorption capacity and kinetics of REE and LTM were investigated by conductometric photometric titrations, revealing quick uptake, high adsorption capacity and pronounced selectivity for LTM compared to REE. Molecular insights into the mode of action of the adsorbent were obtained via the investigation of the molecular structure of the Ni(II)-TAEA complex by an X-ray single crystal study. The bio-based adsorbent nanomaterial demonstrated in this work opens up a perspective for tailoring specific adsorbents in the sequestration of REE and LTM for their sustainable recycling.

In Situ Ring-Opening Polymerization of L-lactide on the Surface of Pristine and Aminated Silica: Synthesis and Metal Ions Extraction.

The development of functional materials from food waste sources and minerals is currently of high importance. In the present work, polylactic acid (PLA)/silica composites were prepared by in situ ring-opening polymerizations of L-lactide onto the surface of pristine (Silochrom) and amine-functionalized (Silochrom-NH2) silica. The characteristics of the ring-opening polymerization onto the surface of modified and unmodified silica were identified and discussed. Fourier transform infrared spectroscopy was used to confirm the polymerization of lactide onto the silica surface, and thermogravimetric analysis determined that PLA constituted 5.9% and 7.5% of the composite mass for Silochrom/PLA and Silochrom-NH2/PLA, respectively. The sorption properties of the composites with respect to Pb(II), Co(II), and Cu(II) ions were investigated, and the effect of contact time, initial metal ion concentration, and initial pH were evaluated. Silochrom-NH2/PLA composites were found to have a higher adsorption capacity than Silochrom/PLA for all chosen ions, with the highest adsorption value occurring for Pb2+ at 1.5 mmol/g (90% removal efficiency). The composites showed the highest performance in the neutral or near-neutral pH (created by distilled water or buffer pH 6.86) during the first 15 min of phase contact. The equilibrium characteristics of adsorption were found to follow the Langmuir isotherm model rather than the Freundlich and Temkin models. Perspective applications for these PLA/silicas include remediation of industrial wastewater or leaching solutions from spent lead-acid and Li-ion batteries.

Mesoporous silica adsorbents modified with amino polycarboxylate ligands - functional characteristics, health and environmental effects.

A series of hybrid adsorbents were produced by surface modification with amino polycarboxylate ligands of industrially available microparticles (MP) of Kromasil® mesoporous nanostructured silica beads, bearing grafted amino propyl ligands. Produced materials, bearing covalently bonded functions as EDTA and TTHA, original Kromasil®, bearing amino propyl ligands, and bare particles, obtained by thermal treatment of Kromasil® in air, were characterized by SEM-EDS, AFM, FTIR, TGA and gas sorption techniques. Adsorption kinetics and capacity of surface-modified particles to adsorb Rare Earth Elements (REE), crucial for extraction in recycling processes, were evaluated under dynamic conditions, revealing specificity matching the ligand nature and the size of REE cations. A detailed comparison with earlier reported adsorbents for REE extraction was presented. The cytotoxicity was assessed using four different types of healthy cells, human skeletal muscles derived cells (SKMDC), fibroblast cells, macrophage cells (RAW264.7), and human umbilical vein endothelial cells (HUVECs), indicating lower toxicity of ligand-free MP than MP bearing amino poly-carboxylate functions. Internalization of the MP inside the cells and release of nitric oxide were observed. In addition, zebrafish embryos were exposed to high concentrations of MP and did not show any pronounced toxicity.

Graphitic nitrogen in carbon catalysts is important for the reduction of nitrite as revealed by naturally abundant 15N NMR spectroscopy.

Metal-free nitrogen-doped carbon is considered as a green functional material, but the structural determination of the atomic positions of nitrogen remains challenging. We recently demonstrated that directly-excited solid state 15N NMR (ssNMR) spectroscopy is a powerful tool for the determination of such positions in N-doped carbon at natural 15N isotope abundance. Here we report a green chemistry approach for the synthesis of N-doped carbon using cellulose as a precursor, and a study of the catalytic properties and atomic structures of the related catalyst. N-doped carbon (NH3) was obtained by the oxidation of cellulose with HNO3 followed by ammonolysis at 800 °C. It had a N content of 6.5 wt% and a surface area of 557 m2 g-1, and 15N ssNMR spectroscopy provided evidence for graphitic nitrogen besides regular pyrrolic and pyridinic nitrogen. This structural determination allowed probing the role of graphitic nitrogen in electrocatalytic reactions, such as the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and nitrite reduction reaction. The N-doped carbon catalyst (NH3) showed higher electrocatalytic activities in the OER and HER under alkaline conditions and higher activity for nitrite reduction, as compared with a catalyst prepared by the carbonization of HNO3-treated cellulose in N2. The electrocatalytic selectivity for nitrite reduction of the N-doped carbon catalyst (NH3) was directly related to the graphitic nitrogen functions. Complementary structural analyses by means of 13C and 1H ssNMR, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and low-temperature N2 adsorption were performed and provided support to the findings. The results show that directly-excited 15N ssNMR spectroscopy at natural 15N abundance is generally capable of providing information on N-doped carbon materials if relaxation properties are favorable. It is expected that this approach can be applied to a wide range of solids with an intermediate concentration of N atoms.

LignoPhot: Conversion of hydrolysis lignin into the photoactive hybrid lignin/Bi4O5Br2/BiOBr composite for simultaneous dyes oxidation and Co2+ and Ni2+ recycling.

Valorization of lignin is still an open question and lignin has therefore remained an underutilized biomaterial. This situation is even more pronounced for hydrolysis lignin, which is characterized by a highly condensed and excessively cross-linked structure. We demonstrate the synthesis of photoactive lignin/Bi4O5Br2/BiOBr bio-inorganic composites consisting of a lignin substrate that is coated by semiconducting nanosheets. The XPS analysis reveals that growing these nanosheets on lignin instead on cellulose prevents the formation of Bi5+ ions at the surface region, yielding thus a modified heterojunction Bi4O5Br2/BiOBr. The material contains 18.9% of Bi4O5Br2/BiOBr and is effective for the photocatalytic degradation of cationic methylene blue (MB) and zwitterionic rhodamine B (RhB) dyes under light irradiation. Lignin/Bi4O5Br2/BiOBr decreases the dye concentration from 80 mg L-1 to 12.3 mg L-1 for RhB (85%) and from 80 mg L-1 to 4.4 mg L-1 for MB (95%). Complementary to the dye degradation, the lignin as a main component of the composite, was found to be efficient and rapid biosorbent for nickel, lead, and cobalt ions. The low cost, stability and ability to simultaneously photo-oxidize organic dyes and adsorb metal ions, make the photoactive lignin/Bi4O5Br2/BiOBr composite a prospective material for textile wastewaters remediation and metal ions recycling.

Lignin-Inorganic Interfaces: Chemistry and Applications from Adsorbents to Catalysts and Energy Storage Materials.

Lignin is one the most fascinating natural polymers due to its complex aromatic-aliphatic structure. Phenolic hydroxyl and carboxyl groups along with other functional groups provide technical lignins with reactivity and amphiphilic character. Many different lignins have been used as functional agents to facilitate the synthesis and stabilization of inorganic materials. Herein, the use of lignin in the synthesis and chemistry of inorganic materials in selected applications with relevance to sustainable energy and environmental fields is reviewed. In essence, the combination of lignin and inorganic materials creates an interface between soft and hard materials. In many cases it is either this interface or the external lignin surface that provides functionality to the hybrid and composite materials. This Minireview closes with an overview on future directions for this research field that bridges inorganic and lignin materials for a more sustainable future.

Chitosan Deposited onto Fumed Silica Surface as Sustainable Hybrid Biosorbent for Acid Orange 8 Dye Capture: Effect of Temperature in Adsorption Equilibrium and Kinetics.

Chitosan was deposited on fumed silica without the addition of cross-linkers or activating agents. The chitosan surface layer has a high affinity toward organic molecules, e.g., Acid Orange 8 (AO8) dye, robust to a broad range of simulated conditions (variance with respect to temperature, time, and concentration of solute). Experimental equilibrium data were analyzed by the generalized Langmuir equation taking into consideration the energetic heterogeneity of the adsorption system. The effect of temperature on dye uptake and adsorption rate was studied. According to the calculated thermodynamic functions ΔG°, ΔH°, and ΔS° from the equilibrium data at different temperatures, the adsorption of AO8 onto chitosan-fumed silica composite is exothermic and spontaneous. The studies of temperature effect on adsorption equilibrium show that the maximum adsorption capacity (determined from the Langmuir-Freundlich equation) of synthesized composite toward AO8 is about one-third higher in the case of an isotherm measured at 5 °C than this value obtained for the isotherm measured at 45 °C. The quantitative binding of dye molecules to chitosan coating on the surface of silica was proved by 1H MAS NMR. The deep kinetics study through the application of various theoretical models-the first-order equation, pseudo-first-order equation, second-order equation, pseudo-second-order equation, mixed first, second-order equation, and multiexponential equation-was applied for getting inside the mechanism of AO8 binding to the chitosan coating. Structural characteristics of chitosan-coated silica were obtained from the low-temperature adsorption/desorption isotherms of nitrogen and imaging by scanning electron microscopy. The effects of a synthetic route for polymer coating on thermal stability and the ability to degrade were studied by differential scanning calorimetry.

NiO/Poly(4-alkylthiazole) Hybrid Interface for Promoting Spatial Charge Separation in Photoelectrochemical Water Reduction.

Conjugated polymers are emerging as alternatives to inorganic semiconductors for the photoelectrochemical water splitting. Herein, semi-transparent poly(4-alkylthiazole) layers with different trialkylsilyloxymethyl (R3SiOCH2-) side chains (PTzTNB, R = n-butyl; PTzTHX, R = n-hexyl) are applied to functionalize NiO thin films to build hybrid photocathodes. The hybrid interface allows for the effective spatial separation of the photoexcited carriers. Specifically, the PTzTHX-deposited composite photocathode increases the photocurrent density 6- and 2-fold at 0 V versus the reversible hydrogen electrode in comparison to the pristine NiO and PTzTHX photocathodes, respectively. This is also reflected in the substantial anodic shift of onset potential under simulated Air Mass 1.5 Global illumination, owing to the prolonged lifetime, augmented density, and alleviated recombination of photogenerated electrons. Additionally, coupling the inorganic and organic components also enhances the photoabsorption and amends the stability of the photocathode-driven system. This work demonstrates the feasibility of poly(4-alkylthiazole)s as an effective alternative to known inorganic semiconductor materials. We highlight the interface alignment for polymer-based photoelectrodes.

Membrane-Filtered Kraft Lignin-Silica Hybrids as Bio-Based Sorbents for Cobalt(II) Ion Recycling.

Efficient and sustainable recycling of cobalt(II) is of increasing importance to support technological development in energy storage and electric vehicle industries. A composite material based on membrane-filtered lignin deposited on nanoporous silica microparticles was found to be an effective and sustainable sorbent for cobalt(II) removal. This bio-based sorbent exhibited a high sorption capacity, fast kinetics toward cobalt(II) adsorption, and good reusability. The adsorption capacity was 18 mg Co(II) per gram of dry adsorbent at room temperature (22 °C) at near-neutral pH, three times higher than that of the summarized capacity of lignin or silica starting materials. The kinetics study showed that 90 min is sufficient for effective cobalt(II) extraction by the composite sorbent. The pseudo-second-order kinetics and Freundlich isotherm models fitted well with experimentally obtained data and confirmed heterogeneity of adsorption sites. The promising potential of the lignin-silica composites for industrial applications in the cobalt recovering process was confirmed by high values of desorption in mildly acidic solutions.

Nanostructured core-shell metal borides-oxides as highly efficient electrocatalysts for photoelectrochemical water oxidation.

Oxygen evolution reaction (OER) catalysts are critical components of photoanodes for photoelectrochemical (PEC) water oxidation. Herein, nanostructured metal boride MB (M = Co, Fe) electrocatalysts, which have been synthesized by a Sn/SnCl2 redox assisted solid-state method, were integrated with WO3 thin films to build heterojunction photoanodes. As-obtained MB modified WO3 photoanodes exhibit enhanced charge carrier transport, amended separation of photogenerated electrons and holes, prolonged hole lifetime and increased charge carrier density. Surface modification of CoB and FeB significantly enhances the photocurrent density of WO3 photoanodes from 0.53 to 0.83 and 0.85 mA cm-2, respectively, in transient chronoamperometry (CA) at 1.23 V vs. RHE (VRHE) under interrupted illumination in 0.1 M Na2SO4 electrolyte (pH 7), corresponding to an increase of 1.6 relative to pristine WO3. In contrast, the pristine MB thin film electrodes do not produce noticeable photocurrent during water oxidation. The metal boride catalysts transform in situ to a core-shell structure with a metal boride core and a metal oxide (MO, M = Co, Fe) surface layer. When coupled to WO3 thin films, the CoB@CoOx nanostructures exhibit a higher catalytic enhancement than corresponding pure cobalt borate (Co-Bi) and cobalt hydroxide (Co(OH)x) electrocatalysts. Our results emphasize the role of the semiconductor-electrocatalyst interface for photoelectrodes and their high dependency on materials combination.

Electrostatic Deposition of the Oxidized Kraft Lignin onto the Surface of Aminosilicas: Thermal and Structural Characteristics of Hybrid Materials.

In recent years, functional polymeric compounds have been widely used to modify the silica surface, which allows one to obtain the corresponding organomineral composites for broad application prospects. In this case, lignin-a cross-linked polyphenolic macromolecule-is of great interest according to its valuable properties and possible surplus as a by-product of pulp and paper industry and various biorefinery processes. Hybrid materials based on kraft softwood lignin and silica were obtained via the electrostatic attraction of oxidized lignin to the aminosilica surface with different porosities, which were prepared by the amination of the commercial silica gel with an average pore diameter of 6 nm, and the silica prepared in the lab with the oxidized kraft lignin and lignin-silica samples with an average pore diameter of 38 nm was investigated by physicochemical methods: two-dimensional nuclear magnetic resonance (NMR), 31P NMR, Fourier transform infrared spectroscopy, thermogravimetric analysis in nitrogen and air atmosphere, scanning electron microscopy, and adsorption methods. After oxidation, the content of carboxylic groups almost doubled in the oxidized lignin, compared to that in the native one (0.74 mmol/g against 0.44 mmol/g, respectively). The lignin content was deposited onto the surface of aminosilica, depending on the porosity of the silica material and on the content of amino groups on its surface, giving lignin-aminosilica with 20% higher lignin content than the lignin-aminosilica gel. Both types of lignin-silica composites demonstrate a high sorptive capacity toward crystal violet dye. The suggested approach is an easy and low-cost way of synthesis of lignin-silica composites with unique properties. Such composites have a great potential for use as adsorbents in wastewater treatment processes.

Peculiarities of Synthesis and Properties of Lignin⁻Silica Nanocomposites Prepared by Sol-Gel Method.

The development of advanced hybrid materials based on polymers from biorenewable sources and mineral nanoparticles is currently of high importance. In this paper, we applied softwood kraft lignins for the synthesis of lignin/SiO2 nanostructured composites. We described the peculiarities of composites formation in the sol-gel process through the incorporation of the lignin into a silica network during the hydrolysis of tetraethoxysilane (TEOS). The initial activation of lignins was achieved by means of a Mannich reaction with 3-aminopropyltriethoxysilane (APTES). In the study, we present a detailed investigation of the physicochemical characteristics of initial kraft lignins and modified lignins on each step of the synthesis. Thus, 2D-NMR, 31P-NMR, size-exclusion chromatography (SEC) and dynamic light scattering (DLS) were applied to analyze the characteristics of pristine lignins and lignins in dioxan:water solutions. X-Ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) were used to confirm the formation of the lignin⁻silica network and characterize the surface and bulk structures of the obtained hybrids. Termogravimetric analysis (TGA) in nitrogen and air atmosphere were applied to a detailed investigation of the thermal properties of pristine lignins and lignins on each step of modification. SEM confirmed the nanostructure of the obtained composites. As was demonstrated, the activation of lignin is crucial for the sol-gel formation of a silica network in order to create novel hybrid materials from lignins and alkoxysilanes (e.g., TEOS). It was concluded that the structure of the lignin had an impact on its reactivity during the activation reaction, and consequently affected the properties of the final hybrid materials.

Imidazole-2yl-Phosphonic Acid Derivative Grafted onto Mesoporous Silica Surface as a Novel Highly Effective Sorbent for Uranium(VI) Ion Extraction.

A new imidazol-2yl-phosphonic acid/mesoporous silica sorbent (ImP(O)(OH)2/SiO2) was developed and applied for uranium(VI) ion removal from aqueous solutions. The synthesized material was characterized by fast kinetics and an extra-high adsorption capacity with respect to uranium. The highest adsorption efficiency of U(VI) ions was obtained for the reaction system at pH 4 and exceeded 618 mg/g. The uranium(VI) sorption proceeds quickly in the first step within 60 min of the adsorbent sites and ion interactions. Moreover, the equilibrium time was determined to be 120 min. The equilibrium and kinetic characteristics of the uranium(VI) ions uptake by synthesized sorbent was found to follow the Langmuir-Freundlich isotherm model and pseudo-second-order kinetics rather than the Langmuir, Dubinin-Radushkevich, and Temkin models and pseudo-first-order or intraparticle diffusion sorption kinetics. The adsorption mechanism for uranium on the sorbent was clarified basing on the X-ray photoelectron spectroscopy (XPS) analysis. The model of UO22+ binding to surface of the sorbent was proposed according to the results of XPS, i.e., a 1:1 U-to-P ratio in the sorbed complex was established. The regeneration study confirms the ImP(O)(OH)2/SiO2 sorbent can be reused. A total of 45% of uranium ions was determined as originating from the sorbent leaching in the acidic solutions, whereas when the basic solutions were used, the removal efficiency was 12%.

Silica with immobilized phosphinic acid-derivative for uranium extraction.

A novel adsorbent benzoimidazol-2-yl-phenylphosphinic acid/aminosilica adsorbent (BImPhP(O)(OH)/SiO2NH2) was prepared by carbonyldiimidazole-mediated coupling of aminosilica with 1-carboxymethylbenzoimidazol-2-yl-phenylphosphinic acid. It was obtained through direct phosphorylation of 1-cyanomethylbenzoimidazole by phenylphosphonic dichloride followed by basic hydrolysis of the nitrile. The obtained sorbent was well characterized by physicochemical methods, such as differential scanning calorimetry-mass spectrometry (DSC-MS), surface area and pore distribution analysis (ASAP), scanning electron microscopy (SEM), X-ray photoelectron (XPS) and Fourier transform infrared (FTIR) spectroscopies. The adsorption behavior of the sorbent and initial silica gel as well as aminosilica gel with respect to uranium(VI) from the aqueous media has been studied under varying operating conditions of pH, concentration of uranium(VI), contact time, and desorption in different media. The synthesized material was found to show an increase in adsorption activity with respect to uranyl ions in comparison with the initial compounds. In particular, the highest adsorption capacity for the obtained modified silica was found at the neutral pH, where one gram of the adsorbent can extract 176mg of uranium. Under the same conditions the aminosilica extracts 166mg/g, and the silica - 144mg/g of uranium. In the acidic medium, which is common for uranium nuclear wastes, the synthesized adsorbent extracts 27mg/g, the aminosilica - 16mg/g, and the silica - 14mg/g of uranium. It was found that 15% of uranium ions leached from the prepared material in acidic solutions, while 4% of uranium can be removed in a phosphate solution.

Synthesis and adsorption properties of chitosan-silica nanocomposite prepared by sol-gel method.

A hybrid nanocomposite material has been obtained by in situ formation of an inorganic network in the presence of a preformed organic polymer. Chitosan biopolymer and tetraethoxysilane (TEOS), which is the most common silica precursor, were used for the sol-gel reaction. The obtained composite chitosan-silica material has been characterized by physicochemical methods such as differential thermal analyses (DTA); carbon, hydrogen, and nitrogen (CHN) elemental analysis; nitrogen adsorption/desorption isotherms, scanning electron microscopy (SEM); and Fourier transform infrared (FTIR) spectroscopy to determine possible interactions between silica and chitosan macromolecules. Adsorption of microquantities of V(V), Mo(VI), and Cr(VI) oxoanions from the aqueous solutions by the obtained composite has been studied in comparison with the chitosan beads, previously crosslinked with glutaraldehyde. The adsorption capacity and kinetic sorption characteristics of the composite material were estimated.