Selective Removal Research Articles

All‐in‐One: Photo‐Responsive Lanthanide‐Organic Framework for Simultaneous Sensing, Adsorption, and Photocatalytic Reduction of Uranium

AbstractThe selective removal and immobilization of uranyl ions from aqueous solutions is essential for the sustainable development of nuclear energy. Herein, a robust lanthanide‐organic framework material (IHEP‐24) is developed for simultaneous fluorescence sensing, selective adsorption, and photocatalytic reduction of uranium, integrating three different functions in one material. The confined space formed by the coordination assembly of viologen derivative ligands and metal‐oxygen clusters can act as precise recognition sites for uranyl, allowing IHEP‐24 to efficiently detect and capture uranyl ions. In addition, the presence of a viologen‐based radical ligand enables IHEP‐24 to a further photocatalytic reduction of the adsorbed uranyl to amorphous UO2. The mechanisms of adsorption and photocatalysis are revealed by batch experiments, photoelectrochemical characterizations, and theoretical calculations. This study provides a reference for the construction of robust multi‐functional MOF materials and also provides support for the deep removal and immobilization of radionuclides from aqueous solution.

Achievements in Preparation of Cyclodextrin–Based Porous Materials for Removal of Pollutants

Cyclodextrin–based porous materials have been widely applied in removing various organic pollutants from water environments, due to their unique physical and chemical properties, like the size–matching effect and hydrophobic interaction. Large numbers of hydroxyl groups in its external structure give cyclodextrin a high solubility in water, but the existence of these hydroxyl groups also endows cyclodextrin with the ability to be chemically modified with various functional groups to reduce its solubility in water and, meanwhile, to develop some novel functionalized cyclodextrin–based porous materials for selective removal of the target organic pollutants. This review focuses on the recent development in the synthesis of cyclodextrin–based porous materials (crosslinked cyclodextrin polymers and immobilized cyclodextrins), as well as highlighting their applications and mechanisms in the removal of dyes, endocrine disruptors, and mixed pollutants from water. Finally, the challenges and future perspectives in related research fields are discussed.

Enhanced Hydrogen Evolution in Porous and Hybrid g‐C3N4/Pt‐PVDF Electrospun Membranes via Piezoelectricity from Water Flow Energy

AbstractInspired from seaweed swayed by waves, the enhanced hydrogen evolution is realized in porous and hybrid g‐C3N4/Pt‐PVDF electrospun membranes via piezoelectricity from water flow energy. The membranes are fabricated by dispersing g‐C3N4/Pt into the mixed solution of PVDF and PEO, followed by electrospinning and selective removal of PEO. By changing the PEO amount, the pore size in nanofibers is adjusted. Due to the hydrogen bonding between g‐C3N4/Pt and PVDF, the β phase of PVDF is increased, beneficial for the piezoelectricity performance. When the electrospun membranes are exposed to water flow, an additional potential field is triggered due to the deformation of PVDF. It not only eases the photogeneration of charge carriers from g‐C3N4/Pt but also hinders their recombination. The prolonged lifetime significantly improves the photocatalytic water splitting of g‐C3N4/Pt under visible light. The hydrogen evolution in the electrospun membranes (PVDF to PEO = 4:1) is profoundly improved to 9 278 µmol h−1 g−1, almost doubled to the pure g‐C3N4/Pt nanosheets (5 220 µmol h−1 g−1). Therefore, the seaweed‐inspired electrospun membrane is a promising strategy for the efficiently photocatalytic water splitting via g‐C3N4 in an aqueous environment, such as a natural sea and lake, by the piezoelectricity gained from the water flow energy.

Breaking hydrogen bond in metal free carbon nitride to induce peroxymonosulfate nonradical activation: Surface-mediated electron transfer

Breaking hydrogen bond in metal free carbon nitride (CN) to increase peroxymonosulfate (PMS) adsorption for surface-mediated electron transfer has been challenging. Herein, we incorporated N−CN monomer into CN to break hydrogen bond by the introduction of polyvinylpyrrolidone (PVP). The developed nonradical oxidation system achieved selective decomposition of highly hydrophilic contaminants and efficient removal of chemical oxygen demand (58.0%), total phosphorus (88.1%), ammonia nitrogen (100.0%) and total nitrogen (67.8%) from the secondary effluent in a continuous flow reactor. This was attributed to that the breakage of hydrogen bond accelerated the redistribution of electron densities at C and N sites, leading to an increase in the adsorption energy of N site to PMS. This promoted the formation of PVP/CN-PMS* complex for the selective and efficient removal of organics and inorganics. This work provided a new perspective for the selective and long-term treatment of practical wastewater.

Harnessing the power of multifunctional γ-Fe2O3@CuO nanocomposites: Effective extraction of heavy metals and bacterial pathogens from contaminated water

Waterborne diseases and carcinogenic effects associated with heavy metal poisoning have drawn considerable attentionto removing heavy metals from contaminated water and killing disease-causing bacteria. In this regard, γ-Fe2O3 nanoparticles (NPs) were synthesized by ion reduction method, while CuO NPsand γ-Fe2O3–CuO nanocomposites (NCs) by hydrothermal method. XRD, FTIR, FESEM, EDX and UV–visible spectroscopy were used for system characterization. The dumbbell shape of CuO NPs and spherical shape of γ-Fe2O3 NPs and γ-Fe2O3@CuO NCs were indicated via SEM analysis. The elemental composition and successful synthesis of γ-Fe2O3@CuONCs were confirmed by EDX results. The order for elemental composition: O > Cu > Fe showed the higher content ratio of Cu and O while Fe has the lowest content. The antibacterial activities against E. Coli and B. subtili were evaluated by Minimum Inhibitory Concentration (MIC) and Zone of Inhibition. γ-Fe2O3@CuO NCs showed excellent antibacterial performance as compared to γ-Fe2O3 NPs,CuO NPs, commercial Cu NPs and Cu salt. The drastic improvement in properties of γ-Fe2O3@CuO NCs resulted in better surface contact and extensive cell membranes rupture to eliminate bacterial pathogens present in wastewater Batch adsorption experiments were performed for selective removal of toxic Pb2+ ionsexisting in polluted water. The greatest adsorption capacity was determined to be 346 mg/g, and the highest removal percentage of 95 % was achieved at pH 4 in 60 min. Isotherm models and kinetic studies indicated that Pb2+ ions followed pseudo-second-order kinetics. The results obtained from batch adsorption experiment revealed γ-Fe2O3@CuO NCs as effective nanosorbent for quick elimination of toxic metal ions from industrial wastewater.

Selective removal of chromium from laterite residue with high content of iron by the co-operation of phosphoric acid and oxalic acid

With the rising demand for nickel and cobalt, laterite residue containing chromium is extensively generated through the laterite hydrometallurgical process, posing a significant burden on environmental protection and the sustainable development of the nickel industry. This study presents a novel and environmentally friendly method for selectively extracting chromium from laterite residue and yielding iron phosphate concentrate. In this method, iron, as the major component, is simultaneously transformed into iron phosphate as solid state, while chromium is extracted into solution by a minimal amount of phosphoric acid. The effects of phosphoric acid and oxalic acid usage, temperature, liquid-to-solid ratio, and leaching time on the transformation and removal were investigated. Thermodynamic analysis and experimental results indicated that the addition of oxalic acid promoted chromium extraction with minimal impact on the transformation of hematite and iron phosphate. The results of SEM, XPS, and XRD revealed the conversion of laterite residue to iron phosphate. At an oxalic acid dosage of 10 %, almost 90 % of the iron remained in the residue as iron phosphate, while over 60 % of the chromium was extracted into the solution, resulting in a chromium concentration of 1.1 g/L. The solution underwent a two-step treatment process, primarily to recycle the soluble iron species. The extracted chromium was captured by adding calcium hydroxide at pH ∼ 3.0 in the form of phosphate.

Narrow spectrum nano-antibiotic for selective removal of ARB from contaminated water: New insights into stimuli response based on cellular attachment, lysis, and excretion

Narrow spectrum nano-antibiotics are supposedly the future trouble-shooters to improve the efficacy of conventional antimicrobials for treatment of severe bacterial infections, remove contamination from water and diminish the development of antibiotic resistance. In this study, antimicrobial peptide functionalized boron-carbon-nitride nanosheets ((Ant)pep@BCN NSs) are developed that are a promising wastewater disinfector and antibiotic resistant bactericide agent. These nanosheets are developed for selective removal and effective inactivation of antibiotic resistant bacteria (ARB) from water in presence of two virulent bacteria. The (Ant)pep@BCN NSs provide reactive surface receptors specific to the ARB. They mimic muralytic enzymes to damage the cell membrane of ARB. These NSs demonstrate 3-fold higher antimicrobial efficiency against the targeted ARB compared to pristine BCN even at lower concentrations. To the best of our knowledge, this is the first time that functionalized BCN has been developed to remove ARB selectively from wastewater. Furthermore, the (Ant)pep@BCN selectively reduced the microbiological load and led to morphological changes in Gram negative ARB in a mixed bacterial inoculum. These ARBs excreted outer–inner membrane vesicles (OIMVs) of triangular shape as a stimuli response to (Ant)pep@BCN NSs. These novel antimicrobial peptide-NSs have potential to improve treatment efficacy against ARB infections and water contamination.

Insight into the Mechanisms of Efficient Selective Removal of Pb2+ from Wastewater by Nano-flowered MoS2/NHCS Electrodes

The shortage of clean water resources has become a major challenge to global sustainable development, and lead (Pb) pollution in natural water has made the issue even more severe. Efficiently removal of Pb2+ is a severe challenge to Lead-containing sewage disposal. Here, efficiently selective removal of Pb2+ from wastewater was tested over hollow nano-flowered MoS2/N-doped hollow carbon spheres (MoS2/NHCS) cathodes by capacitive deionization (CDI) process. The MoS2/NHCS electrodes exhibited an excellent removal efficiency of 96.9% in 20 ppm Pb(NO3)2 solution at U = 1.2V, pH = 6, and 40mL/min of flow rate. In addition, MoS2/NHCS electrodes showed excellent regeneration ability in 10 ppm Pb2+ solution and still could reach 97.7% after 20 cycles, especially the good selective removal efficiency in the mixed solution. In situ Raman spectrum and DFT calculations indicate that efficient selective removal of Pb2+ was attributed to Pb2+ directly combined with partially negatively charged S2- to generate PbS, and some S ions transformed into S2-2 by received electrons, which further combines with Pb2+ to form PbS2. Hence, this work proposes an innovative adsorption mechanism for selective capacitive removal of Pb2+ and provides the potential practical application for treating Lead-containing wastewater.

One-pot extraction of nanocellulose from raw durian husk fiber using carboxylic acid-based deep eutectic solvent with in situ ultrasound assistance

Nanocellulose (CNF) has emerged as a promising alternative to synthetic petroleum-based polymers, but the conventional preparation process involves multiple tedious steps, heavily dependent on chemical input, and proves cost-inefficient. This study presented an, in situ ultrasound-assisted extraction using deep eutectic solvent (DES) based on choline chloride and oxalic acid for more facile production of CNF from raw durian husk fibers. FESEM analysis confirmed the successful extraction of web-like nanofibril structure with width size ranging from 18 to 26 nm. Chemical composition analysis and FTIR revealed the selective removal of lignin and hemicellulose from the raw fiber. As compared to post-ultrasound treatment, in situ ultrasound-assisted extraction consistently outperforms, yielding a higher CNF yield with finer fiber width and significantly reduced lignin content. Integrating this eco-friendly in situ ultrasonication-assisted one-pot extraction method with a 7.5 min interval yielded the highest CNF yield of 58.22 % with minimal lignin content. The superior delignification ability achieved through the proposed in situ ultrasound-assisted protocol surpasses the individual efficacy of DES and ultrasonication processes, neither of which yielded CNF in our experimental setup. This single-step fabrication process significantly reduces chemical usage and streamlines the production steps yielding web-structured CNF that is ideal for sustainable application in membrane and separator.

Bacitracin Methylene Disalicylate (BMD) Treatment Affects Spleen Proteome in Broiler Chicks Infected with Salmonella enteritidis

Bacitracin Methylene Disalicylate (BMD), as a feed additive to poultry diets, enhances digestion, prevents Salmonella enteritidis (SE) colonization, and treats current infections. The objective of this study was to utilize a quantitative proteomic approach to determine the effect of BMD feed additive on broiler chickens challenged with SE in the spleen proteome. At 1 d of age, chicks were randomly allocated into four groups: control with and without SE challenge (CON, n = 60; CON-SE, n = 60), BMD with and without SE challenge (BMD, n = 60; BMD-SE, n = 60). Birds in the CON-SE and BMD-SE treatment were administered SE inoculum by oral gavage. On day three and day seven post-gavage, the spleen was collected aseptically from birds in each treatment group (CON, n = 4/day; CON-SE, n = 4/day; BMD, n = 4/day; BMD-SE, n = 4/day). Proteomic analysis by liquid chromatography-tandem mass spectrometry (LC-MS/MS) showed an increased abundance of 115 proteins and decreased of 77 due to the BMD. Proteins that decreased in abundance were enriched for fibrinogen complex and extracellular space, whereas proteins that increased in abundance were enriched for proteasome-mediated ubiquitin-dependent protein catabolic process and mitochondrion. Analysis of the interaction between BMD and the Salmonella challenge found 230 differentially abundant proteins including proteins associated with RNA binding, spliceosome, protein transport, and cell adhesion among the upregulated proteins, and those associated with protein folding, carbon metabolism, biosynthesis of nucleotide sugars, response to oxidative stress, positive regulation of NIK/NF-kappaB signaling, and inflammatory response among the downregulated proteins. The impact of BMD treatment on spleen proteome indicates an anti-apoptotic effect. BMD also modified the response of the spleen to the SE challenge with a marked decrease in proteins that prompt cytokine synthesis and an increase in proteins involved in the selective removal of unfolded proteins.

Surface nanostructuring of Ti40Cu40Zr11Fe3Sn3Ag3 amorphous alloy by alkaline chemical treatment for potential use as a biocompatible material

Amorphous alloys show potential as implant materials due to their superior mechanical properties and good corrosion resistance. However, the presence of toxic elements in the alloy composition can pose challenges, as they can react with the surrounding tissue, leading to inflammation and cell death. To address this, Ti40Cu40Zr11Fe3Sn3Ag3 at% amorphous alloy is developed. This composition comprises of biocompatible elements (Ti, Zr, and Sn) and antimicrobial elements (Ag, Fe, and Cu), for potential use as implant materials. Chemical pseudo-dealloying using a solution of ammonium hydroxide and hydrogen peroxide is employed to selectively remove copper from the sample surface, which may induce toxicity by prolonged contact, and promote the formation of a patterned passivating Ti/Zr oxide-rich surface to enable possible antimicrobial effects. The surface of the samples was analyzed using atomic force microscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy. The modified surfaces show titanium oxide-rich nanostructured topography with depleted amounts of copper from the surface. The kinetics of the selective removal of copper, and the influence of parameters such as electrolyte concentration, immersion time, and stirring velocity on the evolution of morphology were investigated. Our findings elucidate the mechanism of pseudo-dealloying using an ammonia-based solution and demonstrate its efficacy in enhancing the biocompatibility of the alloy. In detail, the pseudo-dealloyed samples exhibited hydrophilic interactions and demonstrated hemocompatibility, making them promising candidates for blood-contacting medical devices. This study underscores the significance of our approach in tailoring the surface properties of amorphous alloys for biomedical applications, paving the way for their utilization in implant materials with improved biocompatibility.

Simultaneous Rosiglitazone Release and Low-Density Lipoprotein Removal by Chondroitin Sodium Sulfate/Cyclodextrin/Poly(acrylic acid) Composite Adsorbents for Atherosclerosis Therapy.

Atherosclerosis (AS) is characterized by the accumulation of substantial low-density lipoprotein (LDL) and inflammatory response. Hemoperfusion is commonly employed for the selective removal of LDL from the body. However, conventional hemoperfusion merely focuses on LDL removal and does not address the symptom of plaque associated with AS. Based on the LDL binding properties of acrylated chondroitin sodium sulfate (CSA), acrylated beta-cyclodextrin (CD) and acrylic acid (AA), along with the anti-inflammatory property of rosiglitazone (R), the fabricated AA-CSA-CD-R microspheres could simultaneously release R and facilitate LDL removal for hemoperfusion. The AA and CSA offer electrostatic adsorption sites for LDL, while the CD provides hydrophobic adsorption sites for LDL and weak binding sites for R. According to the Sips model, the maximum static LDL adsorption capacity of AA-CSA-CD-R is determined to be 614.73 mg/g. In dynamic simulated perfusion experiments, AA-CSA-CD-R exhibits an initial cycle LDL adsorption capacity of 150.97 mg/g. The study suggests that the weakened inflammatory response favors plaque stabilization. The anti-inflammatory property of the microspheres is verified through an inflammation model, wherein the microsphere extracts are cocultured with mouse macrophages. Both qualitative analysis of iNOS\TNF-α and quantitative analysis of IL-6\TNF-α collectively demonstrate the remarkable anti-inflammatory effect of the microspheres. Therefore, the current study presents a novel blood purification treatment of eliminating pathogenic factors and introducing therapeutic factors to stabilize AS plaque.

Selective Removal of Hemicellulose by Diluted Sulfuric Acid Assisted by Aluminum Sulfate.

Hemicellulose can be selectively removed by acid pretreatment. In this study, selective removal of hemicellulose was achieved using dilute sulfuric acid assisted by aluminum sulfate pretreatment. The optimal pretreatment conditions were 160 °C, 1.5 wt% aluminum sulfate, 0.7 wt% dilute sulfuric acid, and 40 min. A component analysis showed that the removal rate of hemicellulose and lignin reached 98.05% and 9.01%, respectively, which indicated that hemicellulose was removed with high selectivity by dilute sulfuric acid assisted by aluminum sulfate pretreatment. Structural characterizations (SEM, FTIR, BET, TGA, and XRD) showed that pretreatment changed the roughness, crystallinity, pore size, and functional groups of corn straw, which was beneficial to improve the efficiency of enzymatic hydrolysis. This study provides a new approach for the high-selectivity separation of hemicellulose, thereby offering novel insights for its subsequent high-value utilization.

Smart Pillar[5]arene‐Based PDMAEMA/PES Beads for Selective Dye Pollutants Removal: Design, Synthesis, Chemical‐Physical Characterization, and Adsorption Kinetic Studies

Smart Pillar[5]arene‐Based PDMAEMA/PES Beads for Selective Dye Pollutants Removal: Design, Synthesis, Chemical‐Physical Characterization, and Adsorption Kinetic Studies

Multiparameter signal-to-noise ratio optimization for end milling cutting conditions of aluminium alloy 5083

AbstractSurface integrity problems during selective material removal processes are a very common limitation for process productivity and part quality, especially in difficult-to-machine materials like 5083 aluminium alloy (AA), which is known for its remarkable performance in extreme environments. In general, tuning the cutting-part material properties with cutter geometry and cutting parameters can optimize surface texture, increase parts accuracy and resistance in corrosion, and eliminate process noise and energy waste. This work is an experimental study of surface parameter optimization during finish end milling of an AA5083 under a specific range of three cutting parameters with an optimized two-flute carbide cutter by previous work. So, twenty-seven experiments were run having varied the radial depth of cut (RDOC), feed rate (f), and cutting speed (S). Surface roughness parameters (Ra and Rt) were measured in the direction of cutting speed at three different distances by the upper edge. The signal-to-noise (SN) ratios have been calculated, and the process was optimized following the analysis of means. Then, additive models with linear interactions were fitted on SN ratios, and the analysis of variances and residual normality plots were utilized to validate the models’ goodness. The SN approach and analysis of means conclude that 0.5 mm RDOC, 6000 rpm speed, and 0.082 mm/tooth feed optimize the process and can effectively predict the Ra and Rt responses. The newly produced machinability data can benefit further applications of AA5083 in industrial applications such as shipbuilding and vehicle bodies.

Single-Cell Screening through Cell Encapsulation in Photopolymerized Gelatin Methacryloyl

This study evaluated the potential of gelatin methacryloyl (GelMA) for single-cell screening compared to polyethylene glycol diacrylate (PEGDA). GelMA photopolymerized at 1000–2000 mJ/cm2 produced consistent patterns and supported HeLa cell viability. GelMA (5%w/v) facilitated better cell collection within 2 days due to its shape retention. GelMA demonstrated biocompatibility with HeLa cells exhibiting exponential proliferation and biodegradation over 5 days. The average cell displacement over 2 days was 16 µm. Two targeted cell recovery strategies using trypsin were developed: one for adherent cells encapsulated at 800 mJ/cm2, and another for floating cells encapsulated at 800 mJ/cm2, enabling the selective removal of unwanted cells. These findings suggest GelMA as a promising biomaterial for single-cell screening applications, offering advantages over PEGDA in cell encapsulation and targeted recovery.

A scoping review of guidelines on caries management for children and young people to inform UK undergraduate core curriculum development

BackgroundCurrent evidence in cariology teaching is not consistently reflected in paediatric dentistry in the United Kingdom (UK). Many dental schools are not consistently teaching biological approaches to caries management, with outdated or complex methods being taught outwith the purview of general dental practitioners. This scoping review aimed to map current guidelines on the management of caries in children and young people. This is part of a work package to inform the consensus and development of a UK-wide caries management curriculum for paediatric dentistry.MethodsA search of electronic databases for peer reviewed literature was performed using Cochrane Library, MEDLINE via PubMed, TRIP Medical Database and Web of Science. Hand searching was undertaken for grey literature (citations of sources of evidence, websites of global organisations and Google Web Search™ (Google LLC, California, USA). Results from databases were screened independently, concurrently by two reviewers. Full texts were obtained, and reviewers met to discuss any disagreement for both database and hand searching.ResultsThis review identified 16 guidelines suitable for inclusion. After quality appraisal, eight were selected for synthesis and interpretation. Key themes included the shift towards selective caries removal and avoidance of complete caries removal unless in specific circumstances in anterior teeth. For “early lesions” in primary and permanent teeth with and without cavitation, several guidelines recommend biological management including site specific prevention and fissure sealants.ConclusionsThis review mapping current cariology guidelines for children and young people found gaps in the literature including classification of early carious lesions and management of early cavitated lesions. Areas identified for further exploration include integration of biological caries management into treatment planning, selective caries removal and whether pulpotomy is specialist-level treatment, requiring referral. These results will inform consensus recommendations in the UK, using Delphi methods.

Selective Removal of Arsenic and Antimony from Pb-Ag Sulfide Concentrates by Alkaline Leaching: Thermodynamic and Kinetic Studies

Arsenic and antimony are impurities that reduce the economic value of concentrates due to the environmental problems they cause. The removal of these impurities by hydrometallurgical means has been highly studied for sulfide copper concentrates using different leaching agents in an alkaline medium (NaClO, H2O2, NaOH, Na2S, NaHS, and S). For a lead–silver concentrate consisting of galena, sphalerite, and pyrite, it was possible to selectively reduce the arsenic content from 1.10% to 0.55% and antimony from 2.41 to 1.04% through the digestion-leaching technique that uses elemental sulfur as a leaching agent in alkaline medium. The adequate powdered sulfur and sodium hydroxide dosage were 336 and 342 kg/t, respectively. The process was carried out at 120 °C with a liquid/solid ratio of 2 in digestion and 5.67 in leaching; the appropriate digestion and leaching time were 20 and 30 min, respectively. The thermodynamics and kinetics of this process turned out to be very complex due to the great variety of simultaneous leaching and precipitation reactions. The digestion process exhibited a mixed kinetic control, where diffusion through the boundary layer and the chemical reaction were the controlling steps with an activation energy of 11.05 kcal/mol.

Purification of soda lignin

Purity of technical lignin is one of the main obstacles in the utilization of lignin to value-added chemicals, products, and materials. The objective of this study was to investigate and compare single and two stage purification methods for obtaining soda lignin with high purity. Extensive washing and extraction with water was found effective, increasing the abundance of acid insoluble lignin while reducing its ash content. Extraction with organic solvents was conducted with 2-propanol or blends of n-heptane/1-butanol or cyclohexane/acetone. These solvents were shown to have little effect on the total lignin content, as determined by wet-chemical methods. Two-stage treatments (washing with water followed by solvent extraction) were hence not better than single stage water extraction in terms of the lignin purity. Still, selective removal of low molecular weight components after solvent extraction was noted, reducing the overall polydispersity of the lignin. Evaporation at 40 °C also showed little effect, whereas calcination at 150 °C significantly increased the molecular weight of the soda lignin. The latter effect was explained by thermally induced cross-linking. In addition, the UV absorbance of the calcinated lignin increased, which is likely related to changes in the aromatic structure. Such effect also entailed that UV/vis spectrophotometry was found less reliable in determining the total lignin content. At last, a mathematical model was adapted to predict the total lignin content from FTIR spectrometry. In conclusion, the tested procedures can be used to purify soda lignin and adjust its molecular weight.

Recent advancements in the application of electrospun nanofibers for carbon dioxide capture and utilization

The escalating CO2 emissions in recent years underlined the need for advanced Carbon Capture and Utilization (CCU) technologies. This context has spurred the exploration of novel materials for promoting CCU efficiency, among which electrospun nanofibers have emerged as a promising candidate. Electrospinning coupled with various post-treatment (such as heat-treating, in-situ growth, selective removal, etc.) offers a versatile approach to fabricate diverse nanofibers, including polymeric, carbonaceous, metallic, and composite fibers, with tunable surface morphologies and chemical properties. This paper provides a comprehensive review of electrospun nanofibers in CCU processes, including adsorption, membrane separation and absorption, electrochemical and photo-electrochemical reduction, thermal catalytic hydrogenation, and more. Each CCU technology is examined in depth to cover the recent research achievements with a specific focus on the contributions of electrospun nanofibers. Lastly, a critical discussion and a list of potential future research directions for this evolving field are provided.