Carbon Nanomaterials Research Articles

Single-Step PECVD Synthesis of Graphene@Carbon Nanotubes Electrocatalyst.

Graphene (Gr) and carbon nanotubes (CNTs), the two intriguing carbon nanomaterials, have presented great potential in serving as high-performance electrocatalysts in lithium-sulfur (Li-S) chemistry. The concurrent management of both materials would achieve a promoted synergistic effect. Nevertheless, there still remains a lack of an effective material synthesis route. Herein, a single-step plasma-enhanced chemical vapor deposition (PECVD) strategy is devised to prepare Gr@CNTs heterostructures with strong bonded connections. In the PECVD system, the damaged sidewalls generated in CNT tubes can serve as appropriate nucleation sites for further Gr growth. The formation mechanisms are thoroughly explored in aspects of both experimental characterizations and theoretical calculations. To confirm the validity of this approach, thus-constructed Gr@CNTs architectures are employed as the sulfur host, enabling boosted redox kinetics of polysulfides. This project provides fundamental insight into the mechanism exploration for single-step PECVD growth of Gr@CNTs heterostructure, hence promoting the practical application prospect of carbon nanomaterials toward Li-S systems.

Copper-catalyzed plastic waste synthesized graphene nanosheets/polypyrrole nanocomposites for efficient thermoelectric applications

Presently, various catalysts have been reported for the synthesis of carbon nanomaterials from a variety of plastic waste, which needs to be removed at the end of the synthesis process by using chemical techniques and hence make the process more typical from the aspect of cost-benefit and circular economic aspects. Herewith, we report copper turnings as the cost-effective and greener catalytic templates for synthesizing highly conducting graphene nanosheets (GNs). The synthesis of the GNs from plastic waste was done as we previously reported in the steps of the pyrolytic process, where the copper turnings are used as catalytic templates in the present study. Because of the excellent catalytic efficiency towards breaking old carbon-carbon bonds and forming new carbon-carbon bonds, the copper turnings act as an excellent degradation catalyst and promote the growth of graphitic skeletons and, consequently, graphene nanosheets. The synthesized GNs showed a high conductivity of ∼ 1730 S/m. GNs thus synthesized is implemented for synthesizing GNs/polypyrrole nanocomposites, which is later investigated for the TE applications. The values of the Seebeck coefficient showed that the composite of GNs/polypyrrole performs as a p-type semiconductor. The TE figure of merit (ZT) for GNs/polypyrrole demonstrated good thermoelectric characteristics and showed a value of 3.75 × 10−6 at the temperature. Thus, the present method of synthesis of GNs showed a more convenient, industrial friendly technique for the production of plastic waste derived graphene nanosheets and its application for thermal energy conversion applications.

Decafluorinated and Perfluorinated Warped Nanographenes: Synthesis, Structural Analysis, and Properties.

Fluorination is a useful approach for tailoring the physicochemical properties of nanocarbon materials. However, owing to the violent reactivity of fluorination, achieving edge-perfluorination of nanographene while maintaining its original π-conjugated structure is challenging. Instead of using traditional fluorination, here, we employed a bottom-up strategy involving fluorine preinstallation and synthesized decafluorinated and perfluorinated warped nanographenes (DFWNG and PFWNG, respectively) through a 10-fold Suzuki-Miyaura coupling followed by a harsh Scholl reaction, whereby precisely edge-perfluorinated nanographene with an intact π-conjugated structure was achieved for the first time. X-ray crystallography confirmed the intact π-conjugated structure and more twisted saddle-shaped geometry of PFWNG compared to that of DFWNG. Dynamic study revealed that the 26-ring carbon framework of PFWNG is less flexible than that of DFWNG and the pristine WNG, enabling chirality resolution of PFWNG and facilitating the achievement of CD spectra at -10 °C. The edge-perfluorination of PFWNG resulted in improved solubility, lower lowest unoccupied molecular orbital, and a surface electrostatic potentials/dipole moment direction opposite those of the pristine WNG. Likely owing to its intact π-conjugated structure, PFWNG exhibits comparable electron mobility with well-known PC61BM. Furthermore, perfluorination improves thermal stability and hydrophobicity, making PFWNG suitable for use as a thermostable/hydrophobic n-type semiconductor material. In the future, this fluorination strategy can be used to synthesize other perfluorinated nanocarbon materials, such as perfluorinated graphene nanoribbons and porous nanocarbon.

Novel sulphur-selective method for simultaneous determination of thiram and asomate based on carbon dots and its application in fruits

Thiram (THI) and asomate (ASO) are frequently detected agrochemicals in food samples due to widespread use as fungicides. However, their detection suffers from matrix interference, or the necessity of derivatization before measurement. Integrating HPLC with a post-column carbon dots (CDs)–enhanced chemiluminescence (CL) system makes it possible to simultaneously separate and selectively detect ASO and THI in fruit samples free of derivatization and deep purification. The studies on mechanisms demonstrated that CD intermediates of anionic radical were responsible for the remarkable CL enhancement of ASO or THI. The CL intensity is directly proportional to the fungicide concentration, with the ranges of linearity for ASO and THI being 5–250 μg·L−1 (R2 = 0.9993) and 4–200 μg·L−1 (R2 = 0.9986), respectively, and the corresponding limits of detection (S/N = 3) being 1.61 and 1.33 μg·L−1, respectively. The developed method enables the exploration of the novelly sulphur-targeted CL application based on carbon nanomaterials.

Enhancing hydrogen storage efficiency: Computational insights into scandium-decorated 2D polyaramid

This study explores hydrogen storage in 2D polyaramid (2DPA) and its enhancement via scandium decoration for onboard storage in fuel cell vehicles. Sc decoration in 2DPA is accompanied by a net 1.6 e charge transfer from Sc to 2DPA. Hydrogen binding in 2DPA + Sc proceeds with a net charge transfer of 0.32 e from Sc towards H2. 2DPA + Sc demonstrates a maximum hydrogen loading capacity of 8.589 wt% with an average adsorption energy of −0.376 eV/H2. These findings meet the stipulated criteria by the US Department of Energy for solid-state hydrogen storage in light-duty vehicles. Feasibility studies were conducted considering practical limitations in transition metal-modified carbon nanomaterials, including Sc-Sc clustering tendencies, stability, and hydrogen desorption behavior via ab initio molecular dynamics simulations, phonon dispersion, and diffusion studies. The highest barrier height for hydrogen desorption from 2DPA + Sc is 0.48 eV, and desorption is predicted to occur at 412 K (5 bar) indicating possibility of room temperature and reversible hydrogen storage. Our findings indicate that 2DPA + Sc is a promising hydrogen storage substrate material and should be explored in experimental trials.

Influence of Graphene, Carbon Nanotubes, and Carbon Black Incorporated into Polyamide Yarn on Fabric Properties

Carbon nanomaterials are increasingly being integrated into modern research, particularly within the textile industry, to significantly boost performance and broaden application possibilities. This study investigates the impact of incorporating three distinct carbon-based nanofillers—carbon nanotubes (CNTs), carbon black (CB), and graphene (Gn)—into polyamide 6 (PA6) multifilament yarns. It explores how these nanofillers affect the physical, mechanical, and thermal properties of PA6 yarns and fabrics. By utilizing melt extrusion, the nanomaterials were uniformly distributed in the yarns, and knitted fabrics were subsequently produced for detailed analysis. The research offers critical insights into how each nanofiller improves the thermal behavior of PA6-based textiles, enabling the customization of their applications. FTIR spectroscopy revealed significant chemical interactions between polyamide and carbon additives, while DSC analysis showed enhanced thermal stability, particularly with the inclusion of graphene. The introduction of these nanomaterials led to increased absorbance and decreased transmittance in the UV-Vis-NIR spectrum. Additionally, Far-Infrared (FIR) emissivity and thermal effusivity varied with different concentrations, with optimal improvements observed at specific levels. Although thermal conductivity decreased with the addition of these nanomaterials, heat management experiments demonstrated varied effects on heat accumulation and cooling times, underscoring potential applications in insulation and cooling technologies. These findings enrich the existing knowledge on nanomaterial-enhanced textiles, providing valuable guidance for optimizing PA6 yarns and fabrics for use in protective clothing, sportswear, and technical textiles. The comparative analysis offers a thorough understanding of the relationship between carbon nanomaterials and thermal properties, paving the way for innovative advancements in functional textile materials.

Heteroatom doped graphitic carbon nanotubes as freestanding anodes for advanced potassium-ion batteries

Owing to its higher earth element reserve and similar chemical properties to lithium, potassium ion batteries (PIBs) have been regarded as a potential alternative to lithium-ion batteries. And considering the relatively larger ionic radius of potassium, available electrode materials need to be equipped with enough space for volume expansion during charge-discharge cycles, thus graphitic carbon nanomaterials with adjustable layer spacing gradually come into researcher's version. Here with copper nanowires serving as growth template and organic polyvinyl pyrrolidone (PVP) providing carbon source, freestanding and ultra-light graphitic carbon nanotube (GCNT) aerogels were simply assembled and annealed, which were directly used as anodes of PIBs. Annealing parameters (temperature and atmosphere) were adapted to regulate the lattice order and interlayer spacing of GCNTs, and N, O heteroatoms derived from PVP were directly doped into the carbon lattice during thermal annealing, to optimize and enhance the cycle capacity and rate performance of GCNT anodes. The electrochemical potassium storage mechanism of GCNTs was also quantitatively analyzed. Most of the potassium ions are reversibly stored by squeezing into and escaping from the carbon lattice, and simultaneously oxygen-containing functional groups with different chemical states also offer active redox sites and dedicate partial capacity. Therefore, our assembled GCNTs with large lumen are expected to sandwich-like load with active substances efficiently, further constructing next-generation PIBs with excellent performance.

Electrochemical characterization of carbon black in different redox probes and their application in electrochemical sensing

Carbon black - materials rich in carbon nanostructures - have been successfully applied as modifiers of electrochemical transducers, rivalling other carbon nanomaterials for cost and ease-of-use. Despite the remarkable promise of this nanomaterial, no study has yet comparatively characterised a wide range of different grades of carbon black for their utility in electrochemical sensors. Here, we explore several commonly-studied carbon black grades (N220, N234, N326, N330, N339, N375, N550, N660 and Lamp Black-101), alongside relatively newer grades (Printex®-200, Printex® G, Printex® XE-2B, and Printex® Zeta) for their application in electrochemical sensors. The effects of coating glassy carbon electrodes with carbon black on electrode performance were studied by cyclic voltammetry using three redox probes: ferri-/ferrocyanide (anionic probe molecules), ferrocenemethanol (neutral) and hexaammineruthenium (cationic). Raman Spectroscopy characterisation of the different grades associated a lower degree of graphitisation with superior electrode modifiers. Generally, modification increased the anodic peak current for ferri-/ferrocyanide probes; and lowered anodic potential for ferri-/ferrocyanide and hexaammineruthenium probes. Increases in peak current and potential observed at ferrocenemethanol are consistent with the increased tendency for this probe to adsorb to the surface of modified electrodes. N330 and Printex® XE-2B displayed the best electrocatalytic properties in terms of enhanced peak currents and lowered anodic overpotentials for the redox probes. CB grades were used to modify screen-printed carbon electrodes and the obtained sensors examined for anodic detection of reduced nicotinamide adenine dinucleotide (NADH) cofactor by cyclic voltammetry. Printex® XE-2B significantly improved the detection of NADH and was further used for chronoamperometric detection of NADH at low overpotentials. Grades N220, N375, N550 and P-G showed their suitability as enzyme scaffolds for sensor fabrication, as determined by their preservation of the activity of a NAD-dependent aldehyde dehydrogenase.

Fluorinated aggregated nanocarbon with high discharge voltage as cathode materials for alkali-metal primary batteries.

Due to its exceptionally high theoretical energy density, fluorinated carbon has been recognized as a strong contender for the cathode material in lithium primary batteries particularly valued in aerospace and related industries. However, CF x cathode with high F/C ratio, which enables higher energy density, often suffer from inadequate rate capability and are unable to satisfy escalating demand. Furthermore, their intrinsic low discharge voltage imposes constraints on their applicability. In this study, a novel and high F/C ratio fluorinated carbon nanomaterials (FNC) enriched with semi-ionic C-F bonds is synthesized at a lower fluorination temperature, using aggregated nanocarbon as the precursor. The increased presence semi-ionic C-F bonds of the FNC enhances conductivity, thereby ameliorating ohmic polarization effects during initial discharge. In addition, the spherical shape and aggregated configuration of FNC facilitate the diffusion of Li+ to abundant active sites through continuous paths. Consequently, the FNC exhibits high discharge voltage of 3.15V at 0.01C and superior rate capability in lithium primary batteries. At a high rate of 20C, power density of 33,694Wkg-1 and energy density of 1,250Wh kg-1 are achieved. Moreover, FNC also demonstrates notable electrochemical performance in sodium/potassium-CF x primary batteries. This new-type alkali-metal/CF x primary batteries exhibit outstanding rate capability, rendering them with vast potential in high-power applications.

Water dispersible carbon nanomaterials reduced N, P, and K leaching potential in sandy soils: A column leaching study

Carbon nanomaterials (CNMs) — amendments with carbon in nanoscale form —could potentially enhance fertilizer delivery efficiency in agriculture, but their interaction with soil properties and nutrient co-mobility, especially in coarse-textured soils, remain poorly understood. We conducted a column leaching study in repacked soil columns to compare the co-leaching of novel water-dispersible CNMs and soil nutrients across two levels of CNMs applications (200 & 400 mg kg−1), two fertilization rates (low:80 mg kg−1 of N, P and K and high: 200 mg N kg−1, 100 mg P kg−1, 200 mg K kg−1, applied as ammonium nitrate, potassium phosphate, and potassium nitrate) and two soils (Spodosol with pH = 5.1, Alfisol with pH = 6.5). We imposed 12 leaching events to each column, with each leaching event adding water equivalent to the soil-pore volume (250 mL), resulting in cumulative leaching of 3000 mL of water through each column. CNMs applications reduced cumulative leaching losses of NO3-N (Spodosol: 8–12 %, Alfisol: 9–19 %), NH4-N (Spodosol: 2–14 %, Alfisol: 9–14 %), P (Spodosol: 23–27 %, Alfisol: 23–36 %) and K (Spodosol: 17–23 %, Alfisol: 24–26 %) compared to fertilized columns without CNMs. CNMs increased soil pH by up to 0.3 units (Spodosol) or 0.5 units (Alfisol), while lowering electrical conductivity by 15–20 % at the high fertilization rate in both soils. Columns with water-dispersible CNMs accumulated 25–30 % more total C in the base sections of the Alfisol compared to the Spodosol, indicating faster downward movement through the soil profile. Overall, we demonstrated that CNMs have the potential to reduce nutrient leaching in coarse-textured soils, which could be particularly beneficial in high-input intensive agricultural systems.

Application of Carbon Nanomaterials to Enhancing Tumor Immunotherapy: Current Advances and Prospects.

Recent advances in tumor immunotherapy have highlighted the pivotal role of carbon nanomaterials, such as carbon dots, graphene quantum dots, and carbon nanotubes. This review examines the unique benefits of these materials in cancer treatment, focusing on their mechanisms of action within immunotherapy. These include applications in immunoregulation, recognition, and enhancement. We explore how these nanomaterials when combined with specific biomolecules, can form immunosensors. These sensors are engineered for highly sensitive and specific detection of tumor markers, offering crucial support for early diagnosis and timely therapeutic interventions. This review also addresses significant challenges facing carbon nanomaterials in clinical settings, such as issues related to long-term biocompatibility and the hurdles of clinical translation. These challenges require extensive ongoing research and discussion. This review is of both theoretical and practical importance, aiming to promote using carbon nanomaterials in tumor immunotherapy, potentially transforming clinical outcomes and enhancing patient care.

Temperature-dependent highly active LaCaMgAl2O4 catalyst effect on carbon nanomaterial and hydrogen generation from polymethyl methacrylate plastic

The increasing accumulation of waste polymethyl methacrylate (PMMA) plastics presents a significant environmental challenge, while the demand for renewable energy sources continues to rise. Thermochemical recycling is a prospective technique for converting waste plastics into high-value chemicals, both economically and environmentally. In this work, the catalytic pyrolysis of waste PMMA plastics over LaCaMgAl2O4 nanosheets (NSs) catalyst is being investigated for its potential to produce hydrogen and carbon nanotubes (CNTs) in a two-stage fixed-bed reactor. The yield and purity of the gaseous products, as well as carbon deposition, concerning the effects of temperature during the catalysis process. Additionally, a small portion of LaCa was incorporated into the MgAl2O4 composite in the pre-catalysts under investigation. Analyzing the physicochemical properties of the carbon nanomaterials that form provides valuable insights into the workings of different catalysts. It's noteworthy that LaCaMgAl2O4 NSs showed such large yields of H2 (82.71 vol% H2) and CNTs (388 mg g−1) at 750 °C. The LaCaMgAl2O4 NSs catalyst's impressive ability to produce CNTs and H2 gas at high yields underscores its efficacy and potential for real-world catalytic pyrolysis applications. This study emphasizes the Nanocatalyst's potential for large-scale catalytic pyrolysis operations, providing a workable and efficient way of converting waste plastics into high-value products and renewable energy.

Preparation and characterisation of IPMC brakes modified with composite electrodes performance

Ionic Polymer Metal Composite (IPMC) can be used as flexible actuators and sensors in the fields of bionic machinery and medical devices. However, IPMC still suffer from poor actuation performance and high cost of electrode preparation in practical applications. Optimisation of electrodes and use of novel assembly processes are expected to solve these problems. In this paper, low-dimensional nanocarbon materials were used to modify the Nafion membrane. Appropriate amounts of carbon nanotubes and carbon black were weighed and dispersed in chitosan and acetic acid to form a stable electrolyte. A new IPMC was prepared by bonding carbon nanotube and carbon black films on the Nafion membrane using the hot pressing method. Scanning electron microscope images showed that the hybrid films composed of carbon nanotubes and carbon black were successfully hot pressed onto the surface of the Nafion membrane and the hybrid electrode layer composed of carbon nanotubes and carbon black was more homogeneous and densely packed. The results of driving performance tests show that the hybrid electrode-modified IPMC has excellent driving performance, with a maximum output displacement of 9.2 mm and a maximum output force of 9.9 mN at a voltage of 5.0 V. These results are 1.07 and 1.14 times higher than those of the carbon nanotube IPMC and 1.74 and 1.70 times higher than those of the carbon black IPMC under the same conditions, respectively.

Fabrication of PVC-based electromagnetic interference shielding composite film by positively charged SMA enhancing the dispersibility of carbon nanomaterial

To address the weak binding force and poor dispersion stability of carbon (C) nanoparticles in current non-covalent modification methods, we employed organic amine-grafted styrene maleic anhydride copolymers (SMA-N) to modify C nanoparticles (C@SMA-N) through π–π conjugation and positive charge interactions. The obtained C@SMA-N has excellent dispersion in N, N-dimethylacetamide (DMAc), which is attributed to the enhanced steric hindrance and electrostatic repulsion from the grafted organic amine chains. To study the impact of surface modification on the electromagnetic interference shielding effectiveness (EMI SE), C@SMA-N was used as a conductive filler in polyvinyl chloride (PVC) composite films, which exhibits a higher EMI SE performance than pristine C nanoparticles. Particularly, the obtained C@SMA-N using polyether amine (PEA) (C@SMA-PEA) exhibits a better EMI SE performance. By optimizing the SMA-PEA grafting parameters, the PVC/C@SMA-PEA composite films transition from insulators to conductors at a C@SMA-PEA content of 0.3 wt%. To achieve a higher EMI SE performance, the filler content, mixed filler composition, and film thickness were optimized. The results indicate that with a total filler content of 20 wt% and a mixed filler comprising fibrous form carbon nanotubes (CNT) and particles form carbon black (CB) in a 10:1 mass ratio (CB@SMA-PEA to CNT@SMA-PEA), the composite film has a thickness of 0.08 mm and an EMI SE value of 20.2 dB. Increasing the thickness to 0.2 mm enhances the EMI SE value to 31.5 dB. These findings indicate that thinner films have a higher EMI SE performance and promising application prospects in the field of electromagnetic shielding.

Field-deployable pencil lead-based electrochemical cell for the determination of the emerging contaminant and antidepressant drug venlafaxine in wastewater

Screening and quantification of emerging contaminants in water is of enormous relevance due to its scarcity and harmful effects on aquatic life and human health. We present a simple and cost-effective electrochemical cell for determination of the antidepressant venlafaxine, an emerging contaminant included in the EU Watch List 2022. The cell consists of pencil leads used as electrodes and a microcentrifuge tube. Modification of the working electrode with carbon nanomaterials improved the signal. Cell-related parameters (e.g., type of pencil leads or electroactive area) as well as experimental (e.g., pH, accumulation potential and time, and scan rate) were thoroughly optimized. The adsorptive nature of venlafaxine process allowed the use of adsorptive stripping square wave voltammetry methodology to increase the sensitivity. Under optimized variables, a linear range from 0.8 to 10 μmol L-1, with a correlation coefficient of 0.996 and a sensitivity of 1.48 μmol L-1, a LOD of 0.4 μmol L-1 and a RSD of 2.4 % were achieved. Selectivity was also studied, especially with respect to the main metabolite o-desmethylvenlafaxine. The methodology distinguishes its signal from that of the main compound, allowing its determination. A similar linear range was obtained for the metabolite, with a LOD of 0.6 μmol L-1. The platform developed was applied for venlafaxine quantification in spiked wastewaters from the Febros plant in Portugal, obtaining satisfactory recoveries. Furthermore, the versatility of pencil leads made it possible to combine them with modified paper for sampling and buffering in order to decentralize the determination, showing promising results.

Nitrogen functionalized biomass derived mesoporous carbon nanomaterials for electrochemical detection of lead (II) ions

This study has explored the sustainable solution after designing an economical metal-free biomass-derived nanocarbon for the selective sensing of lead. The nitrogen and sulfur-rich mesoporous nanocarbon is designed through a facile hydrothermal-assisted thermal annealing method. The high-temperature treatment gave nanocarbon unique carbon dot decorated layered morphology, while nitrogen and sulfur precursor thiourea and melamine strengthened the nanomaterial stability, sensitivity, and selectivity toward lead metal ions. The high specific surface area of mesoporous nanocarbon viz., 1671.93 m2/g with the pore width and pore volume of 2.02 nm and 0.476 cm3/g has enhanced the conductivity of as-synthesized sensor, which helps in increasing sensitivity toward lead. The high conductivity was also confirmed through cyclic voltammetry, where an 80 % increment in current was observed in the case of the modified electrode when compared with bare GCE. The differential pulse normal voltammetry and differential pulse anodic stripping voltammetry were performed to calculate the detection limit, where an excellent detection limit of 22 nM was obtained from the DPASV technique. Moreover, the nanomaterial was also tested for detecting lead in tap water. The as-synthesized nanocomposite is highly efficient and selective for the detection of lead. This study will motivate the researchers to engineer sustainable and efficient devices for sensing metal pollutants.

Multi-pollutant degradation from 2D MoO3/g-C3N4/functional carbon nanomaterial based composite utilizing Z-scheme photocatalysis

In this report, photocatalysis, an advance oxidation process (AOPs) is considered to be the most suitable for degrading dye pollutant like acriflavine and methylene blue via Z-scheme catalysis. Current vivid study converges the role of 2D MoO3/g-C3N4 modified with green-precursor derived functional carbon nanomaterial (FCM). The morphological, structural and optical features of the composite were analysed using XRD, FESEM, EDX, FTIR, UV–VIS, Raman spectroscopy whereas its photocatalytic activity was assessed for the degradation of a pharmaceutical (acriflavine) and a textile (methylene blue) dye. The biocompatibility, reusability, chemical, thermal and hydrothermal stability of g-C3N4 and FCM when complemented with 2D-MoO3 for improved charge transport and enhanced surface area including Z-scheme catalysis, results in a stable and an abundant reaction for nearly 100 % degradation of acriflavine in just 60 min and 94 % degradation of methylene blue (MB) in 100 min under visible light. This efficiency is found to be less than 60 % for each material when used stand-alone. Further, the demonstration of efficient visible range utilization (from 300 to 500 nm) by the composite that exhibits up-conversion as well as broad photoluminescence from FCMs in its nano-dimension form, is observed. Possible effect of internal electric field which reduces the electron-hole recombination, the suitable band positions for Z-scheme charge transfer, ease of production and scaling up, cost effectiveness and multi-dye degradation study suggest that the proposed composite is highly suitable in the family of photocatalysis for environmental cleaning of multiple cationic dyes.

Carbohydrate-Derived Superhydrophilic Carbon Aerogels and Their Effects on Seedling Growth of Triticum aestivum.

Synthesis methods of carbon nanomaterials have been developed vigorously in recent years, among which a simple, green, and mature approach is of more research significance. Carbon nanomaterials have depicted an impact on the growth and development of plants. In this study, a new type of carbon nanomaterial, superhydrophilic carbon aerogel (CA), was synthesized via a hydrothermal process using carbohydrates and water-soluble polymers as raw materials. Characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, powder X-ray diffraction, and N2 adsorption analysis, the exemplified CA presented to have porous three-dimensional network structure composed of individual particles with diameters of 25 nm, with reactive surface, single composition, high specific surface area (89.94 m2·g-1), and wide range of density variation. The 9 mg·mL-1 CA suspension had a significant positive effect on the root growth of wheat seedlings, with promoted root elongation (about 67.17% longer) and root diameter (about 28.95% thicker) compared with those of the control group. The cytological results suggested that CA treatment triggered the propagation of meristematic cells, and the increased number of meristematic cells (65.79% more than the control group) led to enhanced root growth by upregulated expression of related phytohormone genes in wheat seedlings.

Enhancing anaerobic digestion of food waste for biogas production: Impact of graphene nanoparticles and multiwalled nanotubes on direct interspecies electron transfer mechanism

The present research investigated the effect of two carbonaceous materials, multiwalled carbon nanotubes (MWCNTs), and graphene nanoparticles (GNPs), on biogas yield from food waste (FW) in an anaerobic digestion system for 30 days. Lab scale investigations were conducted in batch mode in 250 mL glass reactor bottles and the findings were compared to the control reactor. The performance of the experimental procedure was assessed in terms of biogas output and organic matter reduction. The addition of 100 mg/L multiwalled carbon nanotubes and 100 mg/L GNPs increased the cumulative biogas production (33.55 % and 81.16 %, respectively) while decreasing the total solid content (about 25.95 % and 24.95 %, respectively). However, increasing the concentration of both carbon nanomaterials from 100 mg/L to 500 mg/L reduced the total biogas production compared to the control, which can be attributed to cytotoxic effects. A microbial diversity study was performed using 16S amplicon sequencing to understand the changes occurring in the microbial ecology. The predominant phyla found during diversity analysis were Firmicutes, Proteobacteria, Actinobacteriota, and Bacteroidota. Finally, addition of carbonaceous nanomaterials to the anaerobic reactors favours organic matter degradation through the DIET mechanism. It improves the biogas production kinetics and productivity during the anaerobic digestion of FW up to a certain dose.

A sustainable approach for efficient ammonium recovery, and simultaneous TOC removal from aqueous solutions by vesicle-like iron phosphate-based carbon nanomaterials

NH4+ is an ion with versatile potential; however, the release of wastewater containing this component, regardless of its high or low concentration, causes severe eutrophication in aquatic systems and contaminates numerous manufacturing processes. Thus, this study developed a sustainable method that can simultaneously remove, recover NH4+, polish water, oxidize organic matter, and yet release a material that can still be used as fertilizer. Regarding NH4+ removal, FeP400 rapidly exhibited an exceptional NH4+ uptake capacity (343.5 mg g-1) within 8 min, even in dairy processing wastewater with high NH4+ concentrations and diverse co-existing components. FeP400 could oxidize organic compounds spontaneously to remove TOC, indirectly enhancing its NH4+ uptake up to 33.5 % through charge balance mechanisms. The adsorption process involved both chemical (i.e., double-salt precipitation) and physical mechanisms (i.e., H-bonding and electrostatic interaction), as confirmed by thermodynamics, FT-IR, and XPS analyses. Regarding recovery, FeP400 can be reused for over 10 cycles with high removal (81 %) and NH4+ recovery (88 %), a significant improvement over conventional options. FeP400 also performed efficiently under flowing conditions using low-range NH4+ and TOC samples over 10 cycles, polishing not only 34.1 L of water with undetected NH4+, neutral pH, and extremely low TOC but also effectively recovering the NH4+ uptake at an economical cost. Lastly, its environmentally friendly nature, which contains essential nutrients for plant growth, further enhances its recyclability after release. Thus, FeP400 is believed to offer a transformative, sustainable, and highly efficacious solution to the NH4+contamination and critical ultrapure water issues that industries urgently address.