Pristine Multi-walled Carbon Nanotubes Research Articles

Poly(aniline)-multiwall carbon nanotube (PANI@MWCNT) composite as high-cost Pt free counter electrode for dye-sensitized solar cells

In this study, we synthesized a poly (aniline)-multiwall carbon nanotube (PANI@MWCNT) composite for use as a counter electrode (CE) in dye-sensitized solar cells. Moreover, FE-SEM and HR-TEM images of PANI@MWCNT revealed carbon nanotube/ropes embedded in the polymer matrix. An X-ray diffraction pattern confirmed the amorphous nature of the composite. Further, Electrochemical impedance spectroscopy studies indicated a charge transport resistance value (Rct) of 4.36 KΩ for PANI@MWCNT. CV studies demonstrated improved electrocatalytic performance and faster redox behavior in the PANI@MWCNT composite. BET analysis measured the pore size of the as-prepared composite to be 15–50 nm. Subsequently, the as-synthesized PANI, PANT@MWNCT, pristine MWCNT, and platinum were evaluated as CEs in DSSCs using a polyethylene oxide polymer-based liquid electrolyte and a TiO2 nanocrystalline photoanode. Among these CEs, the PANI@MWCNT CE exhibited an efficiency of 8.07 %, and the stability test indicated that the as-prepared composite CE retained 7.81 % efficiency after 15 days.

Structural and morphological studies of non-covalent functionalization carbon nanotubes wrapped poly(3-hexylthiophene-2,5-diyl) nanocomposites

In this study, a simple and efficient non-covalent functionalization method was developed to introduce conducting polymer of P3HT onto pristine MWCNT and hydroxyl MWCNT surfaces without causing significant changes in electrical characteristics, especially if used as a sensing material. Electron microscopy (FE-SEM) and (HR-TEM) were used to examine the surface morphology of nanocomposites, which demonstrated that the MWCNTs were well wrapped by P3HT. EDX analysis showed interactions between MWCNT-OH and P3HT, with a higher sulfur content of 7.77 wt% from P3HT. Additionally, the diameters of both pristine MWCNT (24.46 nm) and MWCNT-OH (27.56 nm) increased significantly when they form nanocomposites (35.35 nm and 39.40 nm respectively). Further characterization of the produced P3HT-MWCNT nanocomposite was performed using FT-IR and Raman spectroscopy. It was discovered that MWCNTs were dispersed uniformly, with a substantial interaction between P3HT and MWCNTs. The introduction of malathion on the surface of the nanocomposites reveals interaction between P3HT and malathion via intermolecular hydrogen bonding of thiophene, as evidenced by inelastic neutron scattering (INS) spectroscopy, suggesting that the P3HT/MWCNT has the potential as a promising sensing material for organophosphate compounds detection.

Enhanced Dye Adsorption on Cold Plasma-Oxidized Multi-Walled Carbon Nanotubes: A Comparative Study.

The oxidation of multi-walled carbon nanotubes (MWCNTs) using cold plasma was investigated for their subsequent use as adsorbents for the removal of dyes from aqueous solutions. The properties of MWCNTs after plasma modification and their adsorption capacities were compared with pristine and chemically oxidized nanotubes. The modification process employed a reactor where plasma was generated through dielectric barrier discharges (DBD) powered by high-voltage nanosecond pulses. Various modification conditions were examined, such as processing time and pulse voltage amplitude. The degree of oxidation and the impact on the chemistry and structure of the nanotubes was investigated through various physicochemical and morphological characterization techniques (XPS, BET, TEM, etc.). Maximum oxidation (O/C = 0.09 from O/C = 0.02 for pristine MWCNTs) was achieved after 60 min of nanopulsed-DBD plasma treatment. Subsequently, the modified nanotubes were used as adsorbents for the removal of the dye methylene blue (MB) from water. The adsorption experiments examined the effects of contact time between the adsorbent and MB, as well as the initial dye concentration in water. The plasma-modified nanotubes exhibited high MB removal efficiency, with adsorption capacity proportional to the degree of oxidation. Notably, their adsorption capacity significantly increased compared to both pristine and chemically oxidized MWCNTs (~54% and ~9%, respectively). Finally, the kinetics and mechanism of the adsorption process were studied, with experimental data fitting well to the pseudo-second-order kinetic model and the Langmuir isotherm model. This study underscores the potential of plasma technology as a low-cost and environmentally friendly approach for material modification and water purification.

5 MeV Si ion irradiation effects on structural and morphological properties of multiwalled carbon nanotubes

Carbon based nanomaterials (CBNs) such as multi walled carbon nanotubes (MWCNTs), graphene etc have attracted huge interest due to their widespread applications in contemporary nanotechnology. The ion bombardment is an important method which can be used for tuning of the structural and morphological properties of the CBNs. In the present work, we have carried out ion irradiation on MWCNTs (prepared by chemical vapour deposition method) with 5 MeV Si ions at different fluences ranging from 1 × 1014 to 5 × 1016 ions/cm2. The resulting structural and morphological modifications on the pristine MWCNTs have been characterized by using X-ray diffraction, Raman spectroscopy and field emission scanning electron microscopy. Results observed after successful characterization are compared with pristine sample results and we observed that the irradiation creates defects in MWCNTs and causes amorphized carbon nanomaterials depending on the fluence and energy deposited by energetic ions inside the MWCNTs.

In silico-guided discovery and in vitro validation of novel sugar-tethered lysinated carbon nanotubes for targeted drug delivery of doxorubicin

ContextMultiwalled carbon nanotubes (MWCNTs) functionalized with lysine via 1,3-dipolar cycloaddition and conjugated to galactose or mannose are potential nanocarriers that can effectively bind to the lectin receptor in MDA-MB-231 or MCF-7 breast cancer cells. In this work, a method based on molecular dynamics (MD) simulation was used to predict the interaction of these functionalized MWCNTs with doxorubicin and obtain structural evidence that allows a better understanding of the drug loading and release process. The MD simulations showed that while doxorubicin only interacted with pristine MWCNTs through π-π stacking interactions, functionalized MWCNTs were also able to establish hydrogen bonds, suggesting that the functionalized groups improve doxorubicin loading. Moreover, the elevated adsorption levels observed for functionalized nanotubes further support this enhancement in loading efficiency. MD simulations also shed light on the intratumoral pH-specific release of doxorubicin from functionalized MWCNTs, which is induced by protonation of the daunosamine moiety. The simulations show that this change in protonation leads to a lower absorption of doxorubicin to the MWCNTs. The MD studies were then experimentally validated, where functionalized MWCNTs showed improved dispersion in aqueous medium compared to pristine MWCNTs and, in agreement with the computational predictions, increased drug loading capacity. Doxorubicin-loaded functionalized MWCNTs demonstrated specific release of doxorubicin in tumor microenvironment (pH = 5.0) with negligible release in the physiological pH (pH = 7.4). Furthermore, doxorubicin-free MWNCT nanoformulations exhibited insignificant cytotoxicity. The experimental studies yielded nearly identical results to the MD studies, underlining the usefulness of the method. Our functionalized MWCNTs represent promising non-toxic nanoplatforms with enhanced aqueous dispersibility and the potential for conjugation with ligands for targeted delivery of anti-cancer drugs to breast cancer cells.MethodsThe computational model of a pristine carbon nanotube was created with the buildCstruct 1.2 Python script. The lysinated functionalized groups were added with PyMOL and VMD. The carbon nanotubes and doxorubicin molecules were parameterized using the general AMBER force field, and RESP charges were determined using Gaussian 09. Molecular dynamics simulations were carried out with the AMBER 20 software package. Adsorption levels were calculated using the water-shell function of cpptraj. Cytotoxicity was evaluated via a MTT assay using MDA-MB-231 and MCF-7 breast cancer cells. Drug uptake of doxorubicin and doxorubicin-loaded MWCNTs was measured by fluorescence microscopy.

Isotherm and kinetics study of Ni(II) ions adsorption from wastewater using carbon nanotubes decorated with ZnO nanoparticles

A zinc oxide/carbon nanotube hybrid (ZnO/MWCNT) was synthesized utilizing a straightforward precipitation technique based on the physical approach of pulsed laser ablation. Various techniques were employed to investigate the composition, morphology and optical of the synthesized nanocomposite. The techniques employed were X-ray diffraction, Raman spectroscopy, transmission electron microscopy, FT-IR and thermal gravimetric analysis (TGA) to confirm the compete decoration to be applicable for removal Ni(II) ions in an aqueous solution. ZnO have a hexagonal wurtzite structure connected to hexagonal graphite of MWCNT from XRD. The interaction between ZnO and CNTs resulted in a reduction in the domain of sp2 bonds, according to Raman. From TGA, we can attribute the reduction in thermal analysis to the oxidation of surface hydroxyl functional groups (-OH), the evaporation of surface solvent and the presence of ZnO’s inorganic oxide structure compared to pristine MWCNT. These findings confirmed that adding ZnO NPs to MWCNT caused more structural flaws and surface disorder, even though the structure of the CNTs stayed the same. We then investigated numerous factors affecting the extraction of Ni(II) ions, including pH, duration of extraction, amount of nanosorbent used and circumstances. We observed the optimal conditions at room temperature, pH of 5.9, nanoadsorbent dosage of 0.2 g/L and contact time of 1 h. Atomic absorption spectrometry easily monitored the kinetics of this reaction. The Langmuir, Freundlich and Redlich–Peterson isotherm models explain the mechanism underlying the adsorption equilibrium isotherm. Furthermore, regeneration experiments revealed that the adsorbent still maintained a high adsorption capacity after six cycles, demonstrating remarkable potential for use in environmentally friendly applications.

Synthesis of Ag/NiFe2O4 doped multiwalled carbon nanotube for antibiotic removal from water

Antibiotics impose severe impacts on humans and the ambient water environment by creating antimicrobial resistance in bacterial pathogens; therefore, there exists an urgent need to develop sustainable and efficient adsorbents for the removal of these contaminants from the water. To this goal, silver/nickel ferrite-doped multiwalled carbon nanotubes (Ag/NiFe2O4 doped MWCNTs) were prepared as functional integrated adsorbent material for antibiotic removal from water. The TEM results showed that Ag/NiFe2O4 species were dispersed on the surface of MWCNTs through the available functional groups on their surface. The introduction of Ag/NiFe2O4 nanocomposite onto the MWCNTs efficiently improved the adsorption capacity for ciprofloxacin. The maximum adsorption capacity is estimated to be 26.45 mg/g. The results indicated a higher adsorptive capacity for the produced ternary sample compared to pristine MWCNTs, Ag/NiFe2O4, or NiFe2O4/MWCNTs binary systems. The adsorption capacity for ciprofloxacin in the samples was evidently dependent on the MWCNTs dose, solution pH, adsorbate dose, and temperature. Ag/NiFe2O4 doped MWCNTs (65 % w/w) were able to remove ∼95 % of ciprofloxacin in the testing solution even after being reclaimed for 4 times following the Langmuir isotherm model in the endothermic manner. Also, the adsorption of CIP by the nanocomposite demonstrates a pseudo-second-order model. These promising results open a pathway for efficient carbon materials to be replaced by conventional adsorbents to remove antibiotics from water.

Ligand Exchange Reaction between Ferrocene and Multiwalled Carbon Nanotubes: A Contemporary Approach.

Ligand exchange reaction (LER) between carbon nanoparticles and ferrocene (Cp2Fe) was conducted several times, but there was no convincing evidence of half-sandwich CpFe+ coordination to multiwalled carbon nanotubes (MWCNT). In this study, MWCNT is modified by LER with ferrocene using AlCl3/Al as a catalytic system. The modified MWCNT (Fc-MWCNT) are investigated for better understanding of the processes taking place on the surface of MWCNT using different spectroscopic and electrochemical methods. The formation of the Fe-C covalent bond between CpFe+ and MWCNT is confirmed by changes in the Raman spectrum of Fc-MWCNT compared to pristine MWCNT. The densest structure of Fc-MWCNT is investigated by transmission electronic microscopy. According to density-functional theory calculations of the model interaction between Fe and coronene, the Fe-C bond length is 2.1687-2.1855 Å. X-ray photoelectron spectroscopy also confirms the coordination of the Fe atom to MWCNT by analysis of oxidation states of Fe 2p and deconvolution of C 1s. Utilization of cyclic voltammetry corroborated MWCNT modification via LER. These data are important for both theoretical and practical applications due to increased interest in LER-modified compounds in different areas including thermoelectric devices, sensors, and its potential application in the field of molecular machine construction.

Eco-friendly Functionalization of MWCNTs with Deep Eutectic Solvents

The unique features of deep eutectic solvents (DESs) have sparked interest in their use for various applications due to their capacity to introduce new functional groups and other surface alterations. In this study, DESs were employed for the surface modification of MWCNTs. Twelve distinct varieties of Choline chloride-based DESs were prepared and characterized. Prior to the MWCNTs functionalization process, further tests, including viscosity, density, and TGA analysis, were carried out to evaluate the stability of the prepared solvents. The surface functionalization of MWCNTs was then carried out using the most stable solvent. The DESs-functionalized samples were tested for dispersibility and solubility, and FTIR was used to confirm the functional groups present. In comparison to the pristine MWCNTs, the result showed that samples D1, D2, and D4 had several functional groups on their surfaces. Also, in comparison to other DESs-functionalized samples, D1, D2, and D4 had more oxygen-containing groups, as further corroborated by CHNS analysis.As a result, DESs comprising glycerol and ethylene glycol provide an environmentally benign route to alter the surface of MWCNTs, making them suitable functional materials for a range of uses such as Adsorbents, Catalysts, Li batteries, EMI shielding materials, and Supercapacitor electrolytes.

Enhanced Adsorption of Methylene Blue Dye on Functionalized Multi-Walled Carbon Nanotubes.

Carbon nanomaterials are promising adsorbents for dye removal from wastewater also due to their possible surface functionalization that, in principle, can increase the adsorption rate and provide regeneration. To investigate the real advantages of functionalization, we synthesized and characterized through IR, TGA, TEM, XPS and DLS measurements a multi-walled carbon nanotube (MWCNT) derivative bearing benzenesulfonate groups (MWCNT-S). The obtained material demonstrated to have good dispersibility in water and better capability to adsorb methylene blue (MB) compared to the pristine MWCNT adsorbent. Adsorption kinetic studies showed a very fast process, with a constant significantly higher with respect not only to that of the unfunctionalized MWCNT adsorbent but also to those of widely used activated carbons. Moreover, the adsorption capacity of MWCNT-S is more than doubled with respect to that of the insoluble pristine MWCNT adsorbent, thanks to the dispersibility of the derivatives, providing a larger available surface, and to the possible electrostatic interactions between the cationic MB and the anionic sulfonate groups. Additionally, the reversibility of ionic interactions disclosed the possibility to release the adsorbed cationic pollutant through competition with salts, not only regenerating the adsorbent, but also recovering the dye. Indeed, by treating the adsorbed material for 1 h with 1 M NaCl, a regeneration capacity of 75% was obtained, demonstrating the validity of this strategy.

PLLA/(MWCNTs-ZnO)@PDA composite with NIR-light induced shape memory effect, antibacterial properties and 3D printability

PLLA based shape-memory polymer composites with multifunctions have attracted growing attention in biomedical applications. Generally, a single nanofiller has the problem of insufficient functionalization and easy aggregation. Therefore, we design and fabricate polydopamine (PDA) surface modified MWCNTs-ZnO hybrid nanostructure ((MWCNTs-ZnO)@PDA). The dispersion of (MWCNTs-ZnO)@PDA in PLLA is improved in comparison with the pristine MWCNTs or ZnO. The results indicate that the (MWCNTs-ZnO)@PDA nanosystem shows a synergistic effect on the mechanical properties and photothermal properties of the composites. Comparative analysis with neat PLLA demonstrates a remarkable 17% increase in tensile strength and a 19% increase in elongation at break for PLLA/(MWCNTs-ZnO)@PDA composite. Additionally, the composites exhibit excellent NIR light-induced shape memory effects with a shape recovery ratio reaching 100%. Moreover, PLLA/(MWCNTs-ZnO)@PDA composites show favorable antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). Furthermore, the polymer composites display good 3D printability, and the 3D-printed porous scaffold possesses high compressive strength and modulus. Also, the PLLA/(MCNTs-ZnO)@PDA scaffold can be compressed into a compact size and recover its original shape under NIR light irradiation. This work provides an approach to prepare novel shape-memory polymer composites with multifunctions including high strength, light-induced shape-recovery, antibacterial properties and printability.

Chloride penetration resistance of ultra-high performance concrete with various multi-walled carbon nanotubes

Ultra-high performance concrete (UHPC) with outstanding chloride penetration resistance (CPR) exhibits excellent prospects for extending the service life of structures in the marine environment. This study investigates the effects of various types and contents of multi-walled carbon nanotube (MWCNT) on the CPR of UHPC, including pristine MWCNT with different sizes, MWCNT with surface modification, and MWCNT with special structures. The results show that 0.25% thick-short pristine MWCNT, 0.5% short hydroxyl functionalized MWCNT, and 0.25% helical MWCNT show more significant enhancement effect, improving the CPR by 74.14%, 72.91%, and 77.17%, respectively. The correlation analysis results suggest a negative linear correlation between the CPR and pore volume of the composites. The C-S-H gels and small capillary pores with a diameter below 50 nm are the significant factors determining the CPR of the composites. This illustrates that the CPR enhancement effects of various types of MWCNT change with the refinement of pore structure of UHPC. The enhancing mechanisms can be attributed to the nano-core effects of MWCNT, reducing the CH crystal size and primary cracks, inhibiting the growth and propagation of microcracks, refining the pore structure, optimizing the compactness of the cement paste matrix and interfacial transition zone, thus reducing the channels for chloride ion diffusion, while increasing the constrictivity and tortuosity of the channels.

Efficient Removal of Hazardous P-Nitroaniline from Wastewater by Using Surface-Activated and Modified Multiwalled Carbon Nanotubes with Mesostructure.

P-nitroaniline (PNA) is an aniline compound with high toxicity and can cause serious harm to aquatic animals and plants. Multiwalled carbon nanotubes (MWCNTs) are a multifunctional carbon-based material that can be applied in energy storage and biochemistry applications and semiconductors as well as for various environmental purposes. In the present study, MWCNTs (CO2-MWCNTs and KOH-MWCNTs) were obtained through CO2 and KOH activation. ACID-MWCNTs were obtained through surface treatment with an H2SO4-HNO3 mixture. Herein, we report, for the first time, the various MWCNTs that were employed as nanoadsorbents to remove PNA from aqueous solution. The MWCNTs had nanowire-like features and different tube lengths. The nanotubular structures were not destroyed after being activated. The KOH-MWCNTs, CO2-MWCNTs, and ACID-MWCNTs had surface areas of 487, 484, and 80 m2/g, respectively, and pore volumes of 1.432, 1.321, and 0.871 cm3/g, respectively. The activated MWCNTs contained C-O functional groups, which facilitate PNA adsorption. To determine the maximum adsorption capacity of the MWCNTs, the influences of several adsorption factors-contact time, solution pH, stirring speed, and amount of adsorbent-on PNA adsorption were investigated. The KOH-MWCNTs had the highest adsorption capacity, followed by the CO2-MWCNTs, pristine MWCNTs, and ACID-MWCNTs. The KOH-MWCNTs exhibited rapid PNA adsorption (>85% within the first 5 min) and high adsorption capacity (171.3 mg/g). Adsorption isotherms and kinetics models were employed to investigate the adsorption mechanism. The results of reutilization experiments revealed that the MWCNTs retained high adsorption capacity after five cycles. The surface-activated and modified MWCNTs synthesized in this study can effectively remove hazardous pollutants from wastewater and may have additional uses.

Synthesis of Zr-based metal-organic framework/MWCNTs composite for adsorption of enrofloxacin from aqueous solution

Enrofloxacin, as one of the specialized fluoroquinolone antibiotics, has become a typical “emerging” pollutant in aqueous environment because of its great stability and resistance to degradation. Therefore, it is important to find an effective method to remove it from aqueous solution. In order to check the presence of synergies between UiO-66 and MWCNTs on removal of enrofloxacin from aqueous solution, a composite material, known as UiO-66/MWCNTs, was synthesized by using hydrothermal method. The physical and chemical properties of the synthesized composite were characterized by using methods such as XRD, N2 adsorption–desorption, FT-IR, SEM and XPS. The results revealed that UiO-66/MWCNTs has large specific surface area (837.56 m2/g) and high porosity, as well as rich functional groups (C = C, –OH, –COOH). Factors such as contact time, initial concentration, temperature, pH, and ionic strength were considered to test the adsorption performance of pristine MWCNTs, pristine UiO-66 and UiO-66/MWCNTs composite for enrofloxacin. The results showed that the UiO-66/MWCNTs composite has a higher adsorption capacity at basic condition and the maximum adsorption capacities of enrofloxacin on composite was improved from 67.8 mg/g for MWCNTs and 92.8 mg/g for UiO-66 to 134.2 mg/g due to its higher adsorption active sites. The adsorption kinetics studies implied that the adsorption of enrofloxacin onto the studied sorbents involves in physio-chemical interactions and is an intra-particle diffusion controlling process. The isothermal experimental data were compatible with both Langmuir and Freundlich models, suggesting heterogeneous adsorption was the dominant during the course of adsorption. Additionally, the thermodynamic parameters indicated that the adsorption of enrofloxacin on UiO-66/MWCNTs was spontaneous and endothermic in nature. Finally, in combination with XPS analysis, the adsorption mechanism of enrofloxacin on UiO-66/MWCNTs was clarified to be the synergetic effect of chemical adsorption, hydrogen bond and π-π interaction. This work provides a new strategy for the removal of drugs from aqueous environment.

Functionalized Multiwalled Carbon Nanotubes for Highly Stable Room Temperature and Humidity-Tolerant Triethylamine Sensing.

Triethylamine (TEA) poses a significant threat to our health and is extremely difficult to detect at the parts-per-billion (ppb) level at room temperature. Carbon nanotubes (CNTs) are versatile materials used in chemiresistive vapor sensing. However, achieving high sensitivity and selectivity with a low detection limit remains a challenge for pristine CNTs, hindering their widespread commercial application. To address these issues, we propose functionalized multiwalled CNTs (MWCNTs) with carboxylic acid (COOH)-based sensing channels for ultrasensitive TEA detection under ambient conditions. Advanced structural analyses confirmed the necessary modification of MWCNTs after functionalization. The sensor exhibited excellent sensitivity to TEA in air, with a superior noise-free signal (10 ppb), an extremely low limit of detection (LOD ≈ 0.8 ppb), excellent repeatability, and long-term stability under ambient conditions. Moreover, the response values became more stable, demonstrating excellent humidity resistance (40-80% RH). Notably, the functionalized MWCNT sensor exhibited improved response and recovery kinetics (200 and 400 s) to 10 ppm of TEA compared to the pristine MWCNT sensor (400 and 1300 s), and the selectivity coefficient for TEA gas was improved by approximately three times against various interferants, including ammonia, formaldehyde, nitrogen dioxide, and carbon monoxide. The remarkable improvements in TEA detection were mainly associated with the large specific surface area, abundant active sites, adsorbed oxygen, and other defects. The sensing mechanism was thoroughly explained by using Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and gas chromatography-mass spectrometry (GC-MS). This study provides a new platform for CNT-based chemiresistive sensors with high selectivity, low detection limits, and enhanced precision with universal potential for applications in food safety and environmental monitoring.

Defect-Confinement Strategy for Constructing CuO Clusters on Carbon Nanotubes for Catalytic Oxidation of AsH3 at Room Temperature.

The efficient removal of the highly toxic arsine gas (AsH3) from industrial tail gases under mild conditions remains a formidable challenge. In this study, we utilized the confinement effect of defective carbon nanotubes to fabricate a CuO cluster catalyst (CuO/ACNT), which exhibited a capacity much higher than that of CuO supported on pristine multiwalled carbon nanotubes (MWCNT) (CuO/PCNT) for catalytically oxidizing AsH3 under ambient conditions. The experimental and theoretical results show that nitric acid steam treatment could induce MWCNT surface structural defects, which facilitated more stable anchoring of CuO and then improved the oxygen activation ability, therefore leading to excellent catalytic performance. Density functional theory (DFT) calculations revealed that the catalytic oxidation of AsH3 proceeded through stepwise dehydrogenation and subsequent recombination with oxygen to form As2O3 as the final product.

Room temperature detection of sulfur dioxide using functionalized carbon nanotubes

The construction of a simple sensor structure sensitive to sulfur dioxide (SO2) based on multi-walled carbon nanotubes (MWCNTs) functionalized by nitric acid is described in this study. The functionalized MWCNTs were comparatively analyzed by X-ray diffraction, Raman, and FTIR spectroscopy methods, and their morphology was observed by scanning electron microscope (SEM). The sensitivity to 5 ppm SO2 gas is based on the change of resistance of functionalized MWCNTs. Tests on the fabricated sensor were performed at room temperature and defined that functionalized MWCNTs are sensitive to SO2 gas compared with the pristine MWCNTs.

Effect of multi-walled carbon nanotubes on the visible light photocatalytic activity of AgInS2 for Rhodamine B degradation

Visible-light responsive AgInS2 (AIS) nanoparticles modified with either pristine multi-walled carbon nanotubes (p-MWCNTs) or mixed-acid (H2SO4 and HNO3) oxidized multi-walled carbon nanotubes (o-MWCNTs) were synthesized using a low-temperature liquid phase method. The resulting nanocomposites are denoted as p-MWCNTs/AIS or o-MWCNTs/AIS. The structure, morphology, and optical properties of the samples were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HRTEM), photoluminescence spectroscopy (PL), and ultraviolet-visible diffuse reflectance spectroscopy (UV–Vis DRS). The photocatalytic activity of p/o-MWCNTs/AIS towards the degradation of Rhodamine B (RhB) was investigated, and the optimal proportion of p/o-MWCNTs introduced on AIS was determined. A possible degradation mechanism of RhB over p/o-MWCNTs/AIS was proposed. The results demonstrated that p/o-MWCNTs were successfully incorporated into AIS, and the addition of an appropriate amount of p/o-MWCNTs improved the visible-light photocatalytic activity of AIS. Among the samples, 2 % o-MWCNTs/AIS exhibited the highest visible-light catalytic activity, achieving a degradation efficiency of 95 % within 40 min. The·⋅O2− species were identified as the main active species during the photocatalytic degradation process. The introduction of o-MWCNTs not only facilitated the separation of photogenerated electron-hole pairs (e−/h+) in AIS but also enhanced the visible-light absorption of AIS, leading to a significant improvement in its photocatalytic performance. Furthermore, the incorporation of o-MWCNTs greatly enhanced the cycling stability of AIS for reuse.

Antibiofilm Effect of Nitric Acid-Functionalized Carbon Nanotube-Based Surfaces against E. coli and S. aureus.

Chemically modified carbon nanotubes are recognized as effective materials for tackling bacterial infections. In this study, pristine multi-walled carbon nanotubes (p-MWCNTs) were functionalized with nitric acid (f-MWCNTs), followed by thermal treatment at 600 °C, and incorporated into a poly(dimethylsiloxane) (PDMS) matrix. The materials' textural properties were evaluated, and the roughness and morphology of MWCNT/PDMS composites were assessed using optical profilometry and scanning electron microscopy, respectively. The antibiofilm activity of MWCNT/PDMS surfaces was determined by quantifying culturable Escherichia coli and Staphylococcus aureus after 24 h of biofilm formation. Additionally, the antibacterial mechanisms of MWCNT materials were identified by flow cytometry, and the cytotoxicity of MWCNT/PDMS composites was tested against human kidney (HK-2) cells. The results revealed that the antimicrobial activity of MWCNTs incorporated into a PDMS matrix can be efficiently tailored through nitric acid functionalization, and it can be increased by up to 49% in the absence of surface carboxylic groups in f-MWCNT samples heated at 600 °C and the presence of redox activity of carbonyl groups. MWCNT materials changed the membrane permeability of both Gram-negative and Gram-positive bacteria, while they only induced the production of ROS in Gram-positive bacteria. Furthermore, the synthesized composites did not impact HK-2 cell viability, confirming the biocompatibility of MWCNT composites.

Surface functionalized multi-wall carbon nanotubes for degradation of organic dyes

Eliminating the hazardous dyes from the wastewater is essential for the sustainable furtherance of eco-friendly-oriented industrial growth. The untreated effluents containing dyes can damage the ecosystem and cause serious health issues to humans, animals, and aquatic species. In the present work, the multi-wall carbon nanotubes (MWCNTs) were functionalized using the combination of sulphuric acid and nitric acid. These functionalized multi-wall carbon nanotubes (F-MWCNTs) were characterized using Fourier transform infrared spectroscopy (FTIR) and energy dispersive X-ray analysis (EDAX) to confirm the presence of functional groups. The catalytic dye degradation efficiency of pristine multi-wall carbon nanotubes (P-MWCNTs) and F-MWCNTs was tested for methylene blue (MB), and indigo carmine (IC) dyes under dark and ultraviolet (UV) light exposure conditions. F-MWCNTs have exhibited appreciable degradation efficiency (∼90%) under dark and UV light compared to P-MWCNTs. An increment in efficiency was observed for UV-light-aided dye degradation. The impact of pH and temperature on degradation was analyzed in detail. The reaction kinetics was studied to determine the rate constants of the degradation reactions. A substantial quantum efficiency (QE) enhancement was noticed for F-MWCNTs compared to P-MWCNTs for both MB and IC degradation.