Heteroatom Doping in Pollutant Diesel Soot-Derived Nanocarbon for Enhanced Zn-Ion Storage Performance.

Herein, we have isolated onion-like nanocarbon (ONC) from the exhaust soot of diesel engines and further doped it with nitrogen (N) and sulfur (S) to fabricate N,S-co-doped ONC (N-S-ONC). To explore its application feasibility, we have assembled an aqueous Zn-ion hybrid supercapacitor (ZIHSC) with a N-S-ONC cathode, which attains high specific capacitance with good rate capability. In-depth analyses suggest that the mechanism of charge storage in the ONC is governed by both capacitive-controlled and diffusion-controlled processes, with the capacitive processes leading at all sweep rates. The ZIHSC demonstrated a good energy density of 50 Wh/kg, a maximum power density of 3.6 kW/kg, and an impressive cycle life with 73% capacitance retention after 50,000 charge-discharge cycles. The study suggests the potential possibly for the long-term application of BC derived nanocarbon in electrochemical energy storage systems (EESSs).

Nitrogen-doped carbon nano-onions/polypyrrole nanocomposite based low-cost flexible sensor for room temperature ammonia detection.

One of the frontier research areas in the field of gas sensing is high-performance room temperature-based novel sensing materials, and new family of low-cost and eco-friendly carbon nanomaterials with a unique structure has attracted significant attention. In this work, we propose a novel low-cost flexible room temperature ammonia gas sensor based on nitrogen-doped carbon nano-onions/polypyrrole (NCNO-PPy) composite material mounted low-cost membrane substrate was synthesized by combining hydrothermal and in-situ chemical polymerization methods. The proposed flexible sensor revealed high sensing performance when employed as the sensing material for ammonia detection at room temperature. The NCNO-PPy ammonia sensor exhibited 17.32% response for 100 ppm ammonia concentration with a low response time of 26 s. The NCNO-PPy based flexible sensor displays high selectivity, good repeatability, and long-term durability with 1 ppm as the lower detection limit. The proposed flexible sensor also demonstrated remarkable mechanical robustness under extreme bending conditions, i.e., up to 90° bending angle and 500 bending cycles. This enhanced sensing performance can be related to the potential bonding and synergistic interaction between nitrogen-doped CNOs and PPy, the formation of defects from nitrogen doping, and the presence of high reactive sites on the surface of NCNO-PPy composites. Additionally, the computational study was performed on optimized NCNO-PPy nanocomposite for both with and without NH3 interaction. A deeper understanding of the sensing phenomena was proposed by the computation of several electronic characteristics, such as band gap, electron affinity, and ionization potential, for the optimized composite.

Unveiling the Potential of Pt Nanoparticle-Decorated PEDOT:PSS Membranes for Efficient Gas Separation.

In the dynamic landscape of industrial processes, membrane technology offers a paradigm shift beyond energy-intensive separation techniques, exemplifying a progressive leap toward sustainability. In this regard, highly flexible and uniform poly(3,4-ethylenedioxythiophene)polystyrenesulfonate (PEDOT:PSS)-engineered membranes at a reduced thickness have been fabricated on track-etched poly(ethylene terephthalate) (PET) substrates. The membranes were functionalized and embedded with platinum nanoparticles (Pt NPs) having a higher affinity toward H2 gas. The materials and fabricated membranes were characterized by using high-resolution transmission electron microscopy (HRTEM) and field emission scanning electron microscopy (FESEM) techniques for morphological and structural analysis. FTIR and Raman characterizations were performed to study the characteristic bonds. The uniformity and quantification of Pt nanoparticle binding were tested through inductively coupled plasma mass spectrometry (ICP-MS) studies and FESEM with EDS mapping. The gas separation performance was studied using H2, N2, and CO2 gases in pure and mixed (H2/CO2 in 50:50) states. It was observed that the modified membrane showed a 116% increment in H2 permeability and 82 and 107% increment in H2/CO2 and H2/N2 selectivity values with pure gas, while a 121% increment in H2 permeability and 156% increment in H2/CO2 selectivity using mixed gas. The separation performance in pure and mixed gas states with repeated experiments conspicuously highlighted their prospective viability as prime contenders for gas separation applications.

ZIF-8 @polycarbonate nanocomposite membranes for improved permeability and selectivity for hydrogen gas.

Through this work, we are reporting high-performance ZIF-8 @polycarbonate nanocomposite membranes with satisfactory structural stability for improving the gas separation performance. ZIF-8 nanoparticles were synthesised using the wet chemical route with cubic morphology and controlled size using CTAB as a surfactant. The membranes were prepared using the solution casting method by adding ZIF-8 filler at various concentrations. The synthesised filler material and MMMs were characterised through X-ray diffraction spectroscopy (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and RAMAN spectroscopy techniques. The gas separation measurements were taken using H2, CO2, and N2 gas in the purest form. The SEM results confirm the formation of spherulite-like morphology with the addition of ZIF-8 due to the crystallisation of the polymer, which increased the membrane's free volume and opened up additional pathways for the transportation of the gas molecules. The gas separation results confirmed that the 15 wt% ZIF-8/PC nanocomposite membrane showed the maximum H2 permeability of 180,970 barrer with an increment of 316.03%, while H2/CO2 and H2/N2 selectivity showed the increments of 89.43% and 103.64%, respectively. Therefore, this PC/ZIF-8 system seems to be a promising approach to developing new H2 selective membranes with high gas permeability and gas selectivity values.

Crystal water intercalated interlayer expanded MoS2 nanosheets as a cathode for efficient zinc-ion storage.

Zinc-ion batteries (ZIBs) have attracted tremendous interest from the scientific community in recent years due to their extreme safety, cost-effectiveness, environmental benignity and the unique properties of the Zn anode. However, more suitable cathode materials are needed to achieve their potential widespread applications. MoS2, a 2D layered material with fascinating properties, could also serve as a cathode in ZIBs but is rarely studied due to its limited interlayer spacing, poor ionic/electronic conductivity and hydrophobicity. In this work, we report a facile hydrothermal method for synthesizing crystal water-intercalated MoS2 nanosheets and their application in efficient Zn-ion storage. Morphological characterization reveals the average thickness of the nanosheets to be 15.2 nm. With a large interlayer spacing (0.79 nm), high 1T content (49.7%) and high defects, MoS2·nH2O achieves a high discharge capacity of 197 mA h g-1 at 0.1 A g-1 in an aqueous 2 M ZnSO4 electrolyte. Moreover, it exhibits modest cyclic stability with 55% capacity retention after 1000 charge/discharge cycles. Furthermore, we evaluated the charge storage kinetics of crystal water-intercalated MoS2 nanosheets and realized that the electrochemical reaction is diffusion dominated with a diffusion coefficient of 10-10 to 10-13 cm2 s-1 in a 0.3 to 1.3 V potential window. This simple and cost-effective strategy for improving the performance of ZIBs by crystal water intercalation in 2D cathode materials will pave the way for their commercial-level grid-scale applications.

Energy-Dense Zinc Ion Hybrid Supercapacitors with S, N Dual-Doped Porous Carbon Nanocube Based Cathodes.

Zinc ion hybrid supercapacitors (ZIHSCs) are truly promising as next-generation high-performance energy storage systems because they could offer high energy density like batteries while exhibiting high power output and long cycle life traits of supercapacitors. The key point of constructing a high-performance ZIHSC is to couple the Zn anode with an appropriate cathode material, which has high theoretical capacity, cost-effectiveness, and intrinsic safety features. In this work, we have demonstrated the potentiality of S, N co-doped porous carbon nanocubes (S, N-CNCs) as a cathode material for devising a ZIHSC with excellent energy density and cycle life. The S, N-CNCs are prepared from a zeolitic imidazolate framework (ZIF)-8 precursor via a simultaneous pyrolyzing-doping strategy in an inert atmosphere. Resultant CNCs are monodisperse with an average size of around 65 nm and porous in nature, with uniform N and S doping throughout the structure. Benefitted from such hierarchical porous architecture and the presence of abundant heteroatoms, the assembled ZIHSC with S, N-CNC as the cathode and Zn-foil as the anode in a ZnSO4 aqueous electrolyte could reach a specific capacity as high as 165.5 mA h g-1 (331 F g-1) at 1 A g-1, which corresponds to a satisfactory energy density of 148.9 W h kg-1 at the power density of 900 W kg-1. The ZIHSC has displayed a good cycle stability with more than 70% capacity retention after 10,000 charge-discharge cycles. Furthermore, to verify the practical feasibility of such a cathode material, an aqueous 3D Zn@Cu//S, N-CNC full-cell device is fabricated, which has demonstrated a satisfactory specific capacity (49.6 mAh g-1 at 0.25 A g-1) and an impressive energy density (42.2 Wh kg-1 with 212.2 W kg-1). Full ZIHSC devices are also found to be efficient in powering light-emitting diodes, further substantiating their feasibility in next-generation energy storage applications.

Antibacterial and antibiofilm efficacy of green synthesized ZnO nanoparticles using Saraca asoca leaves.

Biofilms are made up of bacterial colonies and their extracellular polymeric substances (EPS) matrix, which protects the bacteria from adverse environmental conditions. The increasing drug resistivity of pathogenic bacteria is becoming an emergency for developing new antibacterial agents. In this study, we have synthesized the zinc oxide nanoparticles (ZnO NPs) using the leaf extract of Saraca asoca plant, and the antibacterial and antibiofilm activity of green synthesized ZnO NPs was measured against the biofilm-producing bacteria Bacillus subtilis. The disk diffusion data reveals that the zone of inhibition (ZOI) starts at a concentration of 0.5 mg/mL and minimum inhibition concentration (100 µg/mL) and minimum bactericidal concentration (150 µg/mL) values were also evaluated for green synthesized ZnO nanomaterials. Crystal violet test and microscopic examination were used to assess the impact of produced nanoparticles on biofilm development. The findings indicated a nearly 45%, 64%, and 83% suppression of biofilm development at 0.5 × MIC, 0.75 × MIC, and 1 × MIC value, respectively. The biofilm biomass of the preformed or matured biofilms by the ZnO NPs was evaluated to be 68%, 50%, and 33% at concentrations of 0.5 × MIC, 0.75 × MIC, and 1 × MIC which was concentration-dependent. Moreover, flow cytometry results suggest damage to the bacterial cell membrane. The data indicated that the proportion of dead cells increased with NP concentration in comparison to the control. Therefore, it can be concluded that the green synthetic ZnO nanoparticles showed excellent antibacterial and antibiofilm activity against the Bacillus subtilis bacteria that produce biofilms and that they could be a promising substitute agent for the treatment of biofilms and drug-resistant bacteria.

Sulphonated poly(ethersulfone)/carbon nano-onions-based nanocomposite membranes with high ion-conducting channels for salt removal via electrodialysis.

Herein, we are reporting the carbon nano onions (CNO)-based sulphonated poly(ethersulfone) (SPES) composite membranes by varying CNO content in SPES matrix for water desalination applications. CNOs were cost-effectively synthesized using flaxseed oil as a carbon source in an energy efficient flame pyrolysis process. The physico- and electrochemical properties of nanocomposite membranes were evaluated and compared to pristine SPES. Moreover, the chemical characterisation of composite membranes and CNOs were illustrated using techniques such as nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscope (FE-SEM), thermogravimetric analysis (TGA) and universal tensile machine (UTM). In the series of nanocomposite membranes, SPES-0.25 composite membrane displayed the highest water uptake (WU), ion exchange membrane (IEC) and ionic conductivity (IC) values that were enhanced by 9.25%, ~ 44.78% and ~ 6.10%, respectively, compared to pristine SPES membrane. The electrodialytic performance can be achieved maximum when membranes possess low power consumption (PC) and high energy efficiency (Ee). Therefore, the value of Ee and Pc for SPES-0.25 membrane has been determined to be 99.01 ± 0.97% and 0.92 ± 0.01 kWh kg-1, which are 1.12 and 1.11 times higher than the pristine SPES membrane. Hence, integrating CNO nanoparticles into the SPES matrix enhanced the ion-conducting channels.

Biomass-derived carbon nano-onions for the effective elimination of organic pollutants and oils from water.

Oil spillage and leakage of organic solvents have caused severe environmental and ecological damages. It is of great significance to develop a cost-efficient and green adsorbent material with high uptake efficiency to separate the oil-water mixture. In this work, biomass-derived CNOs were first time explored in the adsorption of organic pollutants and oils from water. Carbon nano-onions (CNOs) with hydrophobicity and oleophilicity were cost-effectively synthesized in an energy efficient flame pyrolysis process using flaxseed oil as a carbon source. The as-synthesized CNOs without any further surface modification have shown high adsorption efficiency in removing organic solvents and oils from the oil-water mixture. The CNOs could adsorb diverse organic solvents such as pyridine (36.81 mg g-1), dichloromethane (90.95 mg mg-1), aniline (76 mg mg-1), toluene (64 mg mg-1), chloroform (36.25 mg mg-1), methanol (49.25 mg mg-1), and ethanol (42.25 mg mg-1). The uptake capacity for petrol and diesel over CNOs was observed at 36.68 mg mg-1 and 58.1 mg mg-1, respectively. The adsorption of pyridine followed pseudo-second-order kinetics and Langmuir's isotherm model. Moreover, the adsorption efficiency of CNOs towards the remediation of pyridine was almost similar in real-water samples when tested in tap water, dam water, groundwater, and lake water. Similarly, the practical applicability for the separation of petrol and diesel was also verified in the real sample (sea water) and has been proven to be excellent. By simple evaporation, the recovered CNOs can be reused for more than 5 cycles. CNOs exhibit the promising potential to be used in practical applications for oil-polluted water treatment.

CO2 gas sensing properties of Na3BiO4-Bi2O3 mixed oxide nanostructures.

In this paper, we report Na3BiO4-Bi2O3 mixed oxide nanoplates for carbon dioxide gas sensing applications. These nanoplates have been synthesized using electrochemical deposition with potentiostatic mode on ITO substrate and characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD) to analyze their surface morphology and structure. SEM study shows the presence of horizontally aligned nanoplates stacked on top of one another (thickness ≈ 40 to 75 nm). XRD pattern shows the presence of monoclinic Na3BiO4 and Bi2O3. The gas percentage response is evaluated by measuring the change in electrical resistance of the nanoplates in the presence of carbon dioxide for different pressures at 50 °C, 75 °C, and 100 °C. Percentage response of more than 100% is seen at 30 psi gas pressure which increases to ≈ 277% at 90 psi at 100◦C.

Sustainable carbon nano-onions as an adsorbent for the efficient removal of oxo-anions.

The increasing threats of oxo-anions in drinking water have posed a serious threat to human health, aquatic environment, ecology, and sustainability. Accordingly, developments of cost-effective and sustainable nanomaterials for water remediation are on top priority and highly sought in global research community. Carbon nano-onions (CNOs) are one of the emerging nanomaterials for water purification because of its unique morphology, surface reactivity, high density of surface-active sites, and microporous structure. Herein, flaxseed oil-derived CNOs are utilized as efficient adsorbent for the removal of toxic oxo-anions. Aside from the green and economic nature, CNOs provide high adsorption efficiency ~ 806.45 mg g-1 for the removal of [Formula: see text] (99.9%) from aqueous system at ambient temperature, neutral pH in 70 min. The adsorption of [Formula: see text] onto CNOs was well fitted in pseudo-second order kinetics and followed the Langmuir adsorption isotherm model. The adsorption process was determined to be exothermic and spontaneous from the resulting thermodynamic characteristics. Furthermore, the high hydrophobic nature of CNOs make it recycling simpler. The real-life applicability of CNOs towards [Formula: see text] removal was tested in tap water, river water, and dam water. With all these observed results, CNOs show promise for practical water remediation applications.

Carbon Nano-Onion-Decorated ZnO Composite-Based Enzyme-Less Electrochemical Biosensing Approach for Glucose.

This study investigates the enzyme-less biosensing property of the zinc oxide/carbon nano-onion (ZnO/CNO) nanocomposite coated on a glassy carbon electrode. The ZnO/CNO nanocomposite was synthesized using the ex situ mixing method, and the structural characterization was done using XRD, SEM, and TEM, whereas functional groups and optical characterization were done through FTIR and UV-visible spectroscopy. The electrochemical sensing response of the ZnO/CNO nanocomposite for the linear range of glucose concentration (0.1-15 mM) was examined using cyclic voltammetry (CV) with a potential window of -1.6 to +1.6 V using 0.1 M NaOH as an electrolyte. The ZnO/CNO nanocomposites showed enhanced sensing ability toward glucose with a sensitive value of 606.64 µA/mM cm2. Amperometric i-t measurement supports the finding of CV measurement and showed good sensing ability of the electrode ZnO/CNO nanocomposite material for up to 40 days. The enhanced electrocatalytic activity of the ZnO/CNO nanocomposite is explained due to the synergetic effect of both ZnO and CNO. Our findings suggest a high potential for ZnO/CNO nanocomposite-based glucose biosensors, which could be further utilized to develop noninvasive skin-attached sensors for biomedical applications.

Charge storage mechanism in vanadium telluride/carbon nanobelts as electroactive material in an aqueous asymmetric supercapacitor.

A novel one-step method for fabricating vanadium telluride nanobelt composites for high-performance supercapacitor applications is reported. The nanobelts are realized by direct tellurization of vanadium oxide in-situ formed via decomposition of ammonium metavanadate in argon atmosphere. Use of melamine as precursor helps in forming graphitic carbon layers during pyrolization on which the nanobelts are grafted. Morphological analysis suggests interconnected nanobelts of ∼23.0 nm width coming out of carbon structure. As pseudocapacitive electrode, vanadium telluride/carbon (C) composite exhibits interesting electrochemical performance within a potential window of 0-1.0 V in 1.0 M sodium sulfate electrolyte along with excellent capacitance retention during 5000 cycles. In-depth analysis suggests that the charge storage mechanism in the composite is governed by both diffusion-controlled and diffusion-independent processes with the former dominating at slower scan rates and later at faster scan rates. The asymmetric supercapacitor assembled using vanadium telluride/C and activated charcoal (AC) as respective positive and negative electrodes exhibited an energy/power combination of 19.3 Wh/kg and 1.8 kW/kg within a potential window of 0-1.8 V in aqueous electrolyte. This strategy to improve capacitance along with potential window in an aqueous electrolyte would facilitate development of high-performance energy storage devices with metal chalcogenides.

Metal-Immobilized Micellar Aggregates of a Block Copolymer from a Mixed Solvent for a SERS-Active Sensing Substrate and Versatile Dip Catalysis.

Here, we have reported micellar aggregations of an amphiphilic block copolymer in mixed solvent and their subsequent use as a template for the fabrication of a very dense, tunable metal nanoparticle-decorated surface for SERS and flexible dip catalysis applications. A silver nanoparticle-immobilized layer on silicon substrates shows excellent SERS (surface-enhanced Raman scattering)-based sensing performance for model analyte rhodamine B up to 10-6 M concentration with a well-defined calibration curve. Furthermore, a facile approach to the preparation of metal NP-immobilized BCP membranes as efficient dip catalyst for two model reactions (the reduction of nitrophenol and the Suzuki-Miyaura reaction of iodobenzene or 2,7-diiodofluorene with phenyl boronic acid) is also demonstrated. The Ag NP-decorated film exhibits high efficiency and extensive reusability in a prototype reaction such as the reduction of nitrophenol by sodium borohydride with a very high turnover number, >126 (for a single use), whereas the Pd NP-immobilized film also has a high, ∼100%, reaction yield and extensive reusability and applicable for different aromatic systems. This work provides a new platform for the design and synthesis of a functionalizable, flexible, and highly mechanically stable dip catalyst which is highly demanded in the catalytic production of value-added chemicals and environmental applications such as wastewater treatment.

UV-irradiation assisted functionalization and binding of Pd nanoparticles in polycarbonate membranes for hydrogen separation.

For hydrogen-based energy systems development, purified hydrogen (H2) is a basic requirement and it can be achieved by using the H2-selective membranes. For having H2-selective membranes, it is a decent approach to embed the H2-sensitive materials in the polymeric membranes. Palladium (Pd) is one of the widely used materials for hydrogen-selective membranes due to its strong affinity towards H2 absorption. In the present work, we have used Pd nanoparticles in UV-functionalized track-etched polycarbonate (PC) membranes for better selectivity and permeability of H2 gas. In the UV-irradiation process of membranes, the photo-fries mechanism leads to the C-O bond breaking from the carbonate group of PC molecules and as a result, there is a high number of bond breaking. This phenomenon provides the more active sites for the attachment of Pd nanoparticles in comparison with the pristine PC membrane. The gas permeability of these membranes suggests that the selectivity of H2 over nitrogen (N2) and carbon dioxide (CO2) is increased by the addition of uniformly distributed Pd nanoparticles in the functionalized membranes.

Dose dependent enhanced antibacterial effects and reduced biofilm activity against Bacillus subtilis in presence of ZnO nanoparticles.

Bacterial biofilms are self-produced matrix of sticky extracellular polymeric substances. They result in fouling in the food industry, water treatment plants, and possess significant environmental and industrial impacts. Nanoparticles have shown immense potential and have been effective in combating bacterial biofilm, which is the common cause of drug resistance development, biofouling in water treatment plants and the food industry. Hence, in order to explore the same, Zinc oxide nanoparticles have been synthesized by chemical synthesis method and their action against Bacillus subtilis biofilm formation was evaluated in this study by crystal violet and ROS assay. The dose-dependent reduction in biofilm biomass and density was observed as a result of nanoparticle exposure. There was considerable reduction in biofilm formation after treatment with ZnO nanoparticles. Change in surface morphology of the Bacillus subtilis cells was observed which could be due to oxidative stress induced by ZnO nanoparticles. The oxidative stress was estimated by measurement of catalase activity that also showed dose-dependent decrease.

Flower-like Bi2S3 nanostructures as highly efficient anodes for all-solid-state lithium-ion batteries.

Herein, we introduce the detailed electrochemical reaction mechanism of Bi2S3 (bulk as well as nanostructure) as a highly efficient anode material with Li-ions in an all-solid-state Li-ion battery (LIB). Flower-like Bi2S3 nanostructures were synthesized by a hydrothermal method and were used as an anode material in a LIB with LiBH4 as a solid electrolyte. The X-ray diffraction (XRD) pattern verified the formation of Bi2S3 nanostructures, which belongs to the orthorhombic crystal system (JCPDS no. 00-006-0333) with the Pbnm space group. Morphological studies confirmed the flower-like structure of the obtained product assembled from nanorods with the length and diameter in the range of 150-400 nm and 10-150 nm respectively. The electrochemical galvanostatic charge-discharge profile of these nanostructures demonstrates exciting results with a high discharge and charge capacity of 685 mA h g-1 & 494 mA h g-1 respectively at 125 °C. The discharge and charge capacities were observed as 375 mA h g-1 and 352 mA h g-1 after 50 cycles (with 94% coulombic efficiency), which are much better than the cells having bulk Bi2S3 as the anode material.

An efficient and environmentally sustainable domino protocol for the synthesis of structurally diverse spiroannulated pyrimidophenazines using erbium doped TiO2 nanoparticles as a recyclable and reusable heterogeneous acid catalyst.

An efficient and environmentally sustainable domino protocol has been presented for the synthesis of structurally diverse spiroannulated pyrimidophenazines involving a four component reaction of 2-hydroxynaphthalene-1,4-dione, benzene-1,2-diamine, cyclic ketones and amino derivatives in the presence of erbium doped TiO2 nanoparticles as a recyclable and reusable heterogeneous acid catalyst. The present synthetic protocol features mild reaction conditions with operational simplicity, excellent yield with high purity, short reaction time and high atom economy with the use of a recoverable and reusable environmentally sustainable heterogeneous catalyst.

Multi walled carbon nano tubes induced hepatotoxicity in Swiss albino mice.

In the present study, multi walled carbon nano tubes (MWCNTs) were synthesized using chemical vapour deposition (CVD) technique. Swiss albino mice were orally administered with single dose of 60 and 100 mg/kg body weight of purified and functionalized MWCNTs suspended in water. The mice were autopsied on 7, 14, 21 and 28 days post exposure. Liver was taken out and part of it fixed in Bouin's solution for histopathological examinations. The remaining part was immersed in cold saline, blotted dry, weighed quickly and homogenized in ice cold buffer. The activity of superoxide dismutase (SOD) and catalase (CAT) was immediately measured in the supernatant. The MWCNTs in liver led to pathological changes, including injury to macrophages, cellular swelling, unspecific inflammation, spot necrosis and blood coagulation. Estimation of SOD and CAT showed altered levels in the experimental groups as compared to controls. Therefore, MWCNTs from manufactured and combustion sources in the environment can have adverse effects on human health.

Enhancement of hydrogen gas permeability in electrically aligned MWCNT-PMMA composite membranes.

The multi-walled carbon nanotube (MWCNT) dispersed polymethylmethacrylate (PMMA) composite membranes have been prepared for hydrogen gas permeation application. Composite membranes are characterized by Raman spectroscopy, optical microscopy, X-ray diffraction, electrical measurements and gas permeability measurements. The effect of electric field alignment of MWCNT in PMMA matrix on gas permeation has been studied for hydrogen gas. The permeability measurements indicated that the electrically aligned MWCNT in PMMA has shown almost 2 times higher permeability for hydrogen gas as compare to randomly dispersed MWCNT in PMMA. The enhancement in permeability is explained on the basis of well aligned easy channel provided by MWCNT in electrically aligned sample. The effect of thickness of membrane on the gas permeability also studied and thickness of about 30microm found to be optimum thickness for fast hydrogen gas permeates.