Synthesis of carbon nanotubes using pre-sintered oil fly ash via a reproducible process with large-scale potential.

Oil fly ash (OFA) is a byproduct generated by the burning of heavy crude oil in factories and power plants. Millions of tons of OFA is produced annually worldwide and is mostly treated as solid waste. Extensive efforts have been made to utilize OFA and reduce its environmental effects. Recently, OFA has been found to be a suitable catalyst and co-precursor for carbon nanotube (CNTs) production. However, the treatment methods used are expensive and time consuming. Here, we describe a new method for OFA treatment and provide optimized growth conditions for CNTs production. Pre-sintering of OFA at elevated temperatures (400-450 °C) in air or vacuum using a chemical vapor deposition (CVD) tube furnace (80-100 min) is a very effective treatment method for CNTs growth under optimum growth conditions. The optimum parameters for CNTs growth were growth temperature, gas pressure, gas flow rate, and growth time. Well-defined, thin nanotubes with diameters of 20-40 nm were produced. Bamboo-like nanotubes with zigzag curved walls were also observed in the produced CNTs. The weight percentage of the produced CNTs was approximately twice that of the treated OFA. Consequently, the pre-sintering method exhibited suitability for the mass production of CNTs. Thus, large quantities of the nanomaterial can be supplied for use in various applications, e.g., polymer composites, the rubber industry, construction materials, and lubricant additives.

Size controlled ultrafine CeO2 nanoparticles produced by the microwave assisted route and their antimicrobial activity.

Cerium oxide (CeO2) nanoparticles (NPs) have a wide range of biological and biomedical applications. This work describes a new methodology for producing ultrafine, highly uniform NPs with controlled sizes using the chemical microwave assisted route. The size of CeO2-NPs decreased from 10 to 5 nm by increasing the molar ratio of cerium nitrate Ce(NO3)3.(6H2O) to that of hexamethylenetetramine (C6H12N) from 1:20 to 20:20. Detailed information about their structural characterization was obtained from the XRD, UV-visible, photoluminescence, Raman spectroscopy, SEM, TEM and AFM. These CeO2-NPs were tested as antimicrobial agent against Gram-negative (Escherichia.coli), Gram-positive (Bacillus.subtilis) bacteria and yeast (Saccharomyces cerevisiae). The obtained results showed significant inhibition of these strain even at low concentration of CeO2-NPs. The CeO2-NPs with the molar ratio 5:20 had the most effective inhibition against E.coli (~70%) at a concentration of 20 µL. The CeO2-NPs with the ratio 12:20 were found to be the most effective against B.subtilis (inhibition ~68%). On the other hand, CeO2-NPs synthesized with the 20:20 molar ratio caused the highest inhibition for S. cerevisiae (~60%). It is observed that at higher NPs concentration (i.e., >20 µL) the inhibition of these strains decreased. The antimicrobial activity may be attributed to the penetrating power of CeO2-NPs size beside the generated oxygen species radicals that caused inhibition of bacterial growth.

Enhanced UV upconversion emission using plasmonic nanocavities.

Upconversion of near infrared (NIR) into ultraviolet (UV) radiation could lead to a number of applications in bio-imaging, diagnostics and drug delivery. However, for bare nanoparticles, the conversion efficiency is extremely low. In this work, we experimentally demonstrate strongly enhanced upconversion emission from an ensemble of ß-NaYF4:Gd3+/Yb3+/Tm3+ @NaLuF4 core-shell nanoparticles trapped in judiciously designed plasmonic nanocavities. In doing so, different metal platforms and nanostructures are systematically investigated. Our results indicate that using a cross-shape silver nanocavity, a record high enhancement of 170-fold can be obtained in the UV band centered at a wavelength of 345 nm. The observed upconversion efficiency improvement may be attributed to the increased absorption at NIR, the tailored photonic local density of states, and the light out-coupling characteristics of the cavity.

Carbon dioxide-activated mesoporous date palm fronds carbon integrated with MnO2/polyaniline for highly efficient capacitive deionization of water.

The continuous population growth and drying up the freshwater reservoirs around the world are increasing the demand for fresh water. Therefore, there is an urgent need to explore newer technologies able to purify water on large scales for human usage. Capacitive deionization is one of the most promising approaches to generate fresh water by the removal of salt ions from brackish water. In this work, we prepared three different capacitive deionization electrodes using carbonized palm tree fronds (PFC). These PFC activation was achieved using CO2 at 900°C. To generate the deionization electrodes, PFC activated carbon was combined with either polyaniline (PANI), MnO2, or both (PFC-PANI, PFC-MnO2, and PFC-MnO2-PANI). The MnO2 and PANI provided additional functionality and enhanced electrical conductivity, which resulted in much higher Na+ and Cl- ions adsorption. The BET surface area of PFC-MnO2-PANI was estimated to be 208.56 m2/g, which is approximately three times that of PCF-PANI and PFC-MnO2 alone. The morphological analysis showed that the PANI and MnO2 nanorods were well dispersed throughout the PFC network. Although PANI and MnO2 is largely embedded inside the PFC network, some remnants are visible on the surface of the electrodes. The cyclic voltammetry (CV) curves showed capacitive behavior of all electrodes in which PFC-MnO2-PANI showed highest specific capacitance of 84 F/g, while the PFC-MnO2 and PFC-PANI showed 42 and 43 F/g, respectively. Owing to its enhanced functionality and CV characteristics, the PFC-MnO2-PANI showed maximum salt adsorption capacity of 10.5 mg/g in contrast to 3.72 and 5.64 mg/g for PFC-MnO2 and PFC-PANI, respectively. Moreover, the measured contact angle for PFC-MnO2-PANI was ~51°, which indicates the hydrophilic nature of electrode that improved ions adsorption. PRACTITIONER POINTS: Date tree fronds were converted into mesopores carbon using CO2 as activation agent. Three composites were prepared with PANI, MnO2, and date palm fronds activated carbon (PFC-MnO2, PFC-MnO2-PANI, and PFC-PANI). Surface area, pore profile, surface morphology, electrochemical behavior, desalination performance, and hydrophilicity of all the electrodes were investigated. The PFC-MnO2-PANI showed maximum salt adsorption capacity of 10.5 mg/g in contrast to 3.72 and 5.64 mg/g for PFC-MnO2 and PFC-PANI, respectively.

Highly Uniform Nanodiamond-Graphene Composites Microspheres for Electrocatalytic Hydrogen Evolution.

To progress the clean hydrogen-gas-based energy economy, there is a demand for cost-effective, highly efficient catalysts to facilitate the hydrogen evolution reaction process (HER). Due to the amazing catalytic capabilities of two-dimensional materials, extensive research has been done on these structures. However, most of the described syntheses take a lot of time, are challenging, and are ineffective. The present work demonstrates the performance of the recently reported nanodiamond/graphene composite microsphere ND-GCSs as a catalyst for HER. These spheres were produced via the microwave-irradiation approach. A modified process was adopted to improve the particle size uniformity and yield. The prepared composite spheres showed very interesting catalytic activity for the HER when assembled on a screen-printed carbon electrode. The prepared ND-GCSs@SPCE showed a significant shift of the onset potential to ca. -450 mV and a small Tafel slope value of ca. 85 mV/decade. The electron transfer was drastically enhanced with a tremendous decrease in charge transfer resistance to ca. 265 Ω. The electrocatalyst showed excellent long-term stability for the HER application. Additionally, this novel composite structure might be beneficial for diverse applications including batteries, supercapacitors, catalyst supports, and more.

Resulting Effect of the p-Type of ZnTe: Cu Thin Films of the Intermediate Layer in Heterojunction Solar Cells: Structural, Optical, and Electrical Characteristics.

The microstructural, electrical, and optical properties of Cu-doped and undoped ZnTe thin films grown on glass substrates are covered in this article. To determine the chemical makeup of these materials, both energy-dispersive X-ray (EDAX) spectroscopy and X-ray photoelectron spectroscopy were employed. The cubic zinc-blende crystal structure of ZnTe and Cu-doped ZnTe films was discovered using X-ray diffraction crystallography. According to these microstructural studies, the average crystallite size increased as the amount of Cu doping increased, whereas the microstrain decreased as the crystallinity increased; hence, defects were minimized. The Swanepoel method was used to compute the refractive index, and it was found that the refractive index rises as the Cu doping levels rises. The optical band gap energy was observed to decrease from 2.225 eV to 1.941 eV as the Cu content rose from 0% to 8%, and then slightly increase to 1.965 eV at a Cu concentration of 10%. The Burstein-Moss effect may be connected to this observation. The larger grain size, which lessens the dispersion of the grain boundary, was thought to be the cause of the observed increase in the dc electrical conductivity with an increase in Cu doping. In structured undoped and Cu-doped ZnTe films, there were two carrier transport conduction mechanisms that could be seen. According to the Hall Effect measurements, all the grown films exhibited a p-type conduction behavior. In addition, the findings demonstrated that as the Cu doping level rises, the carrier concentration and the Hall mobility similarly rise, reaching an ideal Cu concentration of 8 at.%, which is due to the fact that the grain size decreases grain boundary scattering. Furthermore, we examined the impact of the ZnTe and ZnTe:Cu (at Cu 8 at.%) layers on the efficiency of the CdS/CdTe solar cells.

Thermoelectric and power generation of 2D structured pieces of graphene-nanodiamonds nanocomposite.

Recently, the ultrafine 2D structured nanocomposite of graphene (Gr)-nanodiamonds (NDs) produced by a microwave-assisted chemical route was found to have attractive structural properties. This new 2D structured nanocomposite may be employed for a wide spectrum of applications including thermoelectricity (TE) applications. It is well established that TE materials should be highly effective to be used for designing operative devices for powering or cooling small devices. To fulfill such an objective, the functional TE material should possess a high-power factor and low thermal conductivity. In this study, NDs were successfully integrated into Gr with a magnificent structural alteration to the Gr layers/sheets. This structural modification was found to impact the TE final outcome above and below room temperature (RT). The obtained results showed that at 215 K the power factor value was increased from 4 µW m-1 K-2 for the pure Gr to ∼20 µW m-1 K-2 for the Gr-NDs nanocomposite. At higher T, e.g. 365 K, these values slightly decreased, but with clear superiority for the Gr-NDs nanocomposite. The thermal conductivity of the Gr-NDs nanocomposite was significantly reduced to ∼12% of that of the pure Gr, which could reflect a significant enhancement in the value of the figure of merit by >45 times. Furthermore, the output power generated by a single small leg module made of the Gr-NDs nanocomposite was measured and found to be measurable. The obtained values are still relatively low for practical application, but this newly produced material has great potential to be further developed for TE applications.

Thermoelectric Power Generation of TiS2/Organic Hybrid Superlattices Below Room Temperature.

Recently, the n-type TiS2/organic hybrid superlattice (TOS) was found to have efficient thermoelectric (TE) properties above and near room temperature (RT). However, its TE performance and power generation at the temperature gradient below RT have not yet been reported. In this work, the TE performance and power generation of the TOS above and below RT were investigated. The electrical conductivity (σ) and Seebeck coefficient (S) were recorded as a function of temperature within the range 233-323 K. The generated power at temperature gradients above (at ΔT = 20 and 40 K) and below (at ΔT = -20 and -40 K) RT was measured. The recorded σ decreased by heating the TOS, while |S| increased. The resulting power factor recorded ~100 µW/mK2 at T = 233 K with a slight increase following heating. The charge carrier density and Hall mobility of the TOS showed opposite trends. The first factor significantly decreased after heating, while the second one increased. The TE-generated power of a single small module made of the TOS at ΔT = 20 and 40 K recorded 10 and 45 nW, respectively. Surprisingly, the generated power below RT is several times higher than that generated above RT. It reached 140 and 350 nW at ΔT = -20 and -40 K, respectively. These remarkable results indicate that TOS might be appropriate for generating TE power in cold environments below RT. Similar TE performances were recorded from both TOS films deposited on solid glass and flexible polymer, indicating TOS pertinence for flexible TE devices.

Epoxy Flooring/Oil Fly Ash as a Multifunctional Composite with Enhanced Mechanical Performance for Neutron Shielding and Chemical-Resistance Applications.

Heavy-oil fly ash (HOFA) is a graphitic carbon powder extracted in vast amounts as a waste material from burning crude oil in power plants. This HOFA has attractive structural properties besides its high amount of pure carbon (∼90 wt %). This powder exists in spherical, highly porous micron-sized particles, which implies its great potential as a mechanical reinforcement for different polymers. In this work, HOFA has been utilized to enhance the mechanical properties of epoxy flooring at HOFA weight fractions of 0, 1, 1.6, and 3.2 wt %. The obtained results revealed that the prepared epoxy-flooring/HOFA composites at a HOFA content of 1.6 wt % showed significant mechanical improvements compared with the pristine polymer. The tensile strength and Young's module values were enhanced by ∼17 and 11%, respectively. Furthermore, the neutron-shielding performance was investigated. The composite with 1.6 wt % showed better neutron attenuation and lower transmittance than the pristine epoxy. The chemical resistance was also extensively studied against sodium hydroxide, nitric acid, and sulfuric acid. The changes in morphology, chemical elements, mass, volume, and molecular structures were investigated rigorously for pristine epoxy and its composite with HOFA at 1.6 wt %. After exposure to these chemicals for 21 days, the tested properties of the epoxy-flooring/HOFA composite showed better chemical resistance than that of the pristine epoxy. Where the epoxy-flooring/HOFA composite showed a surface with low cracks and blistering, it showed lesser changes in mass and volume and fewer molecular structure changes. These results indicated that it is possible to use this multifunctional composite for several applications, including the petrochemical industry, radiation shielding, construction, and automobiles.

Superparamagnetic Multifunctionalized Chitosan Nanohybrids for Efficient Copper Adsorption: Comparative Performance, Stability, and Mechanism Insights.

To limit the dangers posed by Cu(II) pollution, chitosan-nanohybrid derivatives were developed for selective and rapid copper adsorption. A magnetic chitosan nanohybrid (r-MCS) was obtained via the co-precipitation nucleation of ferroferric oxide (Fe3O4) co-stabilized within chitosan, followed by further multifunctionalization with amine (diethylenetriamine) and amino acid moieties (alanine, cysteine, and serine types) to give the TA-type, A-type, C-type, and S-type, respectively. The physiochemical characteristics of the as-prepared adsorbents were thoroughly elucidated. The superparamagnetic Fe3O4 nanoparticles were mono-dispersed spherical shapes with typical sizes (~8.5-14.7 nm). The adsorption properties toward Cu(II) were compared, and the interaction behaviors were explained with XPS and FTIR analysis. The saturation adsorption capacities (in mmol.Cu.g-1) have the following order: TA-type (3.29) > C-type (1.92) > S-type (1.75) > A-type(1.70) > r-MCS (0.99) at optimal pH0 5.0. The adsorption was endothermic with fast kinetics (except TA-type was exothermic). Langmuir and pseudo-second-order equations fit well with the experimental data. The nanohybrids exhibit selective adsorption for Cu(II) from multicomponent solutions. These adsorbents show high durability over multiple cycles with desorption efficiency > 93% over six cycles using acidified thiourea. Ultimately, QSAR tools (quantitative structure-activity relationships) were employed to examine the relationship between essential metal properties and adsorbent sensitivities. Moreover, the adsorption process was described quantitatively, using a novel three-dimensional (3D) nonlinear mathematical model.

Freestanding Activated Carbon Nanocomposite Electrodes for Capacitive Deionization of Water.

Freshwater reserves are being polluted every day due to the industrial revolution. Man-made activities have adverse effects upon the ecosystem. It is thus the hour of need to explore newer technologies to save and purify water for the growing human population. Capacitive deionization (CDI) is being considered as an emerging technique for removal of excess ions to produce potable water including desalination. Herein, cost-effective activated carbon incorporated with carbon nanotubes (CNT) was used as a freestanding electrode. Further, the desalination efficiency of the designed electrodes was tuned by varying binder concentration, i.e., polyvinylidene difluoride (PVDF) in the activated carbon powder and CNT mixture. PVDF concentration of 5, 7.5, 10, and 12.5 wt% was selected to optimize the freestanding electrode formation and further applied for desalination of water. PVDF content affected the surface morphology, specific surface area, and functional groups of the freestanding electrodes. Moreover, the electrical conductivity and specific surface area changed with PVDF concentration, which ultimately affected the desalination capacity using the freestanding electrodes. This study paves the way to produce cost effective carbon-based freestanding electrodes for capacitive deionization and other applications including battery electrodes.

Electrochemical Performance and Hydrogen Storage of Ni-Pd-P-B Glassy Alloy.

The search for hydrogen storage materials is a challenging task. In this work, we tried to test metallic glass-based pseudocapacitive material for electrochemical hydrogen storage potential. An alloy ingot with an atomic composition of Ni60Pd20P16B4 was prepared via arc melting of extremely pure elements in an Ar environment. A ribbon sample with a width of 2 mm and a thickness of 20 mm was produced via melt spinning of the prepared ingot. Electrochemical dealloying of the ribbon sample was conducted in 1 M H2SO4 to prepare a nanoporous glassy alloy. The Brunauer-Emmett-Teller (BET) and Langmuir methods were implemented to obtain the total surface area of the nanoporous glassy alloy ribbon. The obtained values were 6.486 m2/g and 15.082 m2/g, respectively. The Dubinin-Astakhov (DA) method was used to calculate pore radius and pore volume; those values were 1.07 nm and 0.09 cm3/g, respectively. Cyclic voltammetry of the dealloyed samples revealed the pseudocapacitive nature of this alloy. Impedance of the dealloying sample was measured at different frequencies through use of electrochemical impedance spectroscopy (EIS). A Cole-Cole plot established a semicircle with a radius of ~6 Ω at higher frequency, indicating low interfacial charge-transfer resistance, and an almost vertical Warburg slope at lower frequency, indicating fast diffusion of ions to the electrode surface. Charge-discharge experiments were performed at different constant currents (75, 100, 125, 150, and 200 mA/g) under a cutoff potential of 2.25 V vs. Ag/AgCl electrode in a 1 M KOH solution. The calculated maximum storage capacity was 950 mAh/g. High-rate dischargeability (HRD) and capacity retention (Sn) for the dealloyed glassy alloy ribbon sample were evaluated. The calculated capacity retention rate at the 40th cycle was 97%, which reveals high stability.

Mesoporous Magnetic Cysteine Functionalized Chitosan Nanocomposite for Selective Uranyl Ions Sorption: Experimental, Structural Characterization, and Mechanistic Studies.

Nuclear power facilities are being expanded to satisfy expanding worldwide energy demand. Thus, uranium recovery from secondary resources has become a hot topic in terms of environmental protection and nuclear fuel conservation. Herein, a mesoporous biosorbent of a hybrid magnetic-chitosan nanocomposite functionalized with cysteine (Cys) was synthesized via subsequent heterogeneous nucleation for selectively enhanced uranyl ion (UO22+) sorption. Various analytical tools were used to confirm the mesoporous nanocomposite structural characteristics and confirm the synthetic route. The characteristics of the synthesized nanocomposite were as follows: superparamagnetic with saturation magnetization (MS: 25.81 emu/g), a specific surface area (SBET: 42.56 m2/g) with a unipore mesoporous structure, an amine content of ~2.43 mmol N/g, and a density of ~17.19/nm2. The experimental results showed that the sorption was highly efficient: for the isotherm fitted by the Langmuir equation, the maximum capacity was about 0.575 mmol U/g at pH range 3.5-5.0, and Temperature (25 ± 1 °C); further, there was excellent selectivity for UO22+, likely due to the chemical valent difference. The sorption process was fast (~50 min), simulated with the pseudo-second-order equation, and the sorption half-time (t1/2) was 3.86 min. The sophisticated spectroscopic studies (FTIR and XPS) revealed that the sorption mechanism was linked to complexation and ion exchange by interaction with S/N/O multiple functional groups. The sorption was exothermic, spontaneous, and governed by entropy change. Desorption and regeneration were carried out using an acidified urea solution (0.25 M) that was recycled for a minimum of six cycles, resulting in a sorption and desorption efficiency of over 91%. The as-synthesized nanocomposite's high stability, durability, and chemical resistivity were confirmed over multiple cycles using FTIR and leachability. Finally, the sorbent was efficiently tested for selective uranium sorption from multicomponent acidic simulated nuclear solution. Owing to such excellent performance, the Cys nanocomposite is greatly promising in the uranium recovery field.

Structural, morphological, and optical properties of carbon nanoparticles unsheathed from date palm fronds.

Several studies have reported the synthesis of carbon nanoparticles (CNPs) by various methods. In this study, an easy one-step process to unsheathe CNPs from date palm fronds through a top-down ball milling method has been reported. The CNPs were characterized using various spectroscopic and microscopic methods to determine their structural and morphological features, optical properties, crystallinity, physicochemical properties, and particle stability. Transmission electron microscopy (TEM) revealed that the obtained CNPs' size ranged from 4 to 22 nm in a crystalline form. Scanning electron microscopy (SEM) confirmed their spherical shape, while the maximum photoluminescence (PL) intensity was recorded at 464 nm when excited at 375 nm. The unsheathed CNPs produced a good quantum yield (QY) of 3.24%. Furthermore, the CNPs exhibited high Raman ratios of I D/I G and I 2D/I G with values of 0.59 and 0.04, respectively, verifying their multilayer crystalline graphitic nature. These Raman ratios also agree with the X-ray diffractometry (XRD) results. The CNPs' sp2 and sp3 carbon bonds were confirmed by X-ray photoelectron spectroscopy (XPS), with oxygen on the surface forming carboxyl and carbonyl groups with no other observable impurities. Furthermore, the extracted CNPs showed excellent PL properties for up- and down-conversion. These properties are exemplary for low-cost biomass with potential applications in biomedicine. Therefore, the extracted CNPs reported in this study have potential applications in optical imaging.

Carbon Nanoparticles Extracted from Date Palm Fronds for Fluorescence Bioimaging: In Vitro Study.

Numerous studies have been reported on single- and multicolored highly fluorescent carbon nanoparticles (FCNPs) originating from various sources and their potential applications in bioimaging. Herein, multicolored biocompatible carbon nanoparticles (CNPs) unsheathed from date palm fronds were studied. The extracted CNPs were characterized via several microscopic and spectroscopic techniques. The results revealed that the CNPs were crystalline graphitic and hydrophilic in nature with sizes ranging from 4 to 20 nm. The unsheathed CNPs showed exemplary photoluminescent (PL) properties. They also emitted bright blue colors when exposed to ultraviolet (UV) light. Furthermore, in vitro cellular uptake and cell viability in the presence of CNPs were also investigated. The cell viability of human colon cancer (HCT-116) and breast adenocarcinoma (MCF-7) cell lines with aqueous CNPs at different concentrations was assessed by a cell metabolic activity assay (MTT) for 24 and 48 h incubations. The results were combined to generate dose-response curves for the CNPs and evaluate the severity of their toxicity. The CNPs showed adequate fluorescence with high cell viability for in vitro cell imaging. Under the laser-scanning confocal microscope, the CNPs with HCT-116 and MCF-7 cell lines showed multicolor fluorescence emissions, including blue, green, and red colors when excited at 405, 458, and 561 nm, respectively. These results prove that unsheathed CNPs from date palm fronds can be used in diverse biomedical applications because of their low cytotoxicity, adequate fluorescence, eco-friendly nature, and cheap production.

High Thermoelectric Power Generation by SWCNT/PPy Core Shell Nanocomposites.

Polypyrrole (PPy) is a conducting polymer with attractive thermoelectric (TE) properties. It is simple to fabricate and modify its morphology for enhanced electrical conductivity. However, such improvement is still limited to considerably enhancing TE performance. In this case, a single-wall carbon nanotube (SWCNT), which has ultrathin diameters and exhibits semi-metallic electrical conductivity, might be a proper candidate to be combined with PPy as a core shell one-dimensional (1D) nanocomposite for higher TE power generation. In this work, core shell nanocomposites based on SWCNT/PPy were fabricated. Various amounts of pyrrole (Py), which are monomer sources for PPy, were coated on SWCNT, along with methyl orange (MO) as a surfactant and ferric chloride as an initiator. The optimum value of Py for maximum TE performance was determined. The results showed that the SWCNT acted as a core template to direct the self-assembly of PPy and also to further enhance TE performance. The TE power factor, PF, and figure of merit, zT, values of the pure PPy were initially recorded as ~1 µW/mK2 and 0.0011, respectively. These values were greatly increased to 360 µW/mK2 and 0.09 for the optimized core shell nanocomposite sample. The TE power generation characteristics of the fabricated single-leg module of the optimized sample were also investigated and confirmed these findings. This enhancement was attributed to the uniform coating and good interaction between PPy polymer chains and walls of the SWCNT through π-π stacking. The significant enhancement in the TE performance of SWCNT/PPy nanocomposite is found to be superior compared to those reported in similar composites, which indicates that this nanocomposite is a suitable and scalable TE material for TE power generation.

Thermal Analysis of a Metal-Organic Framework ZnxCo1-X-ZIF-8 for Recent Applications.

Zeolitic imidazolate frameworks (ZIFs) are interesting materials for use in several aspects: energy storage material, gas sensing, and photocatalysis. The thermal stability and pyrolysis process are crucial in determining the active phase of the material. A deep understanding of the pyrolysis mechanism is in demand. Therefore, the thermodynamics and combustion process with different heating rates was examined, and the kinetic parameters were computed employing thermogravimetric tests. Based on the TG analysis of combustion, pyrolysis moves to the high-temperature region with an increase in heating rate. The decomposition process can be separated into the dehydration (300-503 K) and the pyrolysis reaction (703-1100 K). Three points of the decomposition process are performed by dynamical analysis owing to shifts of slopes, but the combustion process has only one stage. The Zeolitic imidazolate framework's structure properties were examined using TDDFT-DFT/DMOl3 simulation techniques. Dynamical parameters, for instance, the possible mechanism, the pre-exponential factor, and the apparent activation energy are obtained through comparison using the Kissinger formula. The thermodynamics analysis of the Zn1-xCox-ZIF-8 materials is an effective way to explore the temperature influence on the process of pyrolysis, which can benefit several environment purifications, photocatalyst, and recent applications.

Graphene and Carbon Nanotubes Fibrous Composite Decorated with PdMg Alloy Nanoparticles with Enhanced Absorption-Desorption Kinetics for Hydrogen Storage Application.

We describe a graphene and fibrous multiwall carbon nanotubes (f-MWCNT) composite film prepared by plasma-enhanced chemical vapor deposition for use as a suitable and possible candidate of hydrogen storage materials. A high storage capacity of 5.53 wt% has been obtained with improved kinetics. The addition of binary PdMg alloy nanoparticles to the surface of graphene-fibrous nanotubes composite films raised the storage capacity by 53% compared to the film without PdMg decorated nanoparticles. Additionally, the graphene/f-MWCNT composite film decorated with PdMg nanoparticles exhibited an enhanced hydrogen absorption-desorption kinetics. The fibrous structure of the MWCNTs, alongside graphene sheets within the film, creates an enormous active region site for hydrogen reaction. The addition of PdMg nanoparticles enhanced the reaction kinetics due to the catalytic nature of Pd, and increased the hydrogen content due to the high absorption capacity of Mg nanoparticles. The combination of Pd and Mg in a binary alloy nanoparticle enhanced the hydrogen capacity and absorption-desorption kinetics.

In situ printing of scaffolds for reconstruction of bone defects.

Bone defects are commonly caused by traumatic injuries and tumor removal and critically sized defects overwhelm the regenerative capacity of the native tissue. Reparative strategies such as auto, xeno, and allografts have proven to be insufficient to reconstruct and regenerate these defects. For the first time, we introduce the use of handheld melt spun three dimensional printers that can deposit materials directly within the defect site to properly fill the cavity and form free-standing scaffolds. Engineered composite filaments were generated from poly(caprolactone) (PCL) doped with zinc oxide nanoparticles and hydroxyapatite microparticles. The use of PCL-based materials allowed low-temperature printing to avoid overheating of the surrounding tissues. The in situ printed scaffolds showed moderate adhesion to wet bone tissue, which can prevent scaffold dislocation. The printed scaffolds showed to be osteoconductive and supported the osteodifferentiation of mesenchymal stem cells. Biocompatibility of the scaffolds upon in vivo printing subcutaneously in mice showed promising results. STATEMENT OF SIGNIFICANCE.

Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds.

Non-healing wounds have placed an enormous stress on both patients and healthcare systems worldwide. Severe complications induced by these wounds can lead to limb amputation or even death and urgently require more effective treatments. Electrospun scaffolds have great potential for improving wound healing treatments by providing controlled drug delivery. Previously, we developed fibrous scaffolds from complex carbohydrate polymers [i.e. chitin-lignin (CL) gels]. However, their application was limited by solubility and undesirable burst drug release. Here, a coaxial electrospinning is applied to encapsulate the CL gels with polycaprolactone (PCL). Presence of a PCL shell layer thus provides longer shelf-life for the CL gels in a wet environment and sustainable drug release. Antibiotics loaded into core-shell fibrous platform effectively inhibit both gram-positive and -negative bacteria without inducting observable cytotoxicity. Therefore, PCL coated CL fibrous gel platforms appear to be good candidates for controlled drug release based wound dressing applications.