Narrow Diameter Distribution Research Articles

Remote-Contact Catalysis for Target-Diameter Semiconducting Carbon Nanotube Arrays.

Electrostatic catalysis uses an external electric field (EEF) to rearrange the charge distribution to boost reaction rates and selectively produce certain reaction products in small-molecule reactions (e.g., Diels-Alder addition), requiring a 10 MV/cm field aligned with the reaction axis. Such a large and oriented EEF is challenging for large-scale implementation or material growth with multiple reaction axes or steps. Here, we demonstrate that the energy band at the tip of an individual single-walled carbon nanotube (SWCNT) can be spontaneously shifted in a high-permittivity growth environment, with its other end in contact with a low-work-function electrode (e.g., hafnium carbide). By adjusting the Fermi level at a point where there is a substantial disparity in the density of states (DOS) between semiconducting (s-) and metallic (m-) SWCNTs, we achieve effective electrostatic catalysis for 99.92% purity s-SWCNT growth with a narrow diameter distribution (0.95 ± 0.04 nm), targeting the requirement of advanced SWCNT-based electronics for future computing.

Selenium Dioxide Catalyzed Polymerization of N‐doped Poly(benzodifurandione) (n‐PBDF) and Its Derivatives

AbstractThe recent discovery of highly conductive, solution‐processable, n‐doped poly(benzodifurandione) (n‐PBDF) marks a milestone in the development of conducting polymers. Currently, n‐PBDF is prepared by either duroquinone‐mediated or copper‐catalyzed polymerizations, where scalability and cost‐effectiveness may present challenges. Here, we report a general, scalable, and cost‐effective method for n‐PBDF and its derivatives, namely selenium dioxide (SeO2) catalyzed polymerization. We discovered that a catalytic amount of selenium dioxide leads to high monomer conversions (>99 % by NMR). The obtained n‐PBDF exhibits a consistently narrow hydrodynamic diameter distribution and its thin films show high conductivities. Furthermore, we revealed that this polymerization involves a mechanism distinct from the previously reported radical pathway. It involves successive Riley oxidation and aldol polycondensation processes. It was also found that the reduced selenium precipitates from dimethyl sulfoxide (DMSO) when the catalytic cycle is terminated, allowing for a straightforward purification process through centrifugation and filtration. This method thus eliminates the need for the costly and slow dialysis process. Finally, we demonstrated that SeO2 catalyzed polymerization is applicable to n‐PBDF derivatives, proving the generality of this method.

Selenium Dioxide Catalyzed Polymerization of N-doped Poly(benzodifurandione) (n-PBDF) and Its Derivatives.

The recent discovery of highly conductive, solution-processable, n-doped poly(benzodifurandione) (n-PBDF) marks a milestone in the development of conducting polymers. Currently, n-PBDF is prepared by either duroquinone-mediated or copper-catalyzed polymerizations, where scalability and cost-effectiveness may present challenges. Here, we report a general, scalable, and cost-effective method for n-PBDF and its derivatives, namely selenium dioxide (SeO2) catalyzed polymerization. We discovered that a catalytic amount of selenium dioxide leads to high monomer conversions (>99 % by NMR). The obtained n-PBDF exhibits a consistently narrow hydrodynamic diameter distribution and its thin films show high conductivities. Furthermore, we revealed that this polymerization involves a mechanism distinct from the previously reported radical pathway. It involves successive Riley oxidation and aldol polycondensation processes. It was also found that the reduced selenium precipitates from dimethyl sulfoxide (DMSO) when the catalytic cycle is terminated, allowing for a straightforward purification process through centrifugation and filtration. This method thus eliminates the need for the costly and slow dialysis process. Finally, we demonstrated that SeO2 catalyzed polymerization is applicable to n-PBDF derivatives, proving the generality of this method.

Diameter-Controlled Synthesis of Carbon Nanotubes Using [2n]Collarenes as Rigid Organic Templates.

An effective route to diameter-controlled single-walled carbon nanotubes (SWCNTs) remains elusive. The use of organic templates to precisely control the diameter of the resulting nanotubes holds great promise in this regard but has hitherto had very limited practical success. A main obstacle is the limited availability of suitable organic templates. Here, we report the diameter-controlled bottom-up synthesis of SWCNTs with elaborately designed [2n]collarenes, hydrocarbon belts consisting of alternating phenylene and 1,4-cyclohexadiene rings, as rigid organic templates. A new approach has been developed to construct these collarenes, which are then used as templates in the bottom-up growth of SWCNTs. The resulting SWCNTs exhibit narrow diameter distributions, matching the diameters of the employed collarene templates. This work greatly propels the synthesis of diameter-controlled SWCNTs.

Impact of deep eutectic solvent pre-treatment on the extraction of cellulose nanofibers

Deep Eutectic Solvents (DESs) have emerged as promising eco-friendly pre-treatment agents for lignocellulosic biomass, offering considerable advantages for the nanofibrillation process. This study investigates the impact of DESs on cellulose fibers morphology, focusing on solubilization phenomena in the amorphous regions that may facilitate cellulose nanofiber production. The pre-treatment process combining a DES (triethylmethylammonium chloride and imidazole, TEMA:IMD) with microwave (MW) energy was optimized to enhance the solubility of cellulosic fibers. A response surface methodology (RSM) was employed to optimize the DES-MW-assisted pre-treatment. Results show that the reaction time and the temperature significantly influence the solubility of cellulosic fibers. The optimized conditions resulted in cellulose fibers with low content of hemicellulose and lignin, high crystallinity index, and improved thermal stability. The effectiveness of DES-MW pre-treatment in producing cellulose nanofibers (CNFs) from native and pre-treated fibers was investigated. Cellulose fibers pre-treated with a DES yielded CNFs with a narrower diameter distribution. Overall, optimized DES-MW pre-treatment offers a promising strategy for the efficient and sustainable extraction of CNFs.

Controlled growth of single-walled carbon nanotubes with narrow diameter distribution and high areal density on Mn-doped ZrO2-supported Fe catalyst

Single-walled carbon nanotubes (SWCNTs) with a narrow diameter distribution and high areal density hold great promise for a variety of applications, particularly in advanced electronics and biomedical devices. This study utilizes Mn ion doping as a strategic approach both to stabilize the ZrO2-supported Fe catalyst and regulate lattice oxygen release, thereby facilitating the growth of SWCNTs with high areal density and a narrow diameter distribution. The ZrO2-supported Fe catalyst was meticulously dispersed on Si/SiO2 (300 nm) substrates through the optimization of spin-coating speed and solvent viscosity, aiming to enhance the dispersion and uniformity. Investigation into the precise control over the Mn ion content was conducted to regulate the structure and stability of the Mn-doped ZrO2-supported Fe catalyst. Mn ions perform a dual role: they maintain a higher proportion of ZrO2 in the monoclinic phase, which in turn alleviates the monoclinic-tetragonal phase transition during chemical vapor deposition (CVD) growth. Concurrently, the conversion of Mn3+ to Mn4+ ions captures the lattice oxygen released during the formation of zirconium transition oxides. Additionally, first-principles simulations have confirmed the stabilizing impact of Mn ions on the catalyst, which reduces aggregation and maturation, ultimately resulting in a more concentrated diameter distribution of as-grown SWCNTs. This approach has successfully achieved the controlled growth of high areal density SWCNTs with a diameter distribution of 1.73 ± 0.08 nm.

Fuel reactor simulation for coal chemical looping process: Effects of ash on flow behavior

Chemical looping gasification (CLG) is an environmentally friendly strategy for using coal that has significant promise for application in reality. Nevertheless, the process of generating and accumulating ash from coal presents obstacles to the advancement of this technology. To fully comprehend the effects of ash from coal on the internal flow properties of a fuel reactor (FR). The Computational Particle Fluid Dynamics (CPFD) approach was applied to predict the CLG with coal at the FR, uncovering distinctive flow properties of gas-solid reactions. This study investigated the effects of ash particles content, polydispersity and sphericity on the flow behavior within the bed. The simulation accurately predicted the motion of the bubbles within the FR, and the gas phase composition distribution at the outlet is closer to the experimental data. Introducing coal ash creates a reduction in the concentration of ilmenite, resulting in a drop in the rates of the related reactions. The narrow particles diameter distribution among coal ash facilitates the particles arrangement in the bed and improves the overall reaction. The addition of moderately irregular-shaped coal ash particles has a certain positive effect on improving the gas-solid contact.

Eco-Friendly Superhydrophobic Modification of Low-Cost Multi-Layer Composite Mullite Base Tubular Ceramic Membrane for Water Desalination

This study aimed to investigate and develop a cost-effective and superhydrophobic ceramic membrane for direct contact membrane distillation (DCMD) applications. Two types of mullite-based composite membranes were prepared via extrusion and sintering techniques. To create a small and narrow pore diameter distribution on the membrane surface, the dip-coating technique with 1 µm alumina was employed. The hexadecyltrimethoxysilane eco-friendly grafting agent was adopted to modify low-cost multilayer mullite-based composite membranes, transforming them from hydrophilic to superhydrophobic. The prepared membranes were characterized via field emission scanning electron microscopy (FESEM), energy-dispersive spectrometry (EDS), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray diffraction (XRD), liquid entire pressure (LEP), contact angle, atomic force microscopy (AFM), porosity, and membrane permeability. The results of the prepared membranes validate the appropriateness of the material for membrane distillation applications. The optimized membrane, with a contact angle of 160° and LEP = 1.5 bar, was tested under DCMD using a 3.5 wt.% sodium chloride (NaCl) synthetic solution and Persian Gulf seawater as a feed. Based on the acquired results, an average permeate flux of 3.15 kg/(m2·h) and salt rejection (R%) of 99.62% were found for the 3.5 wt.% NaCl solution. Moreover, seawater desalination showed an average permeate flux of 2.37 kg/(m2·h) and salt rejection of 99.81% for a 20-h test without any pore wetting. Membrane distillation with a hydrophobic membrane decreased the turbidity of seawater by 93.13%.

Central Composite Design and Response Surface Methodology for Optimizing the Diameter of Electrospun Polyamide-6,6 Nanofiber Mat

Electrospinning is a well-established technique for creating submicron polymer fibers to create distinctive functional nanostructures. Electrospinning parameters including solution concentration, tip-to-collector distance and applied voltage are adjusted to produce nonwovens with variable fiber diameter distributions. This research on the response surface methodology (RSM) is being used to model the diameter of a polyamide-6,6 (PA-6,6) nanofiber mat. The experiments were designed using central composite design (CCD) and RSM, which evaluated the interactions between the operating variables (polymer concentration, applied positive voltage, needle tip to collector distance and spinning angle) on the diameter of the PA-6,6 nanofiber. The average nanofiber diameter increased as the concentration of the PA-6,6 polymer solution increased. The model’s strong regression coefficient ([Formula: see text]) reveals that it did a desirable of predicting the diameter of PA-6,6 fibers. The experimental findings and predicted fiber diameters were in good agreement. The results demonstrate that the optimization of electrospinning process to produce the smallest nanofibers and narrowest diameter distribution ([Formula: see text]) combined effects of 10% polymer concentration, 21[Formula: see text]kV applied positive voltage, 18[Formula: see text]cm needle tip to collector distance and 60[Formula: see text] spinning angle are substantial interacting effects that have an impact on the surface response nanofibers. The results of the research and several mathematical models will offer useful guidelines for choosing parameter settings for electrospinning PA-6,6 to achieve the required fiber diameter. By saving time, effort and money more effectively, this research will expand the field of investigation for the quality of electrospun nanofibers.

Gas CO2 foaming and intermixing in portland cement paste to sequester CO2

In this study, concentrated CO2 gas was used to create foamed cement paste, and concentrated CO2 gas was intermixed in fresh cement paste to produce regular cement paste materials that were not foamed. The potential of both methods to form CaCO3 from calcium ions that would form Ca(OH)2 was investigated. After curing the materials for different ages, the Ca(OH)2 and CaCO3 contents were measured using thermogravimetric analysis; the large void size distributions, dynamic modulus, and compressive strength were tested and compared against Control (no gas added), and N2 foamed and N2 intermixed specimens. A 10% increase in dynamic modulus and compressive strength was measured in CO2 foamed specimens compared to N2 foamed specimens. The increase in mechanical properties was the result of both a narrow void diameter distribution and CaCO3 formation in place of Ca(OH)2. The CO2 foamed cement generation method shows the potential to sequester 0.06 ton of CO2 for every ton of cement which is a CO2 emission reduction of 7.0% of the CO2 production associated with cement production. For the CO2 intermixing method, the void content, compressive strength, and dynamic modulus results were consistent between the Control and CO2 intermixed specimens while the N2 intermixed specimens showed a decrease in compressive strength and dynamic modulus. The CO2 intermixing method showed potential to sequester 0.04 ton of CO2 for every ton of cement or a 4.7% CO2 emission reduction of the total CO2 production associated with cement manufacturing. The reported CO2 emissions are not based on life cycle assessment and do not account for emissions associated with CO2 collection, transportation, and intermixing. The present paper does not investigate the mechanisms of hydration under CO2 intermixing.

Hybrid processing of melt electrospinning/blowing for polypropylene/polyethylene glycol fiber fabrication with various diameter distribution

Many studies have been conducted to develop and optimize the manufacturing process of polymer fibers in various forms. In particular, many melt-spinning processes have been developed for the manufacture of nanofibers of polymer materials with excellent chemical resistance. In this study, we investigated the effects of various spinning conditions and their spinning behavior on the fiber manufacturing process and properties using a melt electrospinning/blowing process that combines conventional melt blowing and electrospinning. We also report a discontinuous spinning process that produces a web with a very wide diameter distribution from the nanoscale to the microscale with gradient fibers. They are generally compared with webs, which have a narrow diameter distribution. We believe that by using this process, it is possible to produce diameters of various distributions in one step. These results show remarkable potential for many applications in which gradient fibers are required.

Monodispersed, Micron-Sized Supermicroporous Silica Particles by Cetyltrimethylammonium Bromide-Mediated Preparation.

In this study, we present a novel modified Stöber method utilizing cetyltrimethylammonium bromide (CTAB) as a mediator for the preparation of monodispersed, micron-sized supermicroporous silica particles. Observed results show prepared silica particles ranging in size from 0.64 to 1.36 μm with an increase in CTAB concentration from 1.0 to 5.0 mM. The particles exhibited low polydispersity (<5%), a high Brunauer-Emmett-Teller surface area (570 to 1064 m2/g), and pore volumes ranging from 0.22 to 0.39 cm3/g. The pore size, determined using the Barrett-Joyner-Halenda method from the adsorption branches of the isotherms, was approximately 1.9 nm, specifically 1.83, 1.85, and 1.90 nm, as the CTAB concentration increased from 1.0 to 2.5 and 5.0 mM, respectively. The resulting particles displayed a narrow distribution of pore diameters. In addition, to obtain an in-depth understanding of the role of CTAB on the preparation of silica particles, a possible mechanism is also investigated using conductivity, dynamic light scattering (DLS), zeta potential, FT-IR spectra, and transmission electron microscopy. Our findings demonstrate that CTAB plays multiple roles in the hydrolysis/condensation of TEOS (tetraethyl orthosilicate) and subsequent nucleation and growth of silica particles. CTAB acts as a template for superporosity, a stabilizer for colloids, and an accelerator for nucleation and growth, leading to formation of monodispersed micrometer silica particles. Further characterization through FT-IR and 29Si solid NMR spectra revealed that the micron silica particles were obtained with inhomogeneity in the condensation degree, allowing for selective etching through hot incubation to form micron-sized hollow silica spheres.

Iterative Strategy for Sorting Single-Chirality Single-Walled Carbon Nanotubes from Aqueous to Organic Systems.

Significant advancements in electronic devices and integrated circuits have been facilitated by semiconducting single-walled carbon nanotubes (SWCNTs) sorted by conjugated polymers (CPs). However, the variety of CPs with single-chirality selectivity is limited, and the sorting results are strongly dependent on the chiral distribution of the starting materials. To address this, we develop an iterative strategy to achieve single-chirality SWCNT separation from aqueous to organic systems, based on a multistep tandem extraction technique that allows a gentle and nondestructive separation of surfactants from SWCNTs, ensuring an efficient system transfer. In parallel, we refined the iterative sorting process between CPs. Employing two starting materials with narrow diameter distributions, using three CPs, we successfully sorted out five single-chirality SWCNTs of the (9,5), (8,6), (10,5), (8,7), and (11,3) species in organic systems. This strategy bridges the gap between aqueous and organic separation systems, achieving efficient complementarity between them.

Synthesis and characterization of new electrospun medical scaffold-based modified cellulose nanofiber and bioactive natural propolis for potential wound dressing applications.

Recently, the design of polymer nanofibers using the electrospinning process has attracted much interest. Particularly the use of natural polymers has promoted many advantages in their biomedical applications. However, the combination of multiple natural polymers remains a great challenge in terms of electrospun production and applied performance. From this perspective, the current investigation highlights the study of the preparation of electrospun nanomaterial scaffolds based on combined natural polymers for improved wound healing performance. First, we have synthesized a crosslinked polymer by reacting microcrystalline cellulose (MC) and chitosan (CS) biopolymer via the intermediate of citric acid as a crosslinking agent. Then a natural propolis biomolecule was incorporated into the polymer network. Different MC/CS blend ratios of 90/10 and 70/30 were then used and various machine parameters were optimized to obtain nanofiber scaffolds with excellent strength and structures. SEM, IR, physicochemical, mechanical, and morpho-logical characterization were then performed. SEM evaluation revealed homogeneous and bead-free nanofibrous structures, with well-defined morphology and a random deposition that could accurately mimic the extracellular matrix of native skin. The calculated average nanofiber diameters for the MC/CS blend ratios at 90/10 and 70/30 were 431.4 and 441.2 nm, respectively. The results showed that when the chitosan amount increased, larger nanofibers with narrow diameter distribution appeared. The prepared nanomaterials had a significant and close water vapor permeability of about 1735.12 and 1698.52 g per m per day for the two blend ratios of 90/10 and 70/30, respectively. The examination of swelling behavior revealed a noteworthy enhancement in hydrophilicity, a necessary attribute for improved healing efficacy. FT-IR analysis confirmed the success and the stability of the chemical crosslinking reaction between the two biopolymers before nanofiber conception. Excellent mechanical properties were acquired, based on the chitosan content. Both developed nanofiber scaffolds exhibited high tensile strength and Young's modulus values. The incorporation of 30% chitosan versus 10% results in an increase in tensile strength of 11% and 14% in Young's modulus. Therefore, we could adjust the different mechanical properties simply by varying the mixing rate of the electrospun polymers. Using epithelial HepG2 cells, viability and kinetic cell adhesion assays were assessed to obtain biological evaluation. No cytotoxicity was observed and good cytocompatibility was confirmed. Functionalized nanofiber biomaterials with different MC/CS ratios substantiated significant bactericidal effectiveness against Gram-positive and Gram-negative bacterial culture strains. The novel functional electrospun wound dressing scaffold demonstrated effective and promising biomedical performance, healing both acute and chronic wounds.

MgH2 nanoparticles confined in reduced graphene oxide pillared with organosilica: a novel type of hydrogen storage material.

Hydrogen is a promising alternative fuel that can push forward the energy transition because of its high energy density (142 MJ kg-1), variety of potential sources, low weight and low environmental impact, but its storage for automotive applications remains a formidable challenge. MgH2, with its high gravimetric and volumetric density, presents a compelling platform for hydrogen storage; however, its utilization is hindered by the sluggish kinetics of hydrogen uptake/release and high temperature operation. Herein we show that a novel layered heterostructure of reduced graphene oxide and organosilica with high specific surface area and narrow pore size distribution can serve as a scaffold to host MgH2 nanoparticles with a narrow diameter distribution around ∼2.5 nm and superior hydrogen storage properties to bulk MgH2. Desorption studies showed that hydrogen release starts at relatively low temperature, with a maximum at 348 °C and kinetics dependent on particle size. Reversibility tests demonstrated that the dehydrogenation kinetics and re-hydrogenation capacity of the system remains stable at 1.62 wt% over four cycles at 200 °C. Our results prove that MgH2 confinement in a nanoporous scaffold is an efficient way to constrain the size of the hydride particles, avoid aggregation and improve kinetics for hydrogen release and recharging.

Synthesis of Cadmium Oxyorthosilicate by a Sol-Gel Method

Cadmium silicates are materials of interest due to their stability and possible application as phosphors. There are three stable forms: cadmium metasilicate, CdSiO3, cadmium orthosilicate, Cd2SiO4 and cadmium oxyorthosilicate, Cd3SiO5. Of these, oxyorthosilicate is particularly challenging to obtain, leading to fewer studies. We have successfully prepared Cd3SiO5 using a sol-gel approach, employing cadmium acetate and tetraethylorthosilicate as precursors in a stoichiometric proportion of 2:1. Additionally, cetyltrimethylammonium bromide served as a template for creating a mesoporous structure. Adjusting the pH to 3 and subjecting the material to calcination at 800 °C for 6 h, we achieved the formation of cadmium oxyorthosilicate compound, identified by X-ray diffraction. Electron diffractometry and energy dispersive X-ray spectrometry confirm the phase purity. Characterization via nitrogen adsorption analysis and transmission microscopy shows aggregates of nanoparticles with a surface area of 6 m2 g-1 and a narrow pore diameter distribution centered at 5 nm.

Numerical simulation for electric field intensity and jet space of the quadratic spiral spinneret with auxiliary electrode

To produce a high quality electrostatic spinneret with low voltage requirements, low energy consumption, and narrow fiber diameter distribution, the mechanical model of the spinning unit of the fractal spiral spinneret was established by using the quadratic fractal spiral parametric equation. The established fractal spiral electrostatic spinning model was imported into COMSOL Multiphysics finite element analysis software, mesh division was performed on the model, multiple spinning units were combined to form the array spinneret, and the optimal parameters of the fractal structure were optimized. However, there are still two sides of the field intensity other than the middle field intensity of the high situation. In order to equalize the field intensity, we used the spinneret properties of the same disc auxiliary electrode and quadratic fractal spiral spinneret in a linear arrangement, and the auxiliary electrode and spinneret distance and spinneret radius of the two important parameters to optimize the simulation, resulting in obtaining a more uniform field intensity distribution of the quadratic fractal spiral spinneret electrospinning equipment. Based on the calculation of the fractional dimension of the Von Koch curve, the fractional dimension of the quadratic fractal spinneret was 1.77. The critical field intensity of the system was calculated to be 2.13 × 106 V/m, and the jet space was 1.22–3.13 mm. The optimized quadratic fractal spinneret model with auxiliary electrode faced the receiving plate in the range of 60° from the left to the right of the spinning sites, –5 to 5 sites, which may emit the spinning jet.

Controlled spherical deuterium droplets as Lagrangian tracers for cryogenic turbulence experiments.

The study of the smallest scales of turbulence by (Lagrangian) particle tracking faces two major challenges: the requirement of a 2D or 3D optical imaging system with sufficiently high spatial and temporal resolution and the need for particles that behave as passive tracers when seeded into the flow. While recent advances in the past decade have led to the development of fast cameras, there is still a lack of suitable methods to seed cryogenic liquid helium flows with mono-disperse particles of sufficiently small size, of the order of a few micrometers, and a density close enough to that of helium. Taking advantage of the surface tension, we propose two different techniques to generate controlled liquid spherical droplets of deuterium over a liquid helium bath. The first technique operates in a continuous mode by fragmenting a liquid jet, thanks to the Rayleigh-Taylor instability. This results in the formation of droplets with a diameter distribution of 2 ± 0.25DN, where DN is the diameter of the jet nozzle (DN = 20μm in the present experiment). This method offers a high production rate, greater than 30kHz. The second technique operates in a drop-on-demand mode by detaching droplets from the nozzle using pressure pulses generated using a piezoelectric transducer. This approach yields a much narrower diameter distribution of 2.1 ± 0.05DN but at a smaller production rate, in the range 500 Hz-2kHz. The initial trajectories and shapes of the droplets, from the moment they are released from the nozzle until they fall 3mm below, are investigated and discussed based on back-light illumination images.

Facile characterization of metallic impurities in detonation nanodiamonds through selective combustion using standard techniques

Detonation nanodiamonds are sp3 carbon nanomaterials with narrow diameter distribution. They have high potential of application in various fields like nanomedecine, advanced composites and lubricants, photocatalysis. Detonation nanodiamonds unfortunately contain metallic and inorganic impurities of diverse nature which can act as “Trojan horses” and even at weak content, they can significantly impact the nanodiamonds efficiency and the searched performances. Detection and quantification as well as subsequent removal of these impurities is highly difficult due to the lack of tools available by scholars. In this work, we propose a useful approach to detect and identify the inorganic impurities in detonation nanodiamonds. Our method which consists in a selective combustion of the nanodiamonds results in concentrating these impurities is a one-step and simple method. This approach, transferable to other kinds of carbon nanomaterials, is proved to be a valuable way allowing analysis of detonation nanodiamonds by standard characterization techniques such as X-ray Photoelectron Spectroscopy, Fourier Transform Infra-Red and Raman spectroscopies or Powder X-Ray Diffraction, available in any material science laboratory.

Centrifugal Microfluidic Synthesis of Nickel Sesquioxide Nanoparticles.

Nickel sesquioxide (Ni2O3) nanoparticles were synthesized using centrifugal microfluidics in the present study. The obtained nanoparticles were characterized using SEM to investigate their morphology and microstructure, and XRD was employed to analyze their purity. The nanoparticle size data were measured and analyzed using ImageJ (v1.8.0) software. The flow process and mixing procedure were monitored through computational fluid dynamics simulation. Among the synthesized Ni2O3 nanoparticles, those obtained at the rotation speed of 1000 rpm for 10 min with angular acceleration of 4.2 rad/s2 showed the best performance in terms of high purity, complete shape and microstructure, small diameter, and narrow diameter distribution. The experimental results demonstrate that the rotation speed of the microfluidic chip and reaction time contribute to a decrease in particle diameter and a narrower diameter distribution range. In contrast, an increase in acceleration of the rotation speed leads to an expanded nanoparticle size range and, thus, a wider distribution. These findings contribute to a comprehensive understanding of the effects exerted by various factors in centrifugal microfluidics and will provide new insights into nanoparticle synthesis using centrifugal microfluidic technology.