Particle Morphology Research Articles

Enhanced electrochemical performance of the LiMn0.6Fe0.4PO4/C modified by secondary particle morphology control combined with primary particle size control

Enhanced electrochemical performance of the LiMn0.6Fe0.4PO4/C modified by secondary particle morphology control combined with primary particle size control

Development of dexibuprofen loaded nano transfersomal gel with enhanced biopharmaceutical performance in complete Freund's adjuvant induced arthritis model

The purpose of this study was to enhance the biopharmaceutical performance of Dexibuprofen (DXI) using transfersomal gel (DXI-TG) as drug delivery system. DXI loaded transfersomes (DXI-T) were prepared via thin film technique, characterized for particle size, polydispersity index, zeta potential, particle morphology and entrapment efficiency. The DXI-T was further incorporated into 2 % (w/v) chitosan gel to get the final dosage form DXI-TG, which was characterized for homogeneity, pH, spread-ability and rheological properties. In vitro release, ex vivo permeation and in vivo studies were also conducted along with stability study of the optimized formulation. DXI-T showed excellent vesicle properties including, size distribution (235.1 ± 4.66 nm), poly dispersity index (0.184 ± 0.001), zeta potential (−10.5 ± 0.23 mV) and entrapment efficiency (82.9 ± 1.07 %). TEM analysis exhibited spherical morphology and uniformly distributed nanoparticles, whereas FTIR showed no bond anomalies. DXI-TG showed suitable gel properties with a viscosity of 11310 ± 20 cP, pH 5.2 ± 0.3, good homogeneity, non-Newtonian flow behavior, good spread-ability (298 ± 7.63 %) and high drug content (97.01 ± 3.1 %). in vitro release studies demonstrated that DXI-TG has significantly controlled the release of DXI when compared with DXI-T, DXI-G and DXI-Suspension at pH 5.5 and 7.4. Similarly, ex vivo permeation analysis showed meaningfully increased permeation of DXI-T followed by DXI-TG when compared with test formulations. Like normal control group, skin irritation studies showed no erythema and edema in DXI-TG treated group. Additionally, DXI-TG demonstrated a significantly enhanced bioavailability (5-fold) when compared with DXI-Suspension and DXI-G. Furthermore, DXI-TG showed significantly enhanced therapeutic effect against acute arthritis model when compared with DXI-Suspension and DXI-G. Besides, no signs of evident toxicity on major body organs was observed in DXI-TG treated animal group. Also, the DXI-TG was found stable for a period of 6 months. It can be concluded that transfersomal gel may be a suitable carrier for DXI with enhanced bioavailability, improved therapeutic efficacy and no evident toxicity as exhibited in this study.

Green low-cost synthesis of zero-valent iron nanoparticles from Palm Petiole Extract for Cr(VI) removal from water.

One of the hottest research topics over the last decades was the valorization or/and recycling of agro-industrial wastes into different valuable liquid or solid products, which is considered a sustainable and low-cost approach. In this study, we developed zero-valent iron nanoparticles from Palm Petiole Extract (P-NZVI) using a green and straightforward approach. The as-synthesized P-NZVI was used to adsorb Cr(VI) in water. The physico-chemical characterizations of P-NZVI, including the particle size, crystalline structure, surface area, morphology, and functional groups, were investigated via several techniques such as UV-vis spectroscopy, SEM, TEM, XRD, FTIR, AFM, DLS, pHZPC measurement, and BET analysis. The adsorption performance of P-NZVI was studied under different operational parameters, including pollutant concentration, pH, temperature, and adsorbent mass. The adsorption rate was found to be 89.3% within 40 min, corresponding to the adsorption capacity of 44.47 mg/g under the following conditions: initial Cr(VI) concentration of 40 mg/L, pH 5, and a P-NZVI dosage of 1 g/L. It was found that the adsorption pattern follows the Langmuir and the pseudo-second-order kinetic models, indicating a combination of monolayer adsorption and chemisorption mechanisms. The thermodynamic study shows that the adsorption process is endothermic and spontaneous. The reusability of P-NZVI was carried out four times, showing a slight decrease from 89.3 to 87%. These findings highlight that P-NZVI's could be an effective green adsorbent for removing Cr(VI) or other types of toxic pollutants from water.

Multi-scale characterization of lead-rich deposited particles originating from the fire of Notre-Dame de Paris

Fire is a major hazard for built heritage. The fire at Notre-Dame on April 15, 2019 completely destroyed the woodframe and the lead roof (about 285 tons) almost entirely melted due to high temperatures. A part of the molten lead escaped into the atmosphere in the form of aerosols while the majority remains within cathedral enclosure in the form of deposits, metallic remains, spatters etc. In particular unusual yellowish deposits of lead-rich particles were observed and collected inside the monument (in the nave, near the organ and in St-Eloi Chapel). These were then thoroughly characterized to identify the neoformed lead compounds. Both bulk and local analyses were carried out to obtain particle morphology and size distribution, chemistry and mineralogy of the deposits, from macro to nanoscale. We found that the fire-related deposits all contain high amount of lead (10 to 44 %) mainly in the form of monoxides (litharge and massicot) with other lead-bearing phases (Ca-plumbate, metallic lead, lead sulfates and carbonates, plattnerite) in smaller amount. These lead phases are concentrated in heterogeneous microspheres, at the periphery of terrigenous minerals (calcite, quartz, feldspars) or mixed with anhydrite minerals. The size distribution shows that the fire produced giant particles (> 100 μm in diameter) similar to those found near the fallout from industrial emissions. This study provides a better understanding of the lead contamination pathways following the Notre-Dame cathedral fire and new insights into the reactivity of lead during a fire.

Ceramic fused filament fabrication (CF3) of alumina: Influence of powder particle morphology on processing and microstructure

This study investigates ceramic fused filament fabrication (CF3) 3D printing of alumina with an emphasis on the impact of particle morphology on feedstock preparation and printability. Spherical powder displayed superior flow with higher apparent density, tap density, and powder packing fraction compared to irregular powder. A 55 vol % powder loading was chosen to ensure good flowability during printing. Irregular powder-based feedstocks had 40X higher viscosity than spherical powder feedstocks at 400 s−1 shear rate, posing potential printing challenges. Slow printing speed maintained low feed-rates for consistent material flow. The debinding and sintering process produced macroscopically defect-free alumina components with relative densities above 89 % for both powder morphologies. The focus of the work is on comparing two different powder particle morphologies influencing feedstock behavior, printing fidelity, and sintered part properties.

Study on the effect of sodium removal from citric acid pretreated red mud on the physical properties of red mud.

Red mud is a highly alkaline solid waste discharged from the alumina industry, and its high sodium content is the key factor limiting its wide utilization. Therefore, effective control of the "frosting" phenomenon during the application of red mud has received significant attention. In this study, the changes of particle size, phase, morphology, and pore size of red mud after sodium removal with different amounts of citric acid pretreatment were investigated. The single-factor experiment shows that the Na+ leaching rate is 86.33% under a citric acid dosage of 15%, liquid-to-solid ratio of 7mL/g, leaching temperature of 80°C, stirring speed of 300rpm, and leaching time of 10min. The leachate is characterized through X-ray diffraction (XRD), scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) surface area analysis. The results reveal that Na+ mainly exists in a combined state in the form of cancrinite. With the increase of citric acid dosage, red mud agglomerates, calcite, and cancrinite are dissolved, and new phases such as calcium oxalate and magnesium aluminum hydroxide are formed. The specific surface area, pore volume, and pore diameter show irregular changes with the increase in the citric acid dosage. Citric acid pretreatment can effectively reduce the sodium content in red mud, the treatment cost of leaching solution is low, and the leaching residue is neutral, which is helpful to promote the practical application of red mud.

Particle morphology of alkali metal chloride salts in induction heating based pulsed spray drier: Experimental analysis and ANN prediction

Hygroscopic nature of alkali metal chloride salts makes attaining mono-sized dried particles from their aqueous precursor solution an engineering challenge for conventional co-current or counter-current spray driers. Conventional spray driers offer better thermal utilization in either the spray zone or dried particle zone depending on their configuration viz. co-current or counter-current, respectively. In this work, an alternative prototype named induction heating based pulsed spray drier (IH-PSD) is proposed to obtain dry alkali metal chloride salt powders with narrow particle size distribution. Laser diffraction analysis is carried out for initial droplet size distribution whereas scanning electron microscopy and sieve shaker analysis is carried out for studying the particle morphology and particle size distribution of dried powder for all the selected salts. The resultant particle properties emphasized in the present work are the dried particle to initial droplet diameter ratio and the wet basis moisture content. It has been observed that the ratio of mean volume diameter of dried particle to sauter mean diameter of initial droplet lies in the range of 0.4–3.6 meanwhile the wet basis moisture content of dried powder lies in the range of 1.4–3.6 for the selected salts. Artificial neural network (ANN) model is applied for inferring the influence of IHPSD process parameters on the above mentioned dried particle properties and satisfactory convergence with experimental values has been achieved.

Effect of secondary metabolites from several leaf extracts on the green synthesized-ZnO nanoparticles

This study explores a green synthesis approach for zinc oxide nanoparticles (ZnO NPs) using eco-friendly leaf extracts from mango (Mangifera indica), kapok (Ceiba pentandra), and oil palm (Elaeis guineensis Jacq.) trees. The research investigates the effect of the extracts' secondary metabolites on the synthesized ZnO NPs. Qualitative analysis identified the presence of alkaloids, phenols, steroids, and saponins in varying concentrations within each extract. ZnO nanoparticles were successfully synthesized using all three extracts, confirmed by FT-IR spectroscopy with a characteristic Zn–O peak at 416.3 cm−1. XRD analysis revealed the crystalline structure of the nanoparticles, with an additional peak in ZnO_CPLE suggesting potential impurities. SEM images demonstrated the influence of secondary metabolites on particle size and morphology. ZnO_EGLE, containing both phenols and saponins, exhibited the smallest and most uniform nanoparticles (43.3 nm) compared to ZnO_CPLE (94.5 nm) and ZnO_MILE (74.9 nm). TEM analysis further supported these findings, highlighting the crucial role of phenols and saponins as capping agents in controlling particle size and agglomeration. This research suggests a promising green synthesis route for ZnO NPs using these leaf extracts, potentially tailoring particle properties based on the specific secondary metabolite profile.

Morphology characteristics of filler particles and their effects on the low–temperature cracking behavior of asphalt mastics

The article concerned on particle morphology of mineral filler and its impact on mastic cracking property at low temperatures. Limestone and granite fillers with four-sized groups were prepared and further investigated using a simplex-centroid experimental design. The particle morphologies of each filler were captured using a digital image processing. By applying bending beam rheometer tests, mastic cracking behavior was investigated at low temperatures. Results show that compared with granite filler, each limestone filler shows less regular contour shape (except l1), less abundant angularity (except l1, l2, l5 and l17) and surface texture when performed by a simplex-centroid experimental design. The established fractional derivative Burgers model considering creep damage can effectively describe mastic cracking behavior at low temperatures. Composite fractal dimension is the decisively relevant factor with mastic relaxation behavior. Moreover, mastic creep damage is obviously affected by composite morphology characteristics and filler lithology with increasing loading time. All the results are instructive to inform researches of the selection of mineral filler with appropriate particle morphology that will produce asphalt materials with desired performance.

Microstructure evolution during solidification in a low superheat casting process of the Al-Mg2Si composites having excess Si: A phase field study

A two-dimensional phase field (PF) model of solidification during low superheat casting has been developed to grab insight into the microstructure formation mechanism of the Al-xMg2Si-ySi composite, having extra Si as the grain refining agent. The developed PF model employs a seed undercooling based nucleation model to simulate the formation of primary Mg2Si and α-Al grains, wherein the interfacial energy of the Al-melt interface is taken from literature, and a Molecular Dynamics (MD) model is employed to calculate the interfacial energy of the Mg2Si-melt interface. The simulation study predicts the microstructural parameters such as grain size, and sphericity of the primary Al and primary Mg2Si phases, as well identifies the appropriate numerical parameters such as mobility, anisotropy parameters to study the microstructure evolution in the Al-xMg2Si-ySi composites. The kinetics of grain growth of both α-Al and primary Mg2Si have been studied. Novelty of the study lies in developing a near-accurate PF model capable of optimising the weight fraction of Mg2Si and excess Si in the low superheat cast Al-xMg2Si-ySi composite system, in view of obtaining the lower grain size and higher sphericity of both primary Al and primary Mg2Si grains, which is in line with the experimental observations. The proposed PF model is capable of predicting the faceted growth of Mg2Si particles in the Al-xMg2Si-ySi composite, in presence of extra Si and during low superheat casting, and the dendritic growth of Mg2Si in the binary Al-Mg2Si composite having high Mg2Si weight fraction. Following the Jackson’s model of interface growth, it has been demonstrated that the modification of kinetic coefficient leads to a transformation of morphology of Mg2Si particles from large dendritic to faceted ones.

Recent advance for animal-derived polysaccharides in nanomaterials

Inspired by the structure characteristics of natural products, the size and morphology of particles are carefully controlled using a bottom-up approach to construct nanomaterials with specific spatial unit distribution. Animal polysaccharide nanomaterials, such as chitosan and chondroitin sulfate nanomaterials, exhibit excellent biocompatibility, degradability, customizable surface properties, and novel physical and chemical properties. These nanomaterials hold great potential for development in achieving a sustainable bio-economy. This paper provides a summary of the latest research results on the preparation of nanomaterials from animal polysaccharides. The mechanism for preparing nanomaterials through the bottom-up method from different sources of animal polysaccharides is introduced. Furthermore, this paper discusses the potential hazards posed by industrial applications to the environment and human health, as well as the challenges and future prospects associated with using animal polysaccharides in nanomaterials.

A thermogravimetric analysis of residual char formation by gilsonite-filled, polyfurfuryl alcohol composites: acid treatment of gilsonite

Gilsonite (GLS), a natural bitumen containing a considerable amount of asphaltenes, is expected to leave heavy char after pyrolysis; however, its high potential as an efficient filler to enhance the thermal properties of composite materials is surprisingly neglected throughout the literature. On the other hand, polyfurfuryl alcohol (PFA) has attracted much attention as a thermosetting resin due to its excellent char-leaving characteristics, the renewable nature of the monomer(s), and high accessibility at an affordable cost. This study aimed to investigate the thermal stability and char-forming performance of composites made of a PFA resin matrix filled with chemically modified GLS. To modify the ash and sulfur contents of GLS, the nitric acid leaching process was performed according to a D-optimal experimental design approach. The nitric acid concentration (10, 20, and 30 wt.%), treatment time (30, 75, and 120 min), and reaction temperature (30 °C, 50 °C, and 70 °C) were set as the input variables. The morphology (SEM), chemical structure (FTIR), thermal stability (TGA), sulfur content, and ash content of the GLS particles were characterized before and after acid treatment. Thermogravimetric analysis revealed the lowest ash content for GLS after treatment with 10 wt.% acid conc. at 75 °C for 75 min. The nitric acid concentration, reaction temperature, and time were the most influential parameters for improving the ash content of GLS according to their order of appearance. In addition, the inorganic form of sulfur, pyrite, was separated through the acid leaching process. Then, the PFA resin matrix was filled with modified GLS particles at different weight percentages (5, 10, 15, and 20 wt.%) and cured in the presence of an acid catalyst. The thermal stability of the PFA resin was negatively affected by the presence of GLS, probably due to oxidation reactions and disruption of the integrity of the resin structure.

Oxide particles in oxide dispersion strengthened steel neutron-irradiated up to 158 dpa at Joyo

We investigated the stability of oxide nano particles in oxide dispersion-strengthened (ODS) steel, which is a promising candidate material for next-generation reactors, under neutron irradiation at high temperature to high doses. MA957, a 14Cr-ODS steel, was irradiated with Joyo in Japan Atomic Energy Agency under irradiation conditions of 130 dpa at 502 ºC, 154 dpa at 589 ºC, and 158 dpa at 709 ºC. Three-dimensional atom probe (3D-AP) and transmission electron microscope (TEM) observation were performed to characterize the oxide particles in the ODS steels. A high number density of Y-Ti-O particle was observed in the unirradiated and irradiated samples. Almost no change in the morphology of the oxide particles, i.e. average diameter, number density, and chemical composition, has been observed in the samples irradiated to 130 dpa at 502 ºC and to 154 dpa at 589 ºC. A slight decrease in number density was observed in the sample irradiated to 158 dpa at 709 ºC. The hardness of any of the irradiated samples was almost unchanged from that of the unirradiated sample. It was revealed that the oxide particles existed stable, and the strength of the material was sufficiently maintained even after being neutron irradiated to high dose of ∼160 dpa at high temperature up to 700 ºC.

Enhancing Anticancer Potential: Optimization of Allicin Extraction from Regular Garlic and Characterization of Allicin-Loaded Copper Oxide Nanoparticles

This research aimed to optimize the extraction and purification processes of allicin from regular garlic (Allium sativum) and to evaluate the potential of allicin-loaded copper oxide (CuO) nanoparticles for anticancer applications. Initially, various solvents, including MilliQ water, 25% methanol, and phosphate buffer pH 2.5 in 60% methanol, were tested to determine the most effective conditions for extracting allicin. Among these, MilliQ water and 25% methanol demonstrated the highest extraction efficiencies, as evidenced by their absorbance values. The extracted allicin underwent purification and was subsequently characterized using fourier-transform infrared spectroscopy (FTIR) and high-performance liquid chromatography (HPLC). These techniques confirmed the identity and high purity of the allicin. Following purification, the allicin was encapsulated into copper oxide (CuO) nanoparticles using an optimized nanoprecipitation protocol. The physicochemical properties of the allicin-loaded nanoparticles were thoroughly characterized. Dynamic light scattering (DLS) analysis revealed a mean particle size of 123 nm, indicating a uniform and nanoscale particle distribution. Zeta potential measurements indicated a surface charge of -28.34 mV, suggesting good stability of the nanoparticles in suspension. Scanning electron microscopy (SEM) was employed to further analyze the particle size, surface charge, and morphology, providing detailed insights into the structural attributes of the nanoparticles. The successful encapsulation of allicin into CuO nanoparticles not only enhances the stability and bioavailability of allicin but also leverages the unique properties of CuO nanoparticles, which are known for their anticancer, antioxidant, and antimicrobial activities. This study underscores the potential of allicin-loaded CuO nanoparticles derived from regular garlic as a promising formulation for pharmaceutical applications, particularly in the field of oncology. These findings warrant further investigation into their clinical efficacy and safety to fully harness their therapeutic potential.

Encapsulation of Arthrospira platensis polyphenolic extract using supercritical emulsion-based process

Arthrospira platensis polyphenolic natural extracts have several benefits for human health. Due to their instability and reduced shelf-life, these extracts are usually encapsulated. This work analyzed the supercritical emulsion extraction (SEE) process for the production of polymeric nanoparticles loaded with A. platensis polyphenolic extracts. The objective of this work was to evaluate a powdered encapsulation system to overcome the drawbacks of liquid systems, which are those mainly used for microalgae extract stabilization. An optimization study was performed investigating different process parameters and comparing the obtained particles in terms of particle size distribution, morphology, and encapsulation efficiency. The process permitted the successfull production of loaded polymeric nanoparticles with an encapsulation efficiency up to 74 % in the best operating conditions. The SEE process allowed a better control of morphology and particle size distribution of the nanometric particles operating in a continuous mode.

Enhancing flowability of lamivudine through quasi-emulsion solvent-diffusion (QESD) crystallization: A comprehensive study on surfactant impact, particle morphology by QbD concepts and tablet compression challenges

Lamivudine (LMD), an enantiomer of 2′-deoxy-3′-thiacytidine, plays a crucial role in combatting HIV-1 and managing hepatitis B virus infections. Despite its effectiveness, challenges arise from its difficult flowability and tendency to agglomerate during storage, necessitating a granulation step before tablet compression, as direct compression has proven ineffective. This study aimed to optimize Lamivudine spherical agglomerates using response surface methodology, delving into the intricate relationship between design factors (concentration of tween, span, and acetone) and experimental outcomes (yield and particle size) through central composite design. Analysis of variance (ANOVA) was employed for optimization, with the Quasi-emulsion solvent-diffusion (QESD) crystallization technique utilized for the checkpoint batch. This technique, involving a single solvent and antisolvent with surfactants, showcased remarkable enhancements in flowability and reduced storage agglomeration. The impact of various surfactants [Hydroxy Propyl Methyl Cellulose (HPMC), polysorbate 80, and sorbitane monooleate] on particle morphology, flowability, and storage agglomeration during crystallization was thoroughly assessed. While achieving direct compression into tablets, the porous structure of LMD agglomerates presented challenges in tablet press production speeds, prompting adjustments such as reducing punch speed or implementing a precompression step. Positive outcomes were realized for disintegration and in vitro drug release in comparison to direct compression and wet granulation methods. In conclusion, the QESD crystallization technique successfully yielded hollow, spherical LMD agglomerates with enhanced properties, representing a significant milestone in pharmaceutical formulation.

The effects of adding Si3N4 as a nitrogen source on the properties of Ni-Free Co-28Cr-6Mo-xN alloy powders developed by mechanical alloying

Co-Cr-Mo alloys, which also contain Ni, are often used as materials for implants in orthopedic surgery due to their excellent mechanical properties and resistance to corrosion. However, when these alloys are implanted into the body, they can release nickel ions into the host tissues, which can pose health risks over time. To address this issue, nitrogen can be substituted for nickel. This study involves the synthesis of cobalt-based alloy powders, following the chemical composition specified by ASTM F1537, using different percentages of silicon nitride as a nitrogen source via the mechanical alloying method in an argon atmosphere. The effects of increasing silicon nitride content on the particle morphology, particle size, phase transformations, microstructure, and hardness of the synthesized powders were investigated using XRD, SEM, TEM, and microhardness tests. The results obtained from the X-ray diffraction analysis indicate that the alloying process was conducted effectively. It was observed that the silicon nitride underwent decomposition, and a portion of its nitrogen reacted with chromium to form the chromium nitride phase. Additionally, it was observed that an increase in the silicon nitride content resulted in a decrease in crystallite size and an increase in lattice strain. Adding silicon nitride in varying percentages resulted in crystal sizes within the nanometer range. The SEM results indicated that the size of powder particles decreased with an increase in the content of silicon nitride, and there was a more uniform distribution of particle sizes, with less variation in size. The TEM images showed that all percentages of silicon nitride resulted in a fine-grained polycrystalline phase, where the size of the crystallites decreased with an increase in the amount of silicon nitride. The corresponding SAED patterns supported this observation. Moreover, the hardness of the material increased as the silicon nitride content increased.

The Influence of Heat Treatment on the Microstructure and Properties of a Cu-Bearing Ultra-Low Carbon Steel.

This study reveals the relationship between the Cu precipitates and mechanical properties of a Cu-baring ultra-low carbon steel after two-phase zone quenching and tempering at 923 K for 0.5-2.5 h. The tensile and microstructural properties were investigated as a function of heat treatment time. The contribution of the precipitation-strengthening mechanism to yield strength was calculated. The size, morphology, and distribution of the precipitated particles were observed using TEM. As the heat treatment time increased, the strength gradually decreased and then remained stable, and the elongation gradually increased and then remained stable. Additionally, the contributions of each strengthening mechanism to the yield strength under different heat treatments were 117, 107, 102, and 89 MPa, respectively. The size and quantity of the precipitates increased with the increase in heat treatment time. After tempering for more than 2 h, the precipitates continued to coarsen, but their quantity decreased. The precipitated Cu had a 3R structure with a length of approximately 17.1 nm and a width of approximately 9.7 nm, with no twinning inside. The stacking order was ABC/ABC. The stable Cu precipitation structure was FCC, maintaining a K-S orientation relationship 11¯1FCC Cu //(0 1 1) α, 1¯10FCC Cu//[11¯1] α.

Three nonconventional starch: Comparison of physicochemical properties and in vitro digestibility.

Extraction of starch from waste is also an effective way to recover resources and provide new sources of starch. In this study, starch was isolated from white kidney bean residue, chickpea residue, and tiger nut meal after protein or oil extraction, and the morphology of starch particles was observed to determine their physicochemical properties and in vitro digestibility. All these isolated starches had unique properties, among which white kidney bean starch (KBS) had a high amylose content (43.48%), and its structure was better ordered. Scanning electron microscopy revealed distinct granular morphologies for the three starches. KBS and chickpea starch (CHS) were medium-granular starches, whereas tiger nut starch was a small granular starch. Fourier transform infrared spectroscopy analysis confirmed the absence of significant differences in functional groups and chemical bonds among the three starch molecules. In vitro digestibility studies showed that CHS is more resistant to enzymatic degradation. Overall, these results will facilitate the development of products based on the separation of nonconventional starches from waste.

Ni Particle Morphology and Support Effect in the Catalytic Decomposition of Methane: Into the Design of Novel, High Yield Catalyst for Catalytic Decomposition of Methane

Ni Particle Morphology and Support Effect in the Catalytic Decomposition of Methane: Into the Design of Novel, High Yield Catalyst for Catalytic Decomposition of Methane