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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 541 records · Page 30
All sourcesNASA NTRSDOE OSTI
DOE OSTI2014

Hydrothermal synthesis, characterization and up/down-conversion luminescence of barium rare earth fluoride nanocrystals

Graphical abstract: Lanthanide ions doped bare earth rare earth fluoride nanocrystals are synthesized by hydrothermal technology and characterized. The down/up-conversion luminescence of them are discussed. - Highlights: • Mixed hydrothermal system H{sub 2}O–OA (EDA)–O-A(LO-A) is used for synthesis. • Barium rare earth fluoride nanocrystals are synthesized comprehensively. • Luminescence for down-conversion and up-conversion are obtained for these systems. - Abstract: Mixed hydrothermal system H{sub 2}O–OA (EDA)–O-A(LO-A) is developed to synthesize barium rare earth fluorides nanocrystals (OA = oleylamine, EDA = ethylenediamine, O-A = oleic acid and LO-A = linoleic acid). They are presented as BaREF{sub 5} (RE = Ce, Pr, Nd, Eu, Gd, Tb, Dy, Y, Tm, Lu) and Ba{sub 2}REF{sub 7} (RE = La, Sm, Ho, Er, Yb). The influence of reaction parameters (rare earth species, hydrothermal system and temperature) is checked on the phase and shape evolution of the fluoride nanocrystals. It is found that reaction time and temperature of these nanocrystals using EDA (180 °C, 6 h) is lower than those of them using OA (220 °C, 10 h). The photoluminescence properties of these fluorides activated by some rare earth ions (Nd{sup 3+}, Eu{sup 3+}, Tb{sup 3+}) are studied, and especially up-conversion luminescence of the four fluoride nanocrystal systems (Ba{sub 2}LaF{sub 7}:Yb, Tm(Er), Ba{sub 2}REF{sub 7}:Yb, Tm(Er) (RE = Gd, Y, Lu)) is observed.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Carbonated hydroxyapatite starting from calcite and different orthophosphates under moderate hydrothermal conditions: Synthesis and surface reactivity in simulated body fluid

Highlights: • Carbonated apatite (CAP) could be easily obtained from CaCO{sub 3} and orthophosphates. • Highest CaCO{sub 3} dissolution and apatitic carbonate content were obtained with H{sub 3}PO{sub 4}. • A-B-type CAP was formed. • The synthesized CAP was thermally stable up to 1000 °C. • This CAP showed high biomineralization activity before and after thermal treatment. - Abstract: The one-step synthesis of carbonated hydroxyapatite (CAP) using calcite and different orthophosphates was investigated in a closed batch reactor. Only orthophosphoric acid could lead to the complete decomposition of calcite particles, when the reaction temperature was set at 80 °C. On the other hand, the reaction time and the dilution of the initial calcite suspension had no significant influence on the formation of the solid products. CAP was formed as the main crystalline calcium phosphate with the carbonate content in the range of 4.2–4.6 wt.%. The thermal decarbonation of the synthesized CAP started at 750 °C but it was only significant at 1000 °C under air atmosphere. This thermal decarbonation was total at 1200 °C or above. All CAP samples and products following thermal treatments were found bioactive in the test using simulated body fluid (SBF) solution.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Ionic liquid-assisted preparation of square-shaped Y{sub 2}O{sub 3} nanoplates

Highlights: • Y{sub 4}O(OH){sub 9}(NO{sub 3}) nanosheets were prepared by an ionic liquid-assisted mixed solvothermal route. • Y{sub 2}O{sub 3} nanosheets were obtained after calcining the Y{sub 4}O(OH){sub 9}(NO{sub 3}) nanosheets. • The Y{sub 2}O{sub 3} nanosheets are with length of about 300 nm and thickness of several nanometers. - Abstract: Uniform square-shaped Y{sub 4}O(OH){sub 9}(NO{sub 3}) nanoplates with side length of about 300 nm and thickness of tens of nanometers have been successfully prepared by an ionic liquid-assisted mixed solvothermal route. Y{sub 2}O{sub 3} nanoplates with similar size were obtained after calcining the Y{sub 4}O(OH){sub 9}(NO{sub 3}) nanoplates at 800 °C. The products were analyzed by powder X-ray diffraction (XRD), thermogravimetric analysis (TG), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high resolution TEM (HRTEM), and electron diffraction (ED). The effects of reaction time, composition of solvents, and the molar ratio of reagents on the morphology of the products have been investigated. The possible formation mechanism of the Y{sub 4}O(OH){sub 9}(NO{sub 3}) nanoplates was also discussed. Y{sub 2}O{sub 3}:Eu{sup 3+} nanoplates were also synthesized and their photoluminescent properties were examined.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Wide emission-tunable CdTeSe/ZnSe/ZnS core–shell quantum dots and their conjugation with E. coli O-157

Highlights: • QDs with variety morphology were obtained via an injection controlled process. • 3-D PL spectra of core–shell QDs show different excitation wavelength dependence. • The PL intensity of QDs with ZnSe transition layer increases dramatically. • Core–shell QDs were processed into aqueous phase and conjugated with E. coli O-157. - Abstract: Wide emission-tunable and different morphological alloyed CdTeSe quantum dots (QDs), CdTeSe/ZnS and CdTeSe/ZnSe/ZnS core–shell QDs were successfully synthesized via an injection controlled process. The effect of injection procedure and reaction temperature were systematically discussed and the growth mechanism was proposed. Most efficient PL wavelength was correlated with reaction time and temperature. The 3-D PL spectra of spherical bare CdTeSe and core–shell QDs with different passivation showed different excitation wavelength dependency. The PL intensity of CdTeSe/ZnSe/ZnS core–shell QDs increased greatly in comparison with that of CdTeSe and CdTeSe/ZnSe QDs. ZnSe transition layer played an important role in improving the PL intensity by providing a smoothened interface and gradient band offsets. The core–shell QDs were transferred into aqueous phase and successfully conjugated with Escherichia coli O-157. The proposed phase-transfer and bio-labeling strategy may be applicable to various QDs with different compositions.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2015

A study of thermal properties of sodium titanate nanotubes synthesized by microwave-assisted hydrothermal method

Highlights: • The microwave-assisted hydrothermal route was used for titanate nanotubes synthesis. • Conversion to single-phase nanotube morphology completes after 8 h reaction time. • The nanotube morphology is stable up to 600 °C, as determined by in-situ XRD and SEM. • Sodium ions migrate to the surface due to thermal motion and structure condensation. - Abstract: Sodium titanate nanotubes (NaTiNTs) were synthesized by microwave-assisted hydrothermal treatment of commercial TiO{sub 2}, at constant temperature (135 °C) and different irradiation times (15 min, 1, 4, 8 and 16 h). The products were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, differential scanning calorimetry and specific surface area measurements. The irradiation time turned out to be the key parameter for morphological control of the material. Nanotubes were observed already after 15 min of microwave irradiation. The analyses of the products irradiated for 8 and 16 h confirm the complete transformation of the starting TiO{sub 2} powder to NaTiNTs. The nanotubes are open ended with multi-wall structures, with the average outer diameter of 8 nm and specific surface area up to 210 m{sup 2}/g. The morphology, surface area and crystal structure of the sodium titanate nanotubes synthesized by microwave-assisted hydrothermal method were similar to those obtained by conventional hydrothermal method.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2016

Three-dimensional flowerlike iron oxide nanostructures: Morphology, composition and metal ion removal capability

Graphical abstract: The iron alkoxide precursors are calcined into α-Fe{sub 2}O{sub 3}, Fe{sub 3}O{sub 4} microstructures with different morphologies by changing calcination atmosphere, reaction time of precursors and calcination temperature simply. The Fe{sub 2}O{sub 3}/Ag hybrid composites prepared through aqueous synthesis and light irradiation. - Highlights: • α-Fe{sub 2}O{sub 3} and Fe{sub 3}O{sub 4} microstructures with different morphologies were created. • Solvents play an important role for the solvothermal treatment of precursors. • The α-Fe{sub 2}O{sub 3} microstructures show excellent adsorption properties. • Fe{sub 2}O{sub 3}/Ag hybrid composites were prepared to improve their properties. - Abstract: The flower-like precursors of Fe alkoxide constructed by the self-assembly of nanoflakes were prepared. Time-dependent experiments confirmed the formation mechanism of flower-like precursors. After calcination, α-Fe{sub 2}O{sub 3} and Fe{sub 3}O{sub 4} nanostructures with different morphologies were created. Fe{sub 3}O{sub 4} nanostructures containing blocks with a truncated octahedron structure were obtained under N{sub 2} protection. α-Fe{sub 2}O{sub 3} nanostructures were prepared in an air atmosphere. The values of maximum adsorption capacity of α-Fe{sub 2}O{sub 3} nanostructures for Cr{sup 6+} ions were much higher than that of commercial bulk α-Fe{sub 2}O{sub 3}. Ag NPs were deposited on α-Fe{sub 2}O{sub 3} nanostructures through an aqueous synthesis and light irradiation using L-cysteine as a linker. Such procedure is utilizable for the preparation of the composites of noble metals and magnetic materials.

36 MATERIALS SCIENCE↗
DOE OSTI2016

Phenoxo bridged dinuclear Zn(II) Schiff base complex as new precursor for preparation zinc oxide nanoparticles: Synthesis, characterization, crystal structures and photoluminescence studies

Highlights: • A novel nano-scale Zn(II) complex was synthesized by solvothermal method. • Chemical structure of the nanostructures was characterized as well as bulk complex. • The photoluminescence property of the complex was investigated at room temperature. • The thermogravimetry and differential thermal analysis were carried out. • Thermal decomposition of the nanostructures was prepared zinc oxide nanoparticles. - Abstract: Nanoparticles of a novel Zn(II) Schiff base complex, [Zn(HL)NO{sub 3}]{sub 2} (1), (H{sub 2}L = 2-[(2-hydroxy-propylimino) methyl] phenol), was synthesized by using solvothermal method. Shape, morphology and chemical structure of the synthesized nanoparticles were characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), Fourier Transform Infrared Spectoscopy (FT-IR) and UV–vis spectroscopy. Structural determination of compound 1 was determined by single-crystal X-ray diffraction. The results were revealed that the zinc complex is a centrosymmetric dimer in which deprotonated phenolates bridge the two five-coordinate metal atoms and link the two halves of the dimer. The thermal stability of compound 1 was analyzed by thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC). The effect of the initial substrates concentration and reaction time on size and morphology of compound 1 nanostructure was investigated as well. Furthermore, the luminescent properties of the complex 1 were examined. ZnO nanoparticles with diameter between 15 and 20 nm were simply synthesized by solid-state transformation of compound 1 at 700 °C.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Plasmonic Ag/Ag2O nanoparticles anchored needle-like Bi2O3 as an efficient visible-light-driven nanocomposite photocatalyst

Highlights: • Deposition of plasmonic Ag/Ag{sub 2}O NPs on the surface of Bi{sub 2}O{sub 3}. • Synthesis of Ag/Ag{sub 2}O@Bi{sub 2}O{sub 3} by thermal-assisted precipitation. • SPR of Ag enhances use of solar energy and transfer of carriers. • Degradation of Reactive Black 5 by CCD model. - Abstract: In this study, a thermal-assisted precipitation method was applied for the uniform deposition of plasmonic Ag/Ag{sub 2}O nanoparticles on the surface of needle-like Bi{sub 2}O{sub 3} to synthesis Ag/Ag{sub 2}O@Bi{sub 2}O{sub 3} nanocomposite. The synthesized nanocomposite was characterized by different techniques including UV–vis spectrophotometry, X-ray diffraction (XRD), scanning electronic microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray mapping, and photoluminescence (PL). The visible-light-driven photocatalytic activities of Ag{sub 2}O@Bi{sub 2}O{sub 3} and Ag/Ag{sub 2}O@Bi{sub 2}O{sub 3} were evaluated on photo-degradation of Reactive Black 5 (RB 5) dye as model pollutant. The effect of process variables including the initial dye concentration, reaction time, and pH on the photo-degradation of RB 5 was studied by Central Composite Design (CCD) methodology. It was found that the photo-degradation rate of Ag/Ag{sub 2}O@Bi{sub 2}O{sub 3} was higher than that of the Ag{sub 2}O@Bi{sub 2}O{sub 3} and Bi{sub 2}O{sub 3}. The highly efficient photocatalytic activity of Ag/Ag{sub 2}O@Bi{sub 2}O{sub 3} nanocomposite is mainly ascribed to enhancing photogenerated electron-hole separation and the surface plasmon resonance (SPR) influence of silver-based nanoparticles.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Fast synthesis of sub-10 nm β-NaYF4:Yb3+, Er3+@NaYF4 core-shell upconversion nanocrystals mediated by oleate ligands

Highlights: • Fast synthesize ultra-small β-NaYF{sub 4}:Yb{sup 3+}, Er{sup 3+} UCNCs with 0 min reaction or down to 5.3 nm. • Highly bright sub-10 nm β-NaYF{sub 4}:Yb{sup 3+}, Er{sup 3+} core-shell NCs were obtained. • OA{sup −} ligands cannot only promote the α-to-β phase transition, but also inhibit the crystal growth. • OA{sup −} ligands manipulated phase transition and size evaluation is also applicable to other UCNCs. - Abstract: We developed a facile approach for the fast synthesis of ultrasmall and monodisperse β-NaYF{sub 4}:Yb{sup 3+}, Er{sup 3+} nanocrystals down to 5.3 nm with the assistant of oleate ligands, based on which the highly bright sub-10 nm β-NaYF{sub 4}:Yb{sup 3+}, Er{sup 3+}@NaYF{sub 4} core-shell nanocrystals with three order of magnitude increased upconversion emission were successfully obtained by a seed-mediated growth method. The reaction time and temperature dependent experimental results implied that the introduciton of extra oleate ligands can both promote the α-to-β phase transition and impeded the crystal growth of NaYF{sub 4}, which is due to the oleate ligand induced orderly arrangement of Y{sup 3+} and capping effect, respectively. It is expected that the oleate ligands mediated phase transition and size evaluation, demonstrated here in NaYF{sub 4}:Yb{sup 3+}, Er{sup 3+} NCs, is also applicable to other lanthanide-doped upconversion nanocrystals.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Size controlled synthesis of SnO2 and its electrostatic self- assembly over reduced graphene oxide for photocatalyst and supercapacitor application

Highlights: • The influence of pH, reaction time and temperature over the control of size of the spheres of SnO{sub 2} by hydrothermal method and further assembly over reduced graphene oxide has been carried out in this report. • The modification of SnO{sub 2} via (3- amino propyl triethoxysilane) makes the electrostatic self- assembly between the positively charged SnO{sub 2} nanostructure and the negatively charged graphene oxide (GO). • The impacts of concentration of GO added to SnO{sub 2} nanostructures and its significance on the morphology and the capacitive property of SnO{sub 2}/rGO composite are evaluated. • The functionalization of graphene enhances the capacitance as well as provides anchoring sites for the decoration by metal oxide nanostructures. - Abstract: Hydrothermally-synthesized, size and shape-controlled SnO{sub 2} nanospheres were electrostatically self-assembled over the surface of reduced graphene oxide (rGO). The control over decoration of SnO{sub 2} nanospheres on rGO was studied by microscopic analysis and the crystallographic structure of SnO{sub 2} hybrid nanocomposites (SnO{sub 2}: rGO) was determined from X-Ray diffraction analysis (XRD). Hybrid nanocomposite in 1:3 ratio exhibited (i) excellent methylene blue degradation capability within 3 min under visible light condition and (ii) high specific capacitance of 337.52 F/g at 0.5 A/g in 1 M H{sub 2}SO{sub 4} electrolyte with 89% of retention after 5000 cycles.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2015

Preparation and CO 2 adsorption properties of soft-templated mesoporous carbons derived from chestnut tannin precursors

This paper presents a soft templating approach for mesoporous carbon using the polyphenolic heterogeneous biomass, chestnut tannin, as the carbon precursor. By varying synthesis parameters such as tannin:surfactant ratio, cross-linker, reaction time and acid catalyst, the pore structure could be controllably modulated from lamellar to a more ordered hexagonal array. Carbonization at 600 °C under nitrogen produced a bimodal micro-mesoporous carbonaceous material exhibiting enhanced hydrogen bonding with the soft template, similar to that shown by soft-templating of phenolic-formaldehyde resins, allowing for a tailorable pore size. By utilizing the acidic nature of chestnut tannin (i.e. gallic and ellagic acid), hexagonal-type mesostructures were formed without the use of an acid catalyst. The porous carbon materials were activated with ammonia to increase the available surface area and incorporate nitrogen-containing functionality which led to a maximum CO 2 adsorption capacity at 1 bar of 3.44 mmol/g and 2.27 mmol/g at 0 °C and 25 °C, respectively. The ammonia-activated carbon exhibited multiple peaks in the adsorption energy distribution which indicates heterogeneity of adsorption sites for CO 2 capture.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Structure-dependent performance of TiO 2 /C as anode material for Na-ion batteries

The performance of energy storage materials is highly dependent on their nanostructures. Herein, hierarchical rod-in-tube TiO 2 with a uniform carbon coating is synthesized as the anode material for sodium-ion batteries by a facile solvothermal method. This unique structure consists of a tunable nanorod core, interstitial hollow spaces, and a functional nanotube shell assembled from two-dimensional nanosheets. By adjusting the types of solvents used and reaction time, the morphologies of TiO 2 /C composites can be tuned to nanoparticles, microrods, rod-in-tube structures, or microtubes. Among these materials, rod-in-tube TiO 2 with a uniform carbon coating shows the highest electronic conductivity, specific surface area (336.4 m 2 g -1 ), and porosity, and these factors lead to the best sodium storage capability. Benefiting from the unique structural features and improved electronic/ionic conductivity, the as-obtained rod-in-tube TiO 2 /C in coin cell tests exhibits a high discharge capacity of 277.5 and 153.9 mAh g -1 at 50 and 5000 mA g -1 , respectively, and almost 100% capacity retention over 14,000 cycles at 5000 mA g -1 . In operando high-energy X-ray diffraction further confirms the stable crystal structure of the rod-in-tube TiO 2 /C during Na + insertion/extraction. Finally, this work highlights that nanostructure design is an effective strategy to achieve advanced energy storage materials.

25 ENERGY STORAGE↗
DOE OSTI2015

Application of active quenching of second generation wire for current limiting

Superconducting fault current limiters (SFCL's) are increasingly implemented in the power grid as a protection of substation equipment from fault currents. Resistive SFCL's are compact and light, however they are passively triggered and thus may not be sufficiently sensitive to respond to faults in the distribution grid. Here, we explore the prospect of adding an active management feature to a traditional resistive SFCL. A flexible radio-frequency coil, which is an integral part of the switching structure, acts as a triggering device. We show that the application of a short, 10 ms, burst of ac magnetic field during the fault triggers a uniform quench of the wire and significantly reduces the reaction time of the wire at low currents. The ac field burst generates a high density of normal zones, which merge into a continuous resistive region at a rate much faster than that of sparse normal zones created by the transport current alone.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2026

Engineering acid-base active sites on an N-doped biochar catalyst for microwave-assisted biodiesel production from waste cooking oil

Acid-base bifunctional catalysts play a crucial role in converting high-free fatty acid (FFA) feedstocks into biodiesel by enabling the simultaneous esterification and transesterification of triglycerides in a single step, thereby minimizing saponification and streamlining the process. In this study, we report the design and development of a novel N-doped acid-base bifunctional biochar catalyst synthesized from renewable biomass precursors- glucose and chitosan. The catalyst’s acidic sites were introduced via surface functionalization with o-sulfobenzoic acid cyclic anhydride, grafting -SO₃H groups onto the carbon framework, while basic sites were generated from amine functionalities (-NH) derived from chitosan, yielding a robust and truly bifunctional surface. The catalyst was characterized and used for the microwave-assisted transesterification of waste cooking oil, and process optimization using response surface methodology (RSM-CCD) yielding a maximum biodiesel yield of 98.8 ± 0.4% under optimal conditions (methanol-to-oil molar ratio 20:1, catalyst loading 5.7 wt%, temperature 99 °C, and reaction time 46.6 min). The catalyst demonstrated good stability, maintaining a yield of 92.2 ± 0.4% after eight reuse cycles. A Life Cycle Assessment (LCA) conducted for 1 kg of biodiesel production revealed a global warming potential of 0.85 kg CO 2 eq and human toxicity potential of 1.59 kg 1,4-DB eq, with the largest environmental contributions arising from catalyst preparation and reuse. In conclusion, this work highlights a green and circular approach to biodiesel production, combining renewable catalyst design, waste feedstock utilization, and quantitative sustainability assessment to guide future developments in sustainable catalysis and biofuel engineering.

Bifunctional catalyst↗
DOE OSTI2021

New concept of radiolytic synthesis of gold nanoparticles in continuous flow

Radiolytic synthesis has been used to produce a plethora of unsupported and supported metallic nanoparticles in batch. As proof of a new concept, we evaluated the formation of gold nanoparticles by radiolytic synthesis in continuous flow using a millifluidic reactor. A mixture of gold ions solution, branched polyethyleneimine, and ethylene glycol yielded gold nanoparticles with a mean size of 3.4 ± 1.0 nm after irradiation with an X-ray irradiator (127 Gy/min) at an absorbed dose of 5.1 kGy. The morphology and size distribution of gold nanoparticles was influenced by AgNO 3 , where its absence resulted in a mean size of 20.9 ± 15.8 nm. The radiolytic synthesis of gold nanoparticles in continuous flow was achieved in short reaction times (<60 min), at room temperature, and with low concentrations of both stabilizing and reducing agents. Furthermore, these results demonstrate the potential of radiolytic synthesis in continuous flow for high-throughput formation of metallic nanoparticles with controlled specifications in size and distribution.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2015

Synthesis and characterization of carboxymethyl cellulose from office waste paper: A greener approach towards waste management

Highlights: • Carboxymethyl cellulose (CMC) was successfully prepared from waste paper. • CMC had maximum degree of substitution (DS) 1.07. • Rheological studies of CMC (DS, 1.07) showed non-Newtonian pseudoplastic behavior. • Characterization of CMC was done by FT-IR and NMR techniques. • Morphology of prepared CMC was studied by SEM. - Abstract: In the present study, functionalization of mixed office waste (MOW) paper has been carried out to synthesize carboxymethyl cellulose, a most widely used product for various applications. MOW was pulped and deinked prior to carboxymethylation. The deinked pulp yield was 80.62 ± 2.0% with 72.30 ± 1.50% deinkability factor. The deinked pulp was converted to CMC by alkalization followed by etherification using NaOH and ClCH{sub 2}COONa respectively, in an alcoholic medium. Maximum degree of substitution (DS) (1.07) of prepared CMC was achieved at 50 °C with 0.094 M and 0.108 M concentrations of NaOH and ClCH{sub 2}COONa respectively for 3 h reaction time. The rheological characteristics of 1–3% aqueous solution of optimized CMC product showed the non-Newtonian pseudoplastic behavior. Fourier transform infra red (FTIR), nuclear magnetic resonance (NMR) and scanning electron microscope (SEM) study were used to characterize the CMC product.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2017

Nano-carbons from waste tyre rubber: An insight into structure and morphology

Highlights: • Synthesis of carbon nanoparticles (CNPs) from waste tyre rubber (WTR). • High temperature approach. • Nano-spherical carbons (diameters: 30-40 nm, specific surface area: 117.7 m{sup 2}/g). - Abstract: This study reports on the novel and sustainable synthesis of high value carbon nanoparticles (CNPs) from waste tyre rubber (WTR), using an innovative high temperature approach. As waste tyres are composed, primarily, of carbon – accounting for some 81.2 wt% – they represent a promising source of carbon for many potential applications. However, cost-effective options for their processing are limited and, consequently, billions of waste tyres have accumulated in landfills and stockpiles, posing a serious global environmental threat. The rapid, high temperature transformation of low value WTR to produce valuable CNPs, reported here, addresses this challenge. In this study, the transformation of WTRs was carried out at 1550 °C over different reaction times (5 s to 20 min). The structure and morphology of the resulting CNPs were investigated using X-ray diffraction (XRD), Raman spectroscopy, X-ray photon spectroscopy (XPS), N{sub 2} isothermal adsorption method and scanning electron microscopy (SEM). The formation of CNPs with diameters of 30 and 40 nm was confirmed by Field Emission Electron Microscopy (FE-SEM). Longer heating times also resulted in CNPs with regular and uniform spherical shapes and a specific surface area of up to 117.7 m{sup 2}/g, after 20 min. A mechanism that describes the formation of CNPs through mesophase nuclei intermediate is suggested.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗