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At least 1,333 records · Page 74

Enhancement of hard magnetism and chemical order of synthetic L 1 0 -FeNi

An ordered tetragonal L 1 0 -FeNi, also known as meteoritic mineral tetrataenite – a promising rare-earth-free hard-magnetic compound – has been synthesized starting from a mechanochemically-activated disordered cubic A1-FeNi via formation of a chemically-ordered FeNiN intermediate and its subsequent denitrogenation and further purification of the product. The nature of a process control agent employed during the mechanochemical activation of A1-FeNi and ammonia flow velocity during the synthesis of the intermediate are two of the main factors controlling the nitrogenation. Denitrogenation with hydrogen at elevated pressures and at temperatures substantially below the order-disorder L 1 0 -FeNi → A1-FeNi transition preserves the chemical order established in the intermediate nitride. Further, post-synthesis refinement of the L 1 0 -FeNi product includes the removal of residual nitrides with a dilute acid to further improve hard-magnetic properties of the material. The L 1 0 -FeNi powders synthesized using this method exhibit a coercivity as high as 2.3 kOe and a maximum energy product reaching 6 MGOe – the highest values ever reported for a synthetic tetrataenite.

36 MATERIALS SCIENCE↗

A split luciferase system for studying coronavirus Mpro dimerization in vitro and in living cells

The main protease enzyme (Mpro) of coronaviruses cleaves the viral polyprotein into functional units essential for virus replication. Prior work has demonstrated that Mpro functions as a homodimer. However, studies on the mechanism of dimerization have been challenging because the purified protease is mostly dimeric, dimerization-defective mutants lack proteolytic activity, and robust cell-based assays have yet to be reported. To enable work on Mpro dimerization, we have developed a quantitative luciferase-based SARS-CoV-2 (SARS2) Mpro biosensor that accurately reports protein dimerization in living cells and, upon purification, also in vitro. Co-transfection of cells with a construct expressing Mpro fused to the 18 kDa LargeBiT of luciferase (LgBiT) and a second construct with Mpro fused to the 1 kDa SmallBiT of luciferase (SmBiT) results in a reconstitution of luciferase activity in a dose-dependent manner that requires conserved residues within the dimerization interface. Proteolytic activity is dispensable for dimerization and, uniquely, a C145A catalytically inactive mutant exhibits enhanced dimerization signal likely due to lower cytotoxicity. Mpro enzymes from multiple different coronaviruses also dimerize in this system, indicating mechanistic conservation. Interestingly, this dimerization biosensor also provides a quantitative read-out of inhibitor-facilitated dimerization. Covalent SARS2 Mpro inhibitors such as nirmatrelvir cause a 3- to 5-fold increase in luciferase activity. Together with corroborating structural, biophysical, and molecular dynamics experiments, our studies support a model in which covalent Mpro inhibitors such as nirmatrelvir simultaneously block catalytic activity and induce allosteric stabilization of the dimeric complex.

SARS-CoV-2 main protease (Mpro/3CLpro)↗

The HypA and HypB metallochaperones from Methanococcus maripaludis have unique metal-binding properties and a distinct nickel transfer mechanism

[NiFe] hydrogenases are widespread microbial metalloenzymes that catalyze the reversible conversion of hydrogen (H2) to protons and electrons, playing key roles in energy metabolism. The biosynthesis of the NiFe(CN) 2 CO cofactor involves a suite of maturation proteins, including the HypA and HypB nickel metallochaperones. Here, we define the metal-binding properties, nucleotide-dependent behavior, and functional interplay of HypA and HypB from the hydrogenotrophic methanogenic archaeon, Methanococcus maripaludis . Methanogens have multiple essential nickel-dependent enzymes, so they require efficient systems for nickel delivery that remain largely unexplored. Purified M. maripaludis HypA binds zinc or mononuclear iron at the C-terminal metal binding site, the latter of which has not been reported in other HypA proteins and may serve a unique regulatory role in methanogens. The G-protein metallochaperone HypB binds nickel at the G-domain, which stimulates GTPase activity. Size exclusion chromatography experiments reveal that HypA and HypB form complexes in the presence of nickel, and zinc-bound HypA is optimized for nickel transfer from HypB. The identity of the nucleotide bound to HypB (GDP or GTP) alters the oligomeric state of HypA-HypB complexes, supporting a GTPase-mediated nickel delivery pathway. The HypA-HypB 2 complex configuration is enriched and stable in the presence of GDP and nickel, indicating that this complex delivers nickel to the hydrogenase as opposed to HypA alone. Interestingly, affinity purification-mass spectrometry revealed that HypB interacts with several nickel-dependent proteins, suggesting that HypB may play a broader role in nickel homeostasis in M. maripaludis . Together, this work establishes a biochemical framework for HypAB-mediated nickel trafficking in methanogens.

[NiFe] hydrogenase↗

Evaluation of β-galactosidase from Lactobacillus acidophilus as biocatalyst for galacto-oligosaccharides synthesis: Product structural characterization and enzyme immobilization

β-Galactosidase is an important industrial enzyme that catalyzes reaction of lactose hydrolysis and recently more interesting reaction of transgalactosylation, yielding a highly valuable group of prebiotic compounds named galacto-oligosaccharides (GOS). In this paper, parameters for achieving high yields of tailor-made GOS using crude β-galactosidase obtained from Lactobacillus acidophilus ATCC 4356, probiotic bacteria regarded as safe for human consumption, were optimized. At the same time, detailed structural elucidation of obtained GOS was conducted, and it was concluded that β-galactosidase from L. acidophilus shows a particular specificity towards the formation of β-(1 → 6) glycosidic bonds. In order to develop more stable and economically cost-effective preparation, crude enzyme was successfully immobilized on a methacrylic polymer carrier Lifetech ECR8409, leading to its simultaneous 2-fold purification. In conclusion, this immobilized preparation showed unchanged specificity towards the transgalactosylation reaction, thus yielding 86 g/l GOS under the previously optimized conditions (lactose concentration 400 g/l in 0.1 M sodium phosphate buffer, pH 6.8 and temperature 50°C).

59 BASIC BIOLOGICAL SCIENCES↗

Uranium mobility across annual growth rings in three deciduous tree species

Black walnut (Juglans nigra), slippery elm (Ulmus rubra), and white ash (Fraxinus americana) trees were evaluated as potential archives of past uranium (U) contamination. Like other metals, U mobility in annual growth rings of trees is potentially dependent on the tree species. Uranium concentrations and isotopic compositions (masses 234, 235, 236, and 238) were analyzed by thermal ionization mass spectrometry to test the efficacy of using tree rings to retroactively monitor U pollution from the FFMPC, a U purification facility operating from 1951 to 1989. This study found non-natural U (depleted U and detectable 236U) in growth rings of all three tree species that pre-dated the start of operations at FFMPC and compositional trends that did not correspond with known contamination events. Therefore, the annual growth rings of these tree species cannot be used to reliably monitor the chronology of U contamination.

black walnut↗

Investigation of molybdate melts as an alternative method of reprocessing used nuclear fuel

Here, an investigation of molybdate melts containing sodium molybdate (Na 2 MoO 4 ) and molybdenum trioxide (MoO 3 ) to achieve the separation of uranium from fission products by crystallization has been performed. The separation is based on the difference in solubility of the fission product metal oxides compared to the uranium oxide or molybdate in the molybdate melt. The molybdate melt dissolves uranium dioxide at high temperatures, and upon cooling, uranium precipitates as uranium dioxide or molybdate, whereas the fission product metals remain soluble in the melt. Small-scale experiments using gram quantities of uranium dioxide have been performed to investigate the feasibility of UO 2 purification from the fission products. The composition of the uranium precipitate as well as data for partitioning of several fission product surrogates between the uranium precipitate and molybdate melt for various melt compositions are presented and discussed. The fission products Cs, Sr, Ru and Rh all displayed very large distribution ratios. The fission products Zr, Pd, and the lanthanides also displayed good distribution ratios (D > 10). A melt consisting of 20 wt% MoO 3 -50 wt% Na 2 MoO 4 -30 wt% UO 2 heated to 1313 K and cooled to 1123 K for the physical separation of the UO 2 product from the melt, and washed once with Na 2 MoO 4 displays optimum conditions for separation of the UO 2 from the fission products.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Gas-solid reaction pathway for chlorination of rare earth and actinide metals using hydrogen and chlorine gas

Hydriding and chlorination of buttons of metallic cerium have been tested as a head-end step to separating metal impurities from actinides. The objective here was to achieve complete conversion to chlorides while maintaining high surface area via small particles and open porosity. Hydriding by reaction with 100% H 2 gas at 573 K was successful at reducing cm-scale metal buttons into small particles/fragments. This step was followed by reaction with flowing 99.5% anhydrous Cl 2 gas at temperatures ranging from 423 to 573 K for 60 min. In experiments reported here, up to 92% conversion to cerium chloride was achieved from reacting with the anhydrous chlorine gas. The final chloride product has high porosity coupled with small particle sizes (microns to 1600 μm), which makes it suitable for subsequent purification processes. Higher chlorine concentrations in the gas favor higher conversion to chloride. The optimal temperature to achieve high chlorination is 523 K. Oxygen is a minor impurity in the chlorine gas which appears to prevent complete chlorination from being achieved.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗

A novel protocol to recycle zirconium from zirconium alloy cladding from used nuclear fuel rods

A potential new zirconium recycling protocol has been demonstrated using unirradiated Zircaloy-based claddings and depleted uranium oxide for the chemical removal of zirconium alloy cladding in used nuclear fuel (UNF) rods from light water reactors. This protocol is based on the application of three new scientific findings. First, a new lower temperature chlorination reaction of zirconium with sulfur monochloride is described. Second, the high solubility of zirconium chloride in thionyl chloride is used to separate it from uranium oxide fuel and fission and activation contaminants. Finally, in the third step, the zirconium chloride is purified by simple recrystallization from thionyl chloride. Utilizing sulfur chloride solvents for a lower temperature liquid-based chemical digestion and purification of zirconium alloy claddings reduces technical complications experienced by current high temperature gas phase chlorination strategies, such as contamination of product streams. This novel protocol has been demonstrated on a 3–50 g scale of unirradiated zirconium alloy, with no significant change in the time required for complete chlorination (3–4 h). This zirconium chlorination protocol has also been performed in the presence of depleted uranium oxide pellets. The depleted fuel pellets do not affect zirconium chlorination, and the chlorination protocol does not chemically or physically alter the fuel pellets. Finally, a preliminary description of an industrial protocol to recycle nuclear grade zirconium from UNF rods is presented.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Mitrocomin from the jellyfish Mitrocoma cellularia with deleted C-terminal tyrosine reveals a higher bioluminescence activity compared to wild type photoprotein

The full-length cDNA genes encoding five new isoforms of Ca2 +-regulated photoprotein mitrocomin from a small tissue sample of the outer bell margin containing photocytes of only one specimen of the luminous jellyfish Mitrocoma cellularia were cloned, sequenced, and characterized after their expression in Escherichia coli and subsequent purification. The analysis of cDNA nucleotide sequences encoding mitrocomin isoforms allowed suggestion that two isoforms might be the products of two allelic genes differing in one amino acid residue (64R/Q) whereas other isotypes appear as a result of transcriptional mutations. In addition, the crystal structure of mitrocomin was determined at 1.30 Å resolution which expectedly revealed a high similarity with the structures of other hydromedusan photoproteins. Although mitrocomin isoforms reveal a high degree of identity of amino acid sequences, they vary in specific bioluminescence activities. At that, all isotypes displayed the identical bioluminescence spectra (473–474 nm with no shoulder at 400 nm). Fluorescence spectra of Ca2 +-discharged mitrocomins were almost identical to their light emission spectra similar to the case of Ca2 +-discharged aequorin, but different from Ca2 +-discharged obelins and clytin which fluorescence is red-shifted by 25–30 nm from bioluminescence spectra. The main distinction of mitrocomin from other hydromedusan photoproteins is an additional Tyr at the C-terminus. Using site-directed mutagenesis, we showed that this Tyr is not important for bioluminescence because its deletion even increases specific activity and efficiency of apo-mitrocomin conversion into active photoprotein, in contrast to C-terminal Pro of other photoproteins. Since genes in a population generally exist as different isoforms, it makes us anticipate the cloning of even more isoforms of mitrocomin and other hydromedusan photoproteins with different bioluminescence properties.

59 BASIC BIOLOGICAL SCIENCES↗

Nano-phase formation accompanying phase separation in undercooled CoCrCuFeNi-3 at.% Sn high entropy alloy

Highlights: • Undercooled multi-component CoCrCuFeNi-3 at.% Sn high-entropy alloy was studied. • Accompanying phase separation, the nano-precipitates were detected. • The effect of Sn on the microstructures and properties was clarified. • The microhardness increased markedly with the increase of undercooling. - Abstract: Highly undercooled multi-component CoCrCuFeNi-3 at.% Sn high-entropy alloy was studied by adopting molten glass purification combined with cycle superheating methods. Based on the critical undercooling ΔT{sup ⁎}, the characteristic of liquid-phase separation was researched at different undercoolings. Accompanying phase separation, two phases (CoCrFeNi-rich and CuNi-rich) and three kinds of nano-precipitates (CrCo-rich, CrSn-rich and Sn-rich nano-precipitates) were detected. The microhardness of undercooled CoCrCuFeNi-3 at.% Sn high-entropy alloys increased markedly with the increase of undercooling. The effect of Sn on the microstructure evolution and properties in the process of phase separation was clarified with the aid of nano-precipitates.

36 MATERIALS SCIENCE↗

Fe{sub 3}O{sub 4} and CdS based bifunctional core–shell nanostructure

Highlights: ► First report on a room temperature aqueous process for growth of a hybrid core shell nanostructure containing a magnetic core and a semiconducting shell. ► Formation of distinct core shell nanostructure revealed by high resolution transmission electron microscopy. ► A bifunctional nature combining magnetic as well as photoresponce for the as synthesised core shell nanostructures demonstrated. ► A tendency towards self organisation of the core–shell nanostructure. ► Possible applications including purification and isolation of biological materials, drug delivery system, bio-labels, spintronics, etc. -- Abstract: A room temperature solution process for synthesis of Fe{sub 3}O{sub 4} nanoparticles and their hybrid core shell nanostructures using CdS as the shell material has been described. The as grown particles have been characterised using XRD, Rietveld refinement, high resolution transmission electron microscopy, atomic force microscopy, superconducting quantum interference device, optical absorbance and photoluminescence spectroscopy. A superparamagnetic response revealed from the magnetisation measurements of the as synthesised magnetite nanoparticles was retained even after the growth of the CdS shell. From luminescence and high resolution atomic force microscopy measurements, it is shown that the core–shell structures advantageously combine magnetic as well as fluorescence response with a tendency towards self-organization.

36 MATERIALS SCIENCE↗

Solvothermal in situ synthesis of Fe{sub 3}O{sub 4}-multi-walled carbon nanotubes with enhanced heterogeneous Fenton-like activity

Graphical abstract: After purification, the multi-wall carbon nanotubes (MWCNTs) act as seeds for Fe{sub 3}O{sub 4} nanoparticles heterogeneous nucleation. The Fe{sub 3}O{sub 4} nanoparticles with diameter range of 4.2–10.0 nm synthesized in situ on the MWCNTs under solvothermal condition. The formed nano Fe{sub 3}O{sub 4}-MWCNTs decolorized the Acid Orange II effectively via Fenton-like reaction. Highlights: ► The amount of water tunes size and size distribution of the Fe{sub 3}O{sub 4} nanoparticles (FNs). ► FNs are homogeneously coated on the multi-walled carbon nanotubes (MWCNTs). ► FNs have diameters in the range of 4.2–10.0 nm, average grain size of 7.4 nm. ► Fe{sub 3}O{sub 4}-MWCNTs are used as a Fenton-like catalyst to decompose Acid Orange II. ► Fe{sub 3}O{sub 4}-MWCNTs displayed a higher activity than nanometer-size Fe{sub 3}O{sub 4}. -- Abstract: Fe{sub 3}O{sub 4}-multi-walled carbon nanotubes (Fe{sub 3}O{sub 4}-MWCNTs) hybrid materials were synthesized by a solvothermal process using acid treated MWCNTs and iron acetylacetonate in a mixed solution of ethylene glycol and ultrapure water. The materials were characterized using X-ray powder diffraction, scanning and transmission electron microscopy, X-ray photoelectron spectroscopy, and vibrating sample magnetometry. The results showed that a small amount of water in the synthesis system played a role in controlling crystal phase formation, size of Fe{sub 3}O{sub 4}, and the homogeneous distribution of the Fe{sub 3}O{sub 4} nanoparticles deposited on the MWCNTs. The Fe{sub 3}O{sub 4} nanoparticles had diameters in the range of 4.2–10.0 nm. They displayed good superparamagnetism at room temperature and their magnetization was influenced by the reaction conditions. They were used as a Fenton-like catalyst to decompose Acid Orange II and displayed a higher activity than nanometer-size Fe{sub 3}O{sub 4}.

36 MATERIALS SCIENCE↗

Photoactive transparent nano-crystalline glass-ceramic for remazole red dye degradation

Graphical abstract: Display Omitted Highlights: ► Preparation and characterization of novel transparent nanocrystalline glass-ceramic. ► Precipitation of photoactive phases by using controlled heat-treatment. ► Conservation of transparency along with photoactivity. ► Using the prepared nanocrystalline glass-ceramic in water purification. -- Abstract: Transparent glass ceramic material was prepared from alkali-borosilicate glass containing titania by proper heat treatment scheme. The prepared samples were characterized using differential thermal analysis, X-ray diffraction, transmission electron microscope, selected area electron diffraction and UV–visible spectroscopy. The applied heat treatment program allowed the crystallization of nano-crystalline anatase, rutile, barium titanate, titanium borate and silicate phases while maintaining the transparency. The precipitated nano-crystalline anatase and rutile phases were responsible for the observed high photocatalytic activity of the prepared samples. Samples of 24.29 and 32.39 TiO{sub 2} wt% showed better efficiency for the decolorization of remazole red dye compared with commercial-TiO{sub 2} used in preparation of glass-ceramic. The reuse of prepared glass-ceramic photocatalyst with nearly same efficiency for different times was also proved.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Triazoloisoquinoline-based dual functional dyestuff for dye-sensitized solar cells

Graphical abstract: They consist of treating triazoloisoquinolines substituted tetramethyl-dioxaborolane (2) with 5-formyl-2-bromothiophene under conditions for Suzuki coupling to produce 5-(4-(3-oxo-[1,2,4]triazolo[3,4-a]isoquinolin-2(3H)-yl)phenyl) thiophene-2-carbaldehyde (3). Knoevenagel condensation of compound 3 with cyanoacrylic acid is carried out in the presence of piperidine, and after precipitation and purification with silica gel chromatography, the final dyestuff 4L is obtained as a yellow powder. This product has been characterized by spectroscopic analyses. Display Omitted Highlights: ► This new dyestuff investigated the role of triazoloisoquinoline dyestuffs as co-adsorbents and co-sensitizers with N719. ► The results show that co-adsorption of N719 sensitizer with dyestuff 5 increases the photocurrent in 1–0.25 molar ratio. ► This improved conversion efficiency is attributed to the insulating molecular layer, and the light harvesting effect at shorter-wavelength regions. -- Abstract: Triazoloisoquinoline contains electron-rich nitrogen and oxygen heteroatoms in a heterocyclic structure with high electron-donating ability. By utilizing this feature, two organic dyesutffs containing triazoloisoquinoline were synthesized and used in the fabrication of dye-sensitized solar cells (DSSCs), overcoming the deficiency of ruthenium dyestuff absorption in the blue part of the visible spectrum. This method also fills the blanks of ruthenium dyestuff sensitized TiO{sub 2} film, and forms a compact insulating molecular layer due to the nature of small molecular organic dyestuffs. The incident photon-to-electron conversion efficiency of N719 at shorter wavelength regions is 35%. After addition of triazoloisoquinoline-based dyestuff for co-sensitization, the IPCE at 350–500 nm increased significantly. This can be attributed to the increased photocurrent of the cells, which improves the dye-sensitized photoelectric conversion efficiency from 4.49% to 5.15%, which the overall conversion efficiency increased by about 15%. As a consequence, this low molecular weight organic dyestuff is a promising candidate as co-adsorbent and co-sensitizer for highly efficient dye-sensitized solar cells.

36 MATERIALS SCIENCE↗

Three-dimensional sea-urchin-like hierarchical TiO{sub 2} microspheres synthesized by a one-pot hydrothermal method and their enhanced photocatalytic activity

Graphical abstract: SEM images of the samples synthesized at different hydrothermal temperatures for 8 h: (a) 75; (b) 100; (c) 120; and (d) 140°C, followed by calcination at 450 °C for 2 h. Highlights: ► Effects of calcination temperature on the phase transformation were studied. ► Effects of hydrothermal temperature and time on the morphology growth were studied. ► A two-stage reaction mechanism for the formation was presented. ► The photocatalytic activity was evaluated under sunlight irradiation. ► Effects of calcination temperature on the photocatalytic activity were studied. - Abstract: Novel three-dimensional sea-urchin-like hierarchical TiO{sub 2} superstructures were synthesized on a Ti plate in a mixture of H{sub 2}O{sub 2} and NaOH aqueous solution by a facile one-pot hydrothermal method at a low temperature, followed by protonation and calcination. The results of series of electron microscopy characterizations suggested that the hierarchical TiO{sub 2} superstructures consisted of numerous one-dimensional nanostructures. The microspheres were approximately 2–4 μm in diameter, and the one-dimensional TiO{sub 2} nanostructures were up to 600–700 nm long. A two-stage reaction mechanism, i.e., initial growth and then assembly, was proposed for the formation of these architectures. The three-dimensional sea-urchin-like hierarchical TiO{sub 2} microstructures showed excellent photocatalytic activity for the degradation of Rhodamine B aqueous solution under sunlight irradiation, which was attributed to the special three-dimensional hierarchical superstructure, and increased number of surface active sites. This novel superstructure has promising use in practical aqueous purification.

36 MATERIALS SCIENCE↗

TiO{sub 2}/Bi{sub 2}(BDC){sub 3}/BiOCl nanoparticles decorated ultrathin nanosheets with excellent photocatalytic reaction activity and selectivity

Graphical abstract: TiO{sub 2}/Bi{sub 2}(BDC){sub 3}/BiOCl nanoparticles decorated ultrathin nanosheets showed excellent photocatalytic reaction activity and selectivity. - Highlights: • TiO{sub 2}/Bi{sub 2}(BDC){sub 3}/BiOCl nanoparticles decorated ultrathin nanosheets were synthesized through a facile hydrothermal process. • The products showed excellent photocatalytic activities for the degradation of various dyes. • The photocatalytic activities of the composite materials could be easily adjusted through tuning the content of TiO{sub 2}. • TiO{sub 2}/Bi{sub 2}(BDC){sub 3}/BiOCl displayed obvious photocatalytic selectivity in mixed dyes systems of rhodamine B and eosin Y. - Abstract: Photocatalysts with excellent photocatalytic reaction activity and ideal selectivity are highly desirable for pollutants clearance and purification of targeted organics from a mixture. Continued efforts toward the goal, we here present a facile hydrothermal route to synthesize TiO{sub 2}/Bi-benzenedicarboxylate/BiOCl nanoparticles decorated ultrathin nanosheets with a thickness less than 5 nm on a large scale. The as-synthesized products showed excellent photocatalytic activities for the degradation of various dyes such as rhodamine B, eosin Y and methylene blue in aqueous solution under visible light irradiation. The photocatalytic activities of TiO{sub 2}/Bi-benzenedicarboxylate/BiOCl nanocomposites for the degradation of rhodamine B and eosin Y could be adjusted through tuning the content of TiO{sub 2}. With increasing the amount of TiO{sub 2}, the composites showed declining photocatalytic activities in decomposing of rhodamine B while on the contrary they displayed enhanced photocatalytic activities in decomposing of eosin Y. Interestingly, TiO{sub 2}/Bi-benzenedicarboxylate/BiOCl composite nanosheets showed obvious photocatalytic selectivity in a mixed dyes system. The photocatalytic reaction and selectivity mechanisms of the nanocomposites for the degradation of the dyes were discussed on the basis of experimental results. The current study not only develops a new methodology to synthesize ultrathin nanosheets but also provides a novel strategy to design composite photocatalysts with high reaction activity and good selectivity.

36 MATERIALS SCIENCE↗

Fabrication of magnetic core PEI-silica shell particles

Highlights: • PEI-silica shell fabrication was developed for iron-carbonyl core material. • Magnetic separation of core-free by-product of the fabrication proved successful. • Varying fabrication method/concentration successfully tuned shell characteristics. • Sonication methods produced smooth coatings with a trend towards multicore particles. • Raspberry-like coatings were made by the slow addition, one- and two-pot methods. - Abstract: Magnetic core-silica shell particles combine the physico-chemical properties of the silica shell with the magnetic properties of the core. Seven possible particle coating methods utilizing the biomimetic polyamine polyethyleneimine (PEI) as the silication catalyst, have been identified and the objective of this study was to link the properties of the final PEI-silica coating with the methodology. The PEI-silica coated carbonyl iron particles were characterized via scanning electron microscopy, energy dispersive X-ray spectroscopy and Fourier transfer infrared spectroscopy. Varying the fabrication method and silane concentration successfully tuned the shell characteristics. Methods using sonication produced smooth more evenly distributed coatings with a tendency towards multicore particles. In contrast, raspberry-like coatings were produced via the slow addition, one- and two-pot methods. The magnetic separation process after synthesis achieved a degree of purification that makes these core–shell particles useful for potential applications that require specific surface interactions and the ease of magnetic separation.

36 MATERIALS SCIENCE↗

In-situ packaging ultra-uniform 3D hematite nanotubes by polyaniline and their improved gas sensing properties

Highlights: • Ultra-uniform 3D α-Fe{sub 2}O{sub 3} nanotubes were packaged by PANI through the two-stage solution processes. • PANI/α-Fe{sub 2}O{sub 3}-based sensor could detect low concentration of acetone (1 ppm) at lower temperature of 180 °C. • The unique structure of α-Fe{sub 2}O{sub 3} support and its synergetic effect with PANI layers improved the sensor performances. - Abstract: This paper reports the PANI (polyaniline)-packaged three-dimensional (3D) α-Fe{sub 2}O{sub 3} nanotubes P/N heterojunction, which was constructed successfully though a facile hydrothermal reaction without adding any surfactant followed by in-situ chemical polymerization in the liquid phase. The structure and morphology of the products were characterized by means of FESEM, XRD, TEM & HRTEM, TGA and FT-IR. Gas sensing test results found that, the PANI/α-Fe{sub 2}O{sub 3} nanocomposite sensor exhibited obviously higher response, lower working temperature (180 °C), fast response and recovery speeds, good selectivity and excellent stability to acetone gas, indicating its promising application for high-performance acetone sensors. The enhanced gas sensing performances can be attributed to the factors like ultra-uniform 3D nanotube-like structure for α-Fe{sub 2}O{sub 3}, the noticeable advantages of PANI, as well as the construction of heterojunction barrier at their interface. The as-prepared PANI/α-Fe{sub 2}O{sub 3} nanocomposite may be also applied in other areas like photocatalysis, water purification, ion batteries, optical devices, and so on.

77 NANOSCIENCE AND NANOTECHNOLOGY↗