CO2 capture using silica-immobilized dicationic ionic liquids with magnetic and non-magnetic properties.

The need to find alternative materials to replace aqueous amine solutions for the capture of CO2 in post-combustion technologies is pressing. This study assesses the CO2 sorption capacity and CO2/N2 selectivity of three dicationic ionic liquids with distinct anions immobilized in commercial mesoporous silica support (SBA- 15). The samples were characterized by UART-FTIR, NMR, Raman, FESEM, TEM, TGA, Magnetometry (VSM), BET and BJH. The highest CO2 sorption capacity and CO2/N2 selectivity were obtained for sample SBA@DIL_2FeCl4 [at 1 bar and 25 °C; 57.31 (±0.02) mg CO2/g; 12.27 (±0.72) mg CO2/g]. The results were compared to pristine SBA-15 and revealed a similar sorption capacity, indicating that the IL has no impact on the CO2 sorption capacity of silica. On the other hand, selectivity was improved by approximately 3.8 times, demonstrating the affinity of the ionic liquid for the CO2 molecule. The material underwent multiple sorption/desorption cycles and proved to be stable and a promising option for use in industrial CO2 capture processes.

Magnetically Stimulable Graphene Oxide/Polypropylene Nanocomposites.

Core-shell magnetic air-stable nanoparticles have attracted increasing interest in recent years. Attaining a satisfactory distribution of magnetic nanoparticles (MNPs) in polymeric matrices is difficult due to magnetically induced aggregation, and supporting the MNPs on a nonmagnetic core-shell is a well-established strategy. In order to obtain magnetically active polypropylene (PP) nanocomposites by melt mixing, the thermal reduction of graphene oxides (TrGO) at two different temperatures (600 and 1000 °C) was carried out, and, subsequently, metallic nanoparticles (Co or Ni) were dispersed on them. The XRD patterns of the nanoparticles show the characteristic peaks of the graphene, Co, and Ni nanoparticles, where the estimated sizes of Ni and Co were 3.59 and 4.25 nm, respectively. The Raman spectroscopy presents typical D and G bands of graphene materials as well as the corresponding peaks of Ni and Co nanoparticles. Elemental and surface area studies show that the carbon content and surface area increase with thermal reduction, as expected, following a reduction in the surface area by the support of MNPs. Atomic absorption spectroscopy demonstrates about 9-12 wt % metallic nanoparticles supported on the TrGO surface, showing that the reduction of GO at two different temperatures has no significant effect on the support of metallic nanoparticles. Fourier transform infrared (FT-IR) spectroscopy shows that the addition of a filler does not alter the chemical structure of the polymer. Scanning electron microscopy of the fracture interface of the samples demonstrates consistent dispersion of the filler in the polymer. The TGA analysis shows that, with the incorporation of the filler, the initial (Tonset) and maximum (Tmax) degradation temperatures of the PP nanocomposites increase up to 34 and 19 °C, respectively. The DSC results present an improvement in the crystallization temperature and percent crystallinity. The filler addition slightly enhances the elastic modulus of the nanocomposites. The results of the water contact angle confirm that the prepared nanocomposites are hydrophilic. Importantly, the diamagnetic matrix is transformed into a ferromagnetic one with the addition of the magnetic filler.

Polymorphism of the Co-Te nanophases in mechanochemical synthesis.

The mechanochemical synthesis of all cobalt tellurides' phases is demonstrated in this work. The samples had their structural, microstructural, and magnetic characterizations performed by X-ray powder diffraction, transmission electron microscopy, and magnetometry techniques. The initial atomic stoichiometries tested of Co32Te68 and Co40Te60 resulted in the synthesis of the γ-CoTe2 Pnnm (marcasite), α-CoTe2 Pa3̄ (pyrite), α-CoTe2 P3̄m1 (CdI2-like), and ß-CoTe P63/mmc phases with different weight proportions in the sample. Modeling of the X-ray diffractograms employed conventional double-Voigt and crystallite shape-anisotropy DV approaches to show that the volumetric diameter average and true crystallite size of the diffraction domains are in the range of tens of nanometers. Transmission electron microscopy measurements also allowed distribution counting of the crystallite sizes via maximum caliper diameter. Electron diffraction experiments presented comparable structural parameters with Rietveld via the analysis of the Debye rings. A model using the Langevin approaches showed the phases to present both ferromagnetic and superparamagnetic contributions attributed to weakly-interacting metallic Co grains with magnetic domain sizes ranging between 2.3 and 4.0 nm. The phases' evolution with storage time was analyzed over two years and revealed to be stable regarding their structural and microstructural properties.

Study of the Influence of Magnetite Nanoparticles Supported on Thermally Reduced Graphene Oxide as Filler on the Mechanical and Magnetic Properties of Polypropylene and Polylactic Acid Nanocomposites.

A study addressed to develop new recyclable and/or biodegradable magnetic polymeric materials is reported. The selected matrices were polypropylene (PP) and poly (lactic acid) (PLA). As known, PP corresponds to a non-polar homo-chain polymer and a commodity, while PLA is a biodegradable polar hetero-chain polymer. To obtain the magnetic nanocomposites, magnetite supported on thermally reduced graphene oxide (TrGO:Fe3O4 nanomaterial) to these polymer matrices was added. The TrGO:Fe3O4 nanomaterials were obtained by a co-precipitation method using two types of TrGO obtained by the reduction at 600 °C and 1000 °C of graphite oxide. Two ratios of 2.5:1 and 9.6:1 of the magnetite precursor (FeCl3) and TrGO were used to produce these nanomaterials. Consequently, four types of nanomaterials were obtained and characterized. Nanocomposites were obtained using these nanomaterials as filler by melt mixer method in polypropylene (PP) or polylactic acid (PLA) matrix, the filler contents were 3, 5, and 7 wt.%. Results showed that TrGO600-based nanomaterials presented higher coercivity (Hc = 8.5 Oe) at 9.6:1 ratio than TrGO1000-based nanomaterials (Hc = 4.2 Oe). PLA and PP nanocomposites containing 7 wt.% of filler presented coercivity of 3.7 and 5.3 Oe, respectively. Theoretical models were used to analyze some relevant experimental results of the nanocomposites such as mechanical and magnetic properties.

Polysulfone metal-activated carbon magnetic nanocomposites with enhanced CO2 capture.

In the present study, polysulfone (PSF)-activated carbon nanocomposites were synthesized by a melt mixing technique. Here, 2 wt% activated carbon (CA, CA-Ni, and CA-Co) was used as filler, and effects on thermal, mechanical, magnetic, morphological, and carbon dioxide capture properties were studied. The pyrolysis of wood sawdust produced carbon materials activated by Co and/or Ni salt. The thermal degradation and the amount of metal in the carbon materials were investigated by thermogravimetric analysis. The maximum degradation temperature showed an improvement of up to 3 °C, while the initial degradation temperature decreased up to 4 °C with the addition of metal-activated carbons. The values of T g estimated by differential scanning calorimetry appear to be practically identical for pure PSF and its nanocomposites. The elasticity modulus of the nanocomposite shows an enhancement of 17% concerning the neat PSF. The water contact angle showed a decrease with the incorporation of the fillers, indicating the hydrophilic nature of the composite. The carbon dioxide sorption capacity of the nanocomposite showed an enhancement of almost 10% in contrast to neat PSF. Ferromagnetic behavior of the thermoplastic nanocomposite was observed with the introduction of 2.0 wt% metal-carbonized filler. The exceptional magnetic properties, for a thermoplastic material such as polysulfone, make it promising for various industrial applications.

Tunable High-Field Magnetization in Strongly Exchange-Coupled Freestanding Co/CoO Core/Shell Coaxial Nanowires.

The exchange bias properties of Co/CoO coaxial core/shell nanowires were investigated with cooling and applied fields perpendicular to the wire axis. This configuration leads to unexpected exchange-bias effects. First, the magnetization value at high fields is found to depend on the field-cooling conditions. This effect arises from the competition between the magnetic anisotropy and the Zeeman energies for cooling fields perpendicular to the wire axis. This allows imprinting predefined magnetization states to the antiferromagnetic (AFM) shell, as corroborated by micromagnetic simulations. Second, the system exhibits a high-field magnetic irreversibility, leading to open hysteresis loops attributed to the AFM easy axis reorientation during the reversal (effect similar to athermal training). A distinct way to manipulate the high-field magnetization in exchange-biased systems, beyond the archetypical effects, was thus experimentally and theoretically demonstrated.

Magnetoelectric effect and phase transitions in CuO in external magnetic fields.

Apart from being so far the only known binary multiferroic compound, CuO has a much higher transition temperature into the multiferroic state, 230 K, than any other known material in which the electric polarization is induced by spontaneous magnetic order, typically lower than 100 K. Although the magnetically induced ferroelectricity of CuO is firmly established, no magnetoelectric effect has been observed so far as direct crosstalk between bulk magnetization and electric polarization counterparts. Here we demonstrate that high magnetic fields of ≈ 50 T are able to suppress the helical modulation of the spins in the multiferroic phase and dramatically affect the electric polarization. Furthermore, just below the spontaneous transition from commensurate (paraelectric) to incommensurate (ferroelectric) structures at 213 K, even modest magnetic fields induce a transition into the incommensurate structure and then suppress it at higher field. Thus, remarkable hidden magnetoelectric features are uncovered, establishing CuO as prototype multiferroic with abundance of competitive magnetic interactions.