28 research outputs found

    Catalysts based on Co-Birnessite and Co-Todorokite for the efficient production of hydrogen by ethanol steam reforming

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    [EN] Two structured manganese oxides (Birnessite and Todorokite) containing Co have been studied in the steam reforming of ethanol. It has been found that both materials are active in the hydrogen production, exhibiting high values of conversion of ethanol and selectivities to hydrogen (100% and 70%, respectively). The best results have been obtained with the catalyst based on Todorokite material. Characterization by DRX, BET area, TPR and TEM has allowed to find that the excellent performance exhibited by this material could be attributed to the lower size of the Co metallic particles present in this sample (6 nm vs 12 nm in Birnessite). This lower size could be related to the especial microporous structure of Todorokite precursor, which could provide high-quality positions for the stabilization of the Co metal particles during calcination and reduction steps. Catalytic deactivation has also been considered. Deactivation was found higher for Todorokite-based catalyst, which presented the largest amount of deposited carbon (26.2 wt% for Co-TOD vs 10.6 wt% for Co-BIR). On the other hand, the degree of metal sintering was found similar in both catalysts. Therefore, the deactivation of the catalysts has been attributed primarily to the deposition of coke. The results presented here show that it is possible to prepare new catalysts based on manganese oxides with Birnessite and Todorokite structure and promoted with Co with high catalytic performance in the steam reforming of ethanol. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.The doctor Javier Francisco Da Costa Serra acknowledges the CSIC for granted the scholarship predoctoral-JAE-CSIC. Moreover, Electronic Microscopy Service of UPV for TEM images.Da Costa Serra, JF.; Chica, A. (2018). Catalysts based on Co-Birnessite and Co-Todorokite for the efficient production of hydrogen by ethanol steam reforming. International Journal of Hydrogen Energy. 43(35):16859-16865. https://doi.org/10.1016/j.ijhydene.2017.12.114S1685916865433

    Metallurgical Evaluation and Condition Assessment of FSX 414 Nozzle Segments in Gas Turbines by Metallographic Methods

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    Gas turbine components such as nozzle segments, buckets, transition pieces, and combustio

    Cu promoted Ni-Co/hydrotalcite catalyst for improved hydrogen production in comparison with several modified Ni-based catalysts via steam reforming of ethanol

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    Enhanced hydrogen production via catalytic steam reforming of ethanol has a huge potential. In the present investigation, several combinations of mixed metal oxide supported catalysts were evaluated for efficient and economical hydrogen generation from ethanol. The comparison was carried out in terms of ethanol conversion, hydrogen yield and cyclic stability over various catalyst-support systems. Several nickel based supported catalysts namely, Ni/MgO, Ni/Al2O3, Ni/CeO2 and Ni/ZrO2 were studied in this work among which Ni/MgO and Ni/Al2O3 showed satisfactory activity and stability for hydrogen production. Thereafter Ni/hydrotalcite (HTc)-type material was employed to combine features of the above catalysts which showed more than 90% ethanol conversion and yielded 82 mol% of hydrogen at optimized conditions. Finally, a novel combination of Cu promoted Ni-Co/HTc was synthesized and tested for improved hydrogen production. It showed almost complete conversion of ethanol (98.3%) with hydrogen yield of 83% at much lower temperature (673 K). The process conditions were optimized by studying effects of temperature, S/C ratio and GHSV on hydrogen production. Cu-Ni-Co/HTc also remained stable for up to 4 cycles justifying its multi-cycle activity, selectivity and durability. Such novel combination of catalyst-support system assists in improved hydrogen production in a sustainable manner

    Mimosine functionalized gold nanoparticles (Mimo-AuNPs) suppress β-amyloid aggregation and neuronal toxicity

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    Evidence suggests that increased level/aggregation of beta-amyloid (Aβ) peptides initiate neurodegeneration and subsequent development of Alzheimer's disease (AD). At present, there is no effective treatment for AD. In this study, we reported the effects of gold nanoparticles surface-functionalized with a plant-based amino acid mimosine (Mimo-AuNPs), which is found to cross the blood-brain barrier, on the Aβ fibrillization process and toxicity. Thioflavin T kinetic assays, fluorescence imaging and electron microscopy data showed that Mimo-AuNPs were able to suppress the spontaneous and seed-induced Aβ1-42 aggregation. Spectroscopic studies, molecular docking and biochemical analyses further revealed that Mimo-AuNPs stabilize Aβ1-42 to remain in its monomeric state by interacting with the hydrophobic domain of Aβ1-42 (i.e., Lys16 to Ala21) there by preventing a conformational shift towards the β-sheet structure. Additionally, Mimo-AuNPs were found to trigger the disassembly of matured Aβ1-42 fibers and increased neuronal viability by reducing phosphorylation of tau protein and the production of oxyradicals. Collectively, these results reveal that the surface-functionalization of gold nanoparticles with mimosine can attenuate Aβ fibrillization and neuronal toxicity. Thus, we propose Mimo-AuNPs may be used as a potential treatment strategy towards AD-related pathologies

    Fluoride-free Hiyama coupling by palladium abnormal N-heterocyclic carbene complexes

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    A series of palladium complexes of the abnormal N-heterocyclic carbene ligands of the type (a-NHC)-PdI2(L) [L = NC5H5 (1-3)b and PPh3 (1-3)c] effectively catalyzed the Hiyama coupling of aryl bromides and iodides with PhSi(OMe)(3) under the highly desired fluoride-free conditions. Interestingly enough, the pyridine based trans-(1-3)b complexes and a PPh3 derived cis-3c complex exhibited higher yields than the related PPh3 derived trans-(1-2)c complexes. The superior performances of the pyridine based trans-(1-3)b complexes and the PPh3 derived cis-3c complex have been correlated to a tighter binding of the a-NHC ligand to the palladium center in these complexes, leading to a greater (a-NHC) ligand influence on the metal center partaking in the catalysis
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