نتایج جستجو برای: cobalt based catalyst
تعداد نتایج: 2994791 فیلتر نتایج به سال:
Cobalt-containing polyoxotitanates (TiCo) are excellent precursors for the simple and scalable preparation of Nocera-type CoOx water-oxidation electrocatalysts. The TiCo cages serve as a reservoir for cobalt ions in a titania matrix on fluoride-doped tin oxide electrodes, and form, in situ, the active CoOx catalyst for O2 evolution with high stability in phosphate buffer in pH neutral water.
A new cobalt-catalysed reductive coupling of aryl halides with benzyl chlorides is reported; a variety of diarylmethanes can be prepared in good to excellent yields under mild reaction conditions using CoBr(2) as catalyst and Zn dust; this new cobalt-catalysed coupling represents a practical and interesting alternative to previously known methods for the synthesis diarylmethanes.
Nitrogen doped graphitic layer encased cobalt (N-C@Co) nanoparticles, as novel non-precious-metal catalysts for the oxygen reduction reaction (ORR), were fabricated by a facile method using cyanamide and cobalt nitrate as precursors. The N-C@Co catalysts exhibited comparable catalytic performance, better stability and improved methanol tolerance towards the ORR than those of the commercial Pt/C...
Cobalt pi-complexes, previously described in the literature and specially synthesized and characterized in this work, were used as catalysts in homogeneous oxidation of organic compounds with peroxides. These complexes contain pi-butadienyl and pi-cyclopentadienyl ligands: [(tetramethylcyclobutadiene)(benzene)cobalt] hexafluorophosphate, [(C₄Me₄)Co(C₆H₆)]PF₆ (1); diiodo(carbonyl)(pentamethylcyc...
Development of efficient, robust and earth-abundant water oxidation catalysts (WOCs) is extremely desirable for water splitting by electrolysis or photocatalysis. Herein, we report cobalt oxide nanoparticles anchored on the surface of sulfonated graphite (denoted as “CoOx@G-Ph-SN”) to exhibit unexpectedly efficient water oxidation activity with a turnover frequency (TOF) of 1.2 s ; two or three...
The role of lanthanides as promoters on cobalt-based catalysts for Fischer-Tropsch synthesis was evaluated under relevant biomass-derived syngas mixtures. Cerium, lanthanum and a combination them were impregnated an industrial micro-catalyst. Lanthanide incorporation did not affect significantly the morphology catalyst, although it reduced available surface cobalt. Catalytic tests revealed that...
A hybrid system with a coordinative interaction between a cobalt complex of a N2S2-tetradentate ligand and CdTe quantum dots displayed a high activity (initial TOF 850 h(-1)) and improved stability (TON 1.44 × 10(4) based on catalyst over 30 h) for the photochemical H2 generation from water, with a quantum efficiency of 5.32% at 400 nm.
In this study, two cobalt based catalyst samples were prepared on titania and titania nanotubes supports using the deposition precipitation method. Their structural configurations were characterized and compared using BET, and TRP analyses. The BET analysis showed that the surface area of TiO2 is much higher than that of TNT which was due to their structural differences. Analyses of the results...
بررسی کارایی CoFe2O4 با پایه گرافن در فعال سازی پراکسی مونوسولفات و حذف آموکسی سیلین از محیط های آبی
Background and purpose: Nowadays, amoxicillin is one of the most important and most frequently used antibiotics that has received especial attention as it causes resistance in bacteria. This compound enters the aquatic environment through different routes including sewage and waste disposal of medical centers, veterinary centers and industries. The aim of this study was to evaluate the performa...
in a novel dual bed reactor fischer-tropsch synthesis was studied by using two diffrent cobalt catalysts. an alkali-promoted cobalt catalyst was used in the first bed of a fixed-bed reactor followed by a rutenuim promoted cobalt catalyst in the second bed. the activity, product selectivity and accelerated deactivation of the system were assessed and compared with a conventional single bed react...
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