Search results for "Inorganic chemist"
showing 10 items of 7340 documents
Molybdenum blue: Binding to collagen fibres and microcrystal formation
2005
Collagen fibres have been shown by transmission electron microscopy to progressively bind the polyoxomolybdate ring-complex, termed molybdenum blue. Nucleation of cuboidal molybdenum blue microcrystals occurs on the surface of the collagen fibres, leading eventually to extensive coating of the fibres with microcrystals.
Hydrodesulfurization cobalt-based catalysts modified by gold
2007
Cobalt catalysts supported on amorphous SiO2 and ordered mesoporous silica (MCM-41) were prepared by incipient wetness impregnation. Gold was added by consecutive impregnation or by co-impregnation. The materials were characterised by XPS, XRD and TPR techniques and evaluated in the hydrodesulfurization (HDS) of thiophene in order to investigate the effect of the noble metal on the structure and on the catalytic behaviour of the supported cobalt. Co/MCM-41 exhibited higher HDS activity and higher stability than the Co/SiO2. Moreover, in contrast to silica case, the gold impregnated MCM-41, produced an enhancement of the cobalt catalytic activity, and this is likely to be related to an incre…
Total oxidation of propane using nanocrystalline cobalt oxide and supported cobalt oxide catalysts
2008
Abstract Supported and unsupported nanocrystalline cobalt oxides have been shown to be extremely efficient catalysts for the total oxidation of propane. Total conversion with a high stability has been achieved at reaction temperatures as low as 250 °C. In the present work, a comparison between the catalytic performance of bulk and alumina-supported nanocrystalline cobalt oxide catalysts has been made. The influence of crystallite size, nature of the support (alpha, gamma and mesoporous alumina) and cobalt loading, has been probed. Unsupported cobalt oxide catalysts were more active than any supported cobalt oxide catalysts. The catalytic activity was mainly dependent on the crystallite size…
Optimized bath for electroless deposition of palladium on amorphous alumina membranes
2006
A new bath for the electroless deposition of palladium on anodic alumina (AA) membranes is proposed. It was found that the optimal conditions for the uniform deposition of palladium, with minimal damage to the AA membranes, were under conditions of pH 8.4 and plating times shorter than 30 min. The deposited Pd layer was detected by X-ray diffraction (XRD) and energy dispersive X-ray (EDX) analysis. The morphology of the AA membrane before and after plating was examined by scanning electron microscopy (SEM). EDX analysis revealed that palladium was deposited only on the surfaces of the membrane and Sn ions, coming from the sensitizing bath, were incorporated into the palladium layer. EDTA in…
Calcium silicate hydrates: Solid and liquid phase composition
2015
© 2015 Elsevier Ltd. This paper presents a review on the relationship between the composition the structure and the solution in which calcium silicate hydrate (C S H) is equilibrated. The silica chain length in C S H increases with the silicon concentration and the calcium content in the interlayer space with the calcium concentrations. Sodium and potassium are taken up in the interlayer space preferentially at low calcium concentrations and thus by low Ca/Si C S H. Aluminium uptake in C S H increases strongly at higher aluminium concentrations in the solution. At low Ca/Si aluminium substitutes silica in the bridging position at Ca/Si. > 1 aluminium is bound in TAH. Recently developed ther…
Preparation of polyelectrolyte-modified membranes for heavy metal ions removal
2017
ABSTRACTPolyethersulfone membranes were modified by polyelectrolyte (PE) multilayers, made of poly(allylamine hydrochloride) with poly(styrene sulfonate), to remove Cu2+, Zn2+ and Ni2+ heavy metal cations from aqueous solutions in a wide range of metal concentration (50–1200 ppm). After characterization of the modified membranes, the efficiency of the process was estimated for single heavy metal ions solution leading to high rejection rates (>90% for 50 ppm) and good adsorption capacities (7.0–8.5 mg cm−2) whatever the metal ion tested. The stability in time of the modified membranes was proved by repeating successive filtrations with the same membrane. The filtration process was also used …
From Mono- to Poly-Substituted Frameworks: A Way of Tuning the Acidic Character of C-c-H in o-Carborane Derivatives
2009
[EN] The incorporation of iodine atoms onto the boron vertices of the o-carborane framework causes, according to spectroscopic data, a uniform increase in the acidic character of the C-c-H (C-c= cluster carbon) vertices, whereas the incorporation of methyl groups onto the boron vertices of the o-carborane framework reduces their acidity. Methyl groups when attached to boron are electron-withdrawing in boron clusters, whereas iodine atoms bonded to boron act as electron donors. This has been proven on B-methyl and B-iodinated o-carboranes with NMR spectroscopy measurements and DFT calculations of natural bond orbital (NBO) charges. which show a Cumulative buildup of positive cluster only tot…
Formation and characterization of oxidic and metallic Fe/Ni multilayers prepared from Langmuir-Blodgett films
1994
Oxidic and metallic iron, nickel, and mixed iron/nickel mono- and multilayers were prepared by some treatments of iron- and nickel-containing Langmuir-Blodgett films. The layers were characterized by several surface-sensitive methods. Interactions between the iron and the nickel could be observed. The results are different to those obtained from disordered bulk alloys and from simple diffusion calculations.
Mössbauer and TEM studies of the perovskite system (1-y)La2/3 $$A$$ 1/3TiO3·yLaFeO3
1994
The microscopic nature of the Mossbauer phase analysis has been found as being particularly valuable in testing assumptions suggested by TEM results regarding the microdomain structure and the population of different lattice sites by iron ions in the perovskite system (1-y)La2/3\(A\)1/3TiO3·yLaFeO3 with 0.04<y < 0.25 (\(A\) is an A-site vacancy). This system was found to contain only Fe3+-phases which are stable under normal conditions, but moderate heating in vacuo causes a partial reduction of ferric ions to ferrous ions.
Crystal structure of the molecular adduct of dimethyltin(IV) chloride with N,N′-ethylenebis(salicylideneiminato) nickel(II)
1974
Abstract N,N′-Ethylenebis(salicylideneiminato)nickel(II) behaves as a neutral bidentate ligand through its oxygen atoms forming binuclear complexes with organotin(IV) chlorides. The crystal structure of the dimethyl derivative is reported.