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Exact(10)
HAuCl4, as the metal precursor, was preferentially dissolved and coordinated into the corona of the micelles.
The metal precursor was present as Au III) (AuCl4−), or Au(I) (AuCl2−) in W or DCE.
Upon isolation at room temperature, the amide-imide mixed metal precursor was pyrolyzed at elevated temperatures under an ammonia flow by two different routes.
In the first method the metal precursor was introduced into the initial solution while in the impregnated samples the metal was spread over the carrier surface.
One-pot synthesis via confined mesopore using a citrate-based metal precursor was applied to obtain a perovskite-type metal oxide with a high surface area for total oxidation of toluene.
The metal precursor was heated to 150°C.
Similar(50)
For a metal precursor with a high concentration and a low melting point, the metal precursor is dissolved or molten in the liquid phase during drying.
The results described here show that the porosity and surface chemistry of the carbon support have a clear effect on iron loading, iron dispersion, catalytic activity (CO hydrogenation) and olefins selectivity when the metal precursor is iron nitrate and little effect if it is iron pentacarbonyl.
In these studies, the reaction mechanisms between green rust and soluble metal precursor were not detailed and none of the studies gave an evidence of metallic particles by X-ray diffraction (XRD).
The metal precursor is present in an aqueous phase, the reductant is present in an organic phase, and potential developed at the interface leads to spontaneous formation of metal nanoparticles which block the tip of the pipet, forming a disk-shaped nanoelectrode.
A variety of metal precursors was used to yield iron, platinum, and palladium decorated graphene sheets.
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