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The proper acidity can be chosen to make the catalyst have good catalytic performance in the alkylation process.
The IC-modification that increases the SDO, QO, and IFCCO or decreases the SDFe can make the catalyst more powerful.
On the contrary, the thermal treatment at 600 °C results in the presence of nanoparticles larger than 4 nm that make the catalyst poorly active and selective.
The large number of surface Pt atoms and the synergetic effect of Pt, Ir and ReOx species make the catalyst efficiently generate hydrogen by aqueous phase reforming of sorbitol, and the generated hydrogen is consumed in the hydrogenolysis CO bonds.
In addition, CeO2 inhibit the sintering or phase transition of anatase TiO2 and make the catalyst keep the high surface area, which was favorable to keep more acid sites.
It was found instead that the use of ZrO2 Al2O3 as an alternative of the Al2O3 support was effective in lowering the dependence on Pt loading of the Pt BaO for the NSR catalysis since the ZrO2 Al2O3 support could make the catalyst highly selective for the formation of N2 under the rich condition, at a lower Pt loading.
Similar(53)
It should be noted that using impregnation method to make the catalysts, there is no any factor to control the particle size and metal particles disperse randomly in outer and inner surfaces of the CNTs.
By linking palladium to phenanthrolines modified with sulfur-containing groups, they made the catalyst water soluble.
The addition of Pd makes the catalyst more selective towards acetic acid formation.
This process might also wash away the impregnated MgO making the catalyst lose even more its transesterification activity.
The unique nanostructure makes the catalyst to be a novel and welcoming choice for H2O2 favorite reactions.
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