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In continuation of our research work to develop new methodologies for organic transformations, [22 25] we observed that silica supported sodium hydrogen sulphate is a highly efficient catalyst for the synthesis of 1,1-diacetates (acylals) from the reaction of aldehydes with acetic anhydride under solvent-free conditions.
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We present a generic methodology for organic Rankine cycle optimization, where the working fluid is included as an optimization parameter, in order to maximize the net power output of the cycle.
The anticorrosive properties of undoped polyaniline (PAni) casted onto mild- and galvanised steels were studied by a classical methodology used for organic coatings.
Self-assembled nanostructures (SANs), therefore, play a major role in bioengineering stem cell niches, and in this chapter we explore three overarching methodologies for fabricating organic-based SANs.
The objective of this paper is to develop a thermo-economic design methodology for an Organic Rankine Cycle (ORC) based on the specific investment cost (SIC), taking into account changing operating conditions and part load behavior.
A series of new hybrid donor-acceptor materials based on hexabenzocoronenes (HBC) functionalized with electron donors is investigated by combining a variety of quantum mechanical and molecular dynamic methodologies for use in organic photovoltaic (OPV) devices.
The new methodology will be useful for organic synthetic chemists as well as others working in associated fields.
Reverse osmosis (RO) is one of the most promising and efficient methodologies for removing such harmful organic compounds from wastewater.
Different methodologies for the analysis of organic carbon, particularly the bioavailable fractions, as well as for the analysis of biomass on granulated materials are discussed and compared.
This work presents a preliminary design methodology and working fluid selection for organic Rankine cycle units featuring multistage axial turbines.
The increasing prevalence and success of organo-fluorines have instigated enormous efforts over the past decades in developing methodologies for efficiently introducing fluorine into organic molecules, however the unique properties of fluorine make these chemical incorporations challenging, usually needing harsh synthetic conditions and giving rise to moderate chemo- or stereo- selectivity.
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