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Blends of high strength PNEA50PhPh50 and 85:15 PLAGA are promising biomaterials for a variety of musculoskeletal applications.
It is assumed that the blends of high and low molecular weight PIB could affect these properties.
In this study, blends of high strength poly[ 50% ethyl alanato) (50% p-phenyl phenoxy) phosphazene] (PNEA50PhPh50) and 85:15 PLAGA were prepared using a mutual solvent approach.
These findings reveal that the surface of blends of high molecular weight polymers may not be in the thermodynamic equilibrium state.
In this paper we prepare co-continuous blends of high density polyethylene/polystyrene in order to compare various microstructural characterization techniques.
In this work, we investigated the epitaxial crystallization and its determinant factor in the blends of high density polyethylene (HDPE) and a low crystallizable propylene-ethylene random copolymer (PPR) during injection molding.
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Blends of high-density polyethylene (HDPE) and PPDL were shown to be immiscible at the onset of crystallization of polyethylene, resulting in phase-separated morphologies.
Furthermore, ternary blends of high-oleic sunflower oil, castor oil (CO) and EVA may be used to design enhanced bio-lubricant formulations for some specific applications.
We investigate the gradual changes of the microstructure of two blends of high-density polyethylene (HDPE) and polyamide 6 (Pat) at opposite composition filled with increasing amounts of an organomodified clay.
The phase behaviour of blends of high-molecular weight poly N-vinyl poly N-vinyl (pyrrolidonehort-chain PVPy(ethylene glycol) (PEG) of Mwith0, prepared by drying their solutions in a common solvent (ethyl alcohol), was studied using DSC.
As a part of long-term project aimed at super polyolefin blends, in this work, we report the mechanical reinforcement and phase morphology of the blends of high-density polyethylene (HDPE) and ethylene vinyl acetate (EVA) achieved by dynamic packing injection molding.
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