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On-line measurement of biomass coal blends is very important for developing appropriate subsidy policies for biomass co-firing power generation.
The crystalline morphology of the blends is very complex and depends strongly on the thermal history in the melt, the crystallization temperature and blend composition.
Further, the behaviour of these blends is very similar to that which has been found for binary linear/lightly branched polyethylene blend systems where the copolymers were polymerized by other processes.
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Typical industrial techniques, like rolling ball blends, are very labor intensive.
Weldline strength of the blends was very poor compared to PC, but improved with increasing rubber content in SAN.
This suggests that local free volume properties of polymer in blends are very important for local packing and segmental arrangements.
The thermal properties of m-LLDPE/m-HDPE blends are very similar to a single-component system.
Our results showed that the crystallization and morphology of compatible PTHF-b-PMMA/PTHF blends are very different from those of incompatible blends.
DMTA indicates that the Tg of the cured PVC/DAOP blends are very close to that of PVC and have a higher storage modulus at the rubbery region.
Activation spectra show that BPA polycarbonate (PC) and its blends are very sensitive to UV with wavelengths <300 nm, as is well-known in the literature, but other resins gave unremarkable results.
The morphologies of large-size PA6 particles encapsulated by SEBS or tiny PA6 particles and some larger-size SEBS agglomerates dispersed separately in PP matrix for the enhancement in mechanical properties of the blends are very limited.
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CEO of Professional Science Editing for Scientists @ prosciediting.com