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Consideration of Taylor et al.'s (2010 ▸) data for C-A-S-H that is present in 20-year-old water-activated blast-furnace slag/Portland cement blends indicates that f = in every T∞ module in all of the model structures and so it would seem plausible that the tetrahedral bridging sites are occupied alternately by Al and Si atoms.
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MDSC detected only one Tg for the SPS/SVP blends, indicating that the blends were unclustered.
Large deformation behavior of aged blends indicated that SEBS-g-MA performed best by far.
Blends of PA66 with syndiotactic PS compatibilized with PS-An gave very similar morphology to the PA66/PS blends indicating that these conclusions apply also to PA66/sPS blends.
Visual inspection of the SEM images of the blends indicated that the guest particles adhered to the surface of paracetamol resulting in effective formation of interactive mixtures.
The modulus of rupture and flexural modulus for all the cement-stabilized RCA/FRG blends indicate that these blends are suitable for applications such as cement-stabilized pavement bases/subbases.
It is also consistent with recent studies of melt and solid-state processing of blends indicating that in situ interpolymer radical coupling is useful in reactive compatibilization.
The effect of MAP on the mechanical properties of PP/LCP blends indicated that MAP interacted with the amide group preferentially over the ester group.
The morphology of the blends indicated that the EPDM phase was preferentially dispersed as domains in the continuous Sorona® matrix up to 30% of its concentration.
However, all methods show only a single glass transition in PPO/PS blends, indicating that the existence of two effective Tgs due to self-concentration effects is not a universal phenomenon in miscible polymer blends with a large Tg contrast.
Fourier transform infra-red spectra of these two blends indicate that the presence of the chlorine atom strengthens the attraction between the phenyl rings of P2CS and the electron lone pairs of the oxygen atoms on the PVME chains.
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