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DSC showed only one peak (86.9°C) for the blend sample, and FT-IR exhibited additional peaks (1545, 1625 cm−1) by the blending.
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A matrix-dispersed droplet morphology was noted for all blend samples, and the rubber particle size decreased with decreasing ACN content of NBR.
Miscibility was proved by the single composition dependent glass transition temperature over the entire composition range observed in DSC traces of the quenched blend samples and also by the melting point depression.
SEM analyses of the water-etched PLLA/PEO blend samples and ToF-SIMS analyses of the blend thin films indicated that the PEO content and thickness of the interspherulitic boundary region was higher in the (50/50) blend than in the (80/20) blend.
The level of attachment to pure sericin (sample 5) is higher than that to fibroin (sample 1) or a fibroin-rich blend (sample 2), and even to 50/50 blends (samples 3 and 3(G)).
DSC analysis of every blend sample showed a large and broad endothermic peak around 150 °C.
The cylinder diameter in this blend sample was 13.7 nm and the hexagonal lattice was a=23.1 nm.
Tensile test results for all the blend samples, with and without plasma-treated LDPE, are compared.
Each plasmid DNA blend sample was tested with one test kit lot, and a total of 24 replicates were tested per sample.
In terms of contact angle values, both BMSF and BMSS are expected to promote cell attachment, but the differences between BMSS (sample 5) and the blend samples 2, 3, and 3(G) (Table 1) are too small to justify the differences in cell attachment shown in Figure 5.
The blend sample of polymers was prepared by well established solution blending technique and their nanocomposite samples were prepared through dispersion technique during the solution casting of blend sample.
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