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Crystallinity of the polymer and drug changed, and was dependent upon curing temperature and time.
The CF3 unit decreases the crystallinity of the polymer, with 50% and 100% copolymers being amorphous.
The crystallinity of the polymer, the kinetics of crystallization, and the influence of surface functionalization on thermal conductivity were also investigated.
Differential scanning calorimetry showed a decrease in the crystallization temperature and crystallinity of the polymer with the addition of both wrapped and non-wrapped SWCNTs.
Additionally, the effect of heat treatment on Tg, Tm and crystallinity of the polymer are evaluated at different heating temperatures.
The experimental results showed that mostly loose chains (sol fraction) contribute to the crystallinity of the polymer.
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The crystalline structure and relative crystallinity of the polymers were examined by wide-angle X-ray diffraction (WAXD) using an EMPYREAN diffractometer system (PANanalytical, Netherlands) equipped with a filtered Cu K α radiation source (λ = 1.540598 Å) and a PIXcel3D detector.
The crystallinity of the polymers was studied by DSC analysis.
The alkyl substituent influenced some properties such as solubility, thermal stability, glass transition and crystallinity of the polymers.
The crystallinity of the polymers synthesized from the high crystallinity prepolymer was significantly higher than for those synthesized from the low crystallinity prepolymer.
The results show that the alkylthio-thiophene/selenophene side groups on BDT unit and intramolecular hydrogen bonding interaction in DPP acceptor unit play important roles in affecting the absorption, HOMO energy levels, molecular planarity and the crystallinity of the polymers.
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