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The visible temperature difference between the laid-up tow and its surface underneath is analyzed and information of lay-up defects such as overlaps, gaps, twisted tows and bridging derived.
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We analysed similar spots that were visible in soluble protein extracts obtained from cells that had been grown at optimal growth temperature and subjected to heat treatment for 30 min. This was done to ensure that the visible temperature-dependent changes in Ser/Thr phosphorylation referred to the same protein(s).
The visible room temperature PL spectrum of the annealed nanofibers demonstrates an increase in luminescent intensity, and the low temperature (15 K) PL spectrum presents two new PL peaks (400 and 540 nm) when compared to bulk GaSb.
Comparing all the conditions, the significant effect of residence time on the formation of S units is clearly visible while temperature might play a minor role.
Note that the charged exciton is still visible at temperatures much higher than is seen in other quasi-2D systems such as GaAs QWs29.
The onset of crystallization is visible at temperatures as high as 170°C, which is far above the crystallization range under quiescent conditions.
Back wall reflections were clearly visible at temperatures up to 900 °C on stainless and ferromagnetic low carbon steel, enabling wall thickness to be measured, taking into account thermal expansion of the sample.
In addition, a visible room-temperature phosphorescence (RTP) signal occurs along with the photolysis reaction as the suppression of intramolecular photoinduced electron transfer (PET) process from the anthracene moiety to phosphorous 6-bromoisoquinoline moiety.
PS has been widely explored for its strong visible room-temperature photoluminescence (PL) and for its high potential application in photovoltaics (PV [1, 2].
Silicon nanoparticles extracted from highly porous silicon (Si-ncs) showing visible room-temperature luminescence have been suggested to be used, e.g. as fluorescent labels, biological sensors, photoresponsive systems for regulated drug delivery or scaffold for various tissues [2 5].
Hereby, the intensity drop is slower than for the QW the QW is hardly visible for temperatures over 150 K, whereas we can identify the weaker optical response of the MGS-S and the MGS-D structures up to 190 K.
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