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Adding a Zn2+ ion not only caused partial fluorescence quenching but also induced a broad emission peak in the range of 525 700 nm.
Updraft speeds typically peak in the range of 5 to 10 metres (16 to 33 feet) per second, and speeds exceeding 20 metres (66 feet) per second are common in the upper parts of large storms.
The results show: (1) pore refinement by GGBS is evident and GGBS increases substantially the SSA and fractal dimension values; (2) the pore refinement moves pore distribution from the range of 10 nm–100 nm to that of <10 nm; (3) the self-desiccation under sealed-curing creates a PSD peak in the range of >100 nm and compacts the nanostructure of hydrates.
A broad peak in the range of 20 23° is due to amorphous silica [29, 30].
Moreover, FTIR spectrum exhibited Pb O bond peak in the range of 400 530 cm−1.
Rh/Al2O3 exhibited a reduction peak in the range of 50 300 °C ascribing to the reduction of Rh3+ → Rh0.
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The characteristic G-mode peak at around 1590 cm−1 and the radial breathing mode (RBM) peaks in the range of 120 230 cm−1 indicate that the fibrous substances formed are SWCNTs.
In the photoluminescence (PL) spectrum of (TPAT 3 film, there are no excimer emission peaks in the range of 400 550 nm region as those of TAPC and TTA.
Ionic aggregation is further confirmed by the occurrence of two closely spaced melting peaks in the range of 322 328 and 361 365 °C in differential scanning calorimetry analysis.
The data in Table 1 shows the XRD peaks in the range of 2θ = 4° 70°.
Similarly, aldehydic C=O bond displayed the peaks in the range of 1683 1699 cm−1 in different esters.
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