2021
DOI: 10.3390/ma14040730
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Glass Transition Behavior of Wet Polymers

Abstract: We have performed a systematical investigation on the glass transition behavior of amorphous polymers with different solvent concentrations. Acrylate-based amorphous polymers are synthesized and treated by isopropyl alcohol to obtain specimens with a homogenous solvent distribution. The small strain dynamic mechanical tests are then performed to obtain the glass transition behaviors. The results show that the wet polymers even with a solvent concentration of more than 60 wt.% still exhibit a glass transition b… Show more

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Cited by 9 publications
(7 citation statements)
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“…The CGG + PolyOX thermogram did not show a Tg. Thus, it can be inferred that the addition of PolyOX in the absence of the crosslinker generates an HG with higher crystallinity, considering that the Tg is usually a characteristic presented by amorphous or semi-crystalline materials [ 19 ]. On the other hand, for peak 3, the Tm decreases for CL CGG, increases in CGG + PolyOX, and decreases again in CGG-PolyOX but above CL CGG; this same behavior was presented for Td in peak 4.…”
Section: Resultsmentioning
confidence: 99%
“…The CGG + PolyOX thermogram did not show a Tg. Thus, it can be inferred that the addition of PolyOX in the absence of the crosslinker generates an HG with higher crystallinity, considering that the Tg is usually a characteristic presented by amorphous or semi-crystalline materials [ 19 ]. On the other hand, for peak 3, the Tm decreases for CL CGG, increases in CGG + PolyOX, and decreases again in CGG-PolyOX but above CL CGG; this same behavior was presented for Td in peak 4.…”
Section: Resultsmentioning
confidence: 99%
“…The amount of diffused second polymer chains in the PMMA cores is calculated on the basis of the difference between the peak area of the PMMA core and the peak area of the deconvoluted peak associated with the PMMA for composite particles in the derivate graphs of C p in Figure f–j (see the Supporting Information). The percentage of diffused polymers versus the difference between T g of the water-saturated polymer ( T gw ) , and T r (Δ T = T gw – T r ) is presented in Figure . It can be clearly seen that the percentage of diffused polymers decreases as the Δ T increases, and the maximum polymer chain diffusion happens for the sample with PnBA as the second polymer, which is about 40%; so, all samples have the CS structure.…”
Section: Resultsmentioning
confidence: 99%
“…For the cases of Figure 5d, laminates have two glassy states before reached to a rubbery state. The first T g was occurred due to prolonged moisture absorption which acts as a plasticizer that was a case on reducing hydrogen bond, Van der Waals forces and hardness of the laminates [27,28]. In those figures, the response on E of all laminates was similar at 1 Hz and 10 Hz.…”
Section: Dma Testsmentioning
confidence: 88%