Composites from Renewable and Sustainable Materials by Matheus Poletto

By Matheus Poletto

Composites from Renewable and Sustainable fabrics comprises 16
chapters written by means of foreign material specialists investigating
the attribute and present software of fabrics from renewable
and sustainable sources.
The reader will increase a deeper figuring out concerning the concepts
related to renewable fabrics, biomaterials, normal fibers,
biodegradable composites, starch, and recycled fabrics. This book
will function the start line for fabrics technological know-how researchers,
engineers, and technologists from the various backgrounds in physics,
chemistry, biology, fabrics technological know-how, and engineering who wish to
know and higher comprehend the basic features and current
applications of renewable and sustainable fabrics in several
applications.

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Specimens were removed from the water, wiped dry with tissue paper and measured. The percentages of water absorption (WA) and thickness swelling (TS) were calculated using Eqs. 1 and 2: WA (%) = TS(%) = Wt - W0 ´ 100 W0 Tt - T0 ´ T0 100 (1) (2) where W0 and Wt represent the oven-dry weight (the initial weight) and weight after water exposure at time t, respectively, whereas T0 and Tt represent the oven-dry thickness and thickness after water exposure at time t, respectively. Three replicates of specimens were tested for each formulation to obtain the average results.

States of water in different hydrophilic polymers—DSC and FTIR studies. Polymer. 2001;42:8461–7. 1016/ S0032-3861(01)00358-5 [6] Scida D, Assarar M, Poilâne C, Ayad R. Influence of hygrothermal ageing on the damage mechanisms of flax-fibre reinforced epoxy composite. Composites Part B: Engineering. 2013;48:51–8. 010 [7] Shen CH, Springer GS. Moisture absorption and desorption of composite materials. Journal of Composite Materials. 1976;10:2–20. 1177/002199837601000101 [8] Fávaro SL, Lopes MS, De Carvalho Neto AGV, De Santana RR, Radovanovic E.

This process occurred because the neat polymer blend comprised a series of interchained monomers, where an increase of temperature promoted the random chain scission through thermal degradation and depolymerization (at Td) [22]. The lower Td for CTPB than that of UTPB was due to an increase of rHDPE-rPET interaction because of the addition of E-GMA compatibilizer which possessed a lower decomposition temperature [23]. Figure 12. TGA thermogram data: (a) main decomposition temperature (Td) of polymer component and (b) residues after 600 °C for TPB/RHB biocomposites.

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