“…6 Later, ultrasonically aided processing was used to prepare various polymer blends, including high-density polyethylene (HDPE)/polystyrene (PS), 7,8 polypropylene (PP)/PS, 9 PP/ethylene propylene diene methylene (EPDM) rubber, [10][11][12][13][14][15][16] PP/natural rubber (NR), 10,11,17 HDPE/NR, 10,11 HDPE/ EPDM, 10,11 HDPE/styrene butadiene rubber (SBR), 10,11 NR/SBR, 10,11 PP/ultrahighmolecular weight polyethylene, 18 linear low-density polyethylene (LLDPE)/lowdensity polyethylene, 19,20 HDPE/polyamide 6 (PA6), 21 PS/EPDM, 22,23 PP/PA6, 24 poly(lactic acid)/poly(butylene adipate-co-terephthalate), 25 ethylene-a-olefin copolymers (POE)/PS, 26 PA6/POE/POE grafted with maleic anhydride (POE-g-MAH), 27 LLDPE/POE, 28 polyethylene terephthalate (PET)/LCP, 29 polyethylene naphthalate (PEN)/liquid crystalline polymers (LCP), 30 PET/PEN, 31 blends of two different LCPs. 32 Most articles reported the in situ copolymerization of polymers by the ultrasonic treatment, as patented by Isayev and Hong. 33 The Fourier transform infrared (FTIR) analysis of HDPE/PS, 7 PP/PS, 9 PP/EPDM, 14,16 and PS/EPDM 22 blends prepared by ultrasonic treatment showed the presence of chemical structure of the dissolved polymer phas...…”