Interfaces generation via severe plastic deformation – a new way to multiple shape memory polymer composites

The deposited data contain results obtained from measurements: DSC, DMA, WAXS, NMR, shape memory effect tests.The attached data are provided in the form of text files as well as source files typical for the respective software used.The attached data were obtained using the following instruments: The thermomechanical properties were characterized using a Q800 DMA (TA Instruments, New Castle, DE, USA) and differential scanning calorimeter DSC Q20 (TA Instruments, New Castle, DE, USA). The X-ray measurements were performed with a Aeris XRD diffractometer (Malvern Panalytical) operating at 40 kV and 7.5 mA. The phase mixing efficiency of polymers was investigated by 1H spin-lattice relaxation time measurements both in the laboratory and in rotating frames (T1, T1ρ) using solid-state 13C crosspolarization magic-angle spinning NMR experiments. NMR data were obtained using the Bruker AVANCE III WB 400 NMR spectrometer. Thermally-activated shape memory characterization of samples was conducted using Q800 DMA instrument with the film tension clamp under controlled strain and controlled force modes.