Thermal characterization and solid-state13C-NMR investigation of blends of poly(N-phenyl-2-hydroxytrimethylene amine) and poly(N-vinyl pyrrolidone)

Compatibility study in poly(tetramethyleneadipate‐co‐terephthalate)/polystyrene bioblends

“…In many instances, such an outcome is considered as corroborating evidence for a phase‐separated, and immiscible, blend. (c) The thermal stability of the blend is intermediate between those of the components 40–47. This observation could imply an improvement, worsening, or no change in the thermal stability as a result of blending.…”

Compatibility study in poly(tetramethyleneadipate‐co‐terephthalate)/polystyrene bioblends

“…In many instances, such an outcome is considered as corroborating evidence for a phase‐separated, and immiscible, blend. (c) The thermal stability of the blend is intermediate between those of the components 40–47. This observation could imply an improvement, worsening, or no change in the thermal stability as a result of blending.…”

Morphology and miscibility of chitosan/soy protein blended membranes

“…The solid state NMR spectra were recorded on Bruker DRX spectrometers operating at a 1 H frequencies of 400 and 500 MHz. Proton spin-lattice relaxation time (T H 1 ) values were determined using a 1 H-13 C cross-polarization (CP) inversion recovery sequence (Zhong & MI, 1999) and by fitting the 13 C peak intensities to a single exponential.…”

Compatibility study in poly(tetramethyleneadipate‐co‐terephthalate)/polystyrene bioblends

“…In many instances, such an outcome is considered as corroborating evidence for a phase‐separated, and immiscible, blend. (c) The thermal stability of the blend is intermediate between those of the components 40–47. This observation could imply an improvement, worsening, or no change in the thermal stability as a result of blending.…”

Morphology and miscibility of chitosan/soy protein blended membranes

“…The solid state NMR spectra were recorded on Bruker DRX spectrometers operating at a 1 H frequencies of 400 and 500 MHz. Proton spin-lattice relaxation time (T H 1 ) values were determined using a 1 H-13 C cross-polarization (CP) inversion recovery sequence (Zhong & MI, 1999) and by fitting the 13 C peak intensities to a single exponential.…”

Compatibility study in poly(tetramethyleneadipate‐co‐terephthalate)/polystyrene bioblends

“…In many instances, such an outcome is considered as corroborating evidence for a phase‐separated, and immiscible, blend. (c) The thermal stability of the blend is intermediate between those of the components 40–47. This observation could imply an improvement, worsening, or no change in the thermal stability as a result of blending.…”

Morphology and miscibility of chitosan/soy protein blended membranes

“…The solid state NMR spectra were recorded on Bruker DRX spectrometers operating at a 1 H frequencies of 400 and 500 MHz. Proton spin-lattice relaxation time (T H 1 ) values were determined using a 1 H-13 C cross-polarization (CP) inversion recovery sequence (Zhong & MI, 1999) and by fitting the 13 C peak intensities to a single exponential.…”