Abstract:In this study, a fast and convenient method that can characterize the molecular weight (MW) and its distribution (PDI) of polyamide 1012 after the solid-state polymerization (SSP) was proposed with the rheological technique. Conventionally, polyamides have to be chemically modified to become soluble in an organic solvent suitable for the Gel Permeation Chromatography (GPC) measurement. Herein, to avoid the complex operation of chemical modifica-
“…Long-chain PAs (LCPAs) refer to an emerging family of PAs in which the number of methylene groups between adjacent amide groups in the main chain is no less than 10. , Some advantages of LCPAs over conventional PAs (such as PA6 and PA66) attributed to the relatively long methylene segments include good dimensional stability, excellent low-temperature performance, and high processability. − Thus, LCPAs have been widely used in automotive manufacturing and electronic applications. PA1012 is a kind of typical AABB-type even–even LCPA, and it has been developed in recent decades.…”
In this study, the crystal form transition
and semicrystalline
morphology evolution of quenched polyamide 1012 (PA1012) during heating
were investigated. Quenched PA1012 displayed a pseudohexagonal γ′
form at room temperature, in which the methylene segments adopted
a trans conformation, the methylene group directly
attached to the amide group was twisted, and the hydrogen bonding
pointed in all directions. During heating, the γ′ form
gradually transformed into the γ form as the trans methylene sequences that are away from the amide group further twisted,
and the dihedral angle between the amide and methylene plane exhibited
a narrow distribution. The transition onset temperature was near the
glass transition temperature of quenched PA1012. The semicrystalline
morphology of quenched PA1012 was characterized as a loose network
consisting of a disordered arrangement of thin lamellae with poorly
defined boundaries. As the annealing temperature increased, the lamellae
became more perfect and thicker, while the morphological type remained
the same.
“…Long-chain PAs (LCPAs) refer to an emerging family of PAs in which the number of methylene groups between adjacent amide groups in the main chain is no less than 10. , Some advantages of LCPAs over conventional PAs (such as PA6 and PA66) attributed to the relatively long methylene segments include good dimensional stability, excellent low-temperature performance, and high processability. − Thus, LCPAs have been widely used in automotive manufacturing and electronic applications. PA1012 is a kind of typical AABB-type even–even LCPA, and it has been developed in recent decades.…”
In this study, the crystal form transition
and semicrystalline
morphology evolution of quenched polyamide 1012 (PA1012) during heating
were investigated. Quenched PA1012 displayed a pseudohexagonal γ′
form at room temperature, in which the methylene segments adopted
a trans conformation, the methylene group directly
attached to the amide group was twisted, and the hydrogen bonding
pointed in all directions. During heating, the γ′ form
gradually transformed into the γ form as the trans methylene sequences that are away from the amide group further twisted,
and the dihedral angle between the amide and methylene plane exhibited
a narrow distribution. The transition onset temperature was near the
glass transition temperature of quenched PA1012. The semicrystalline
morphology of quenched PA1012 was characterized as a loose network
consisting of a disordered arrangement of thin lamellae with poorly
defined boundaries. As the annealing temperature increased, the lamellae
became more perfect and thicker, while the morphological type remained
the same.
The pseudohexagonal γ′ phase of polyamide
1012 can
be obtained by melt-quenching and gradually transformed into the γ
form during heating, in which the trans methylene
segments away from the amide group are further twisted. What happens
during uniaxial stretching? In this work, the multistage structural
evolution of the γ′ phase during uniaxial stretching
has been studied by using in situ wide-angle X-ray scattering (WAXS)
and Fourier transform infrared spectroscopy (FTIR). The multistage
conformational evolution of the γ′ phase during stretching
was studied by quantitative analysis of the infrared progression bands
and was found to be closely correlated with the mechanical response
during tensile deformation. In the yield stage, the twisted methylene
segments in the initial γ′ phase undergo conformational
ordering under stress activation, and the γ′ phase spontaneously
transforms into a defective α phase. Furthermore, in the plateau
stage, strain induces significant conformational disorder and the
transient α phase transforms into the most conformationally
disordered γ phase. Finally, at the strain hardening stage,
the reversible crystal form transition from the γ phase to the
regular γ′ phase is induced by stress, accompanied by
an obvious conformational ordering process. The stress- and strain-induced
conformational torsional motions are found to be completely opposite,
with the former inducing conformational order and the latter inducing
conformational disorder.
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