Crystal structure and thermodynamic parameters of Nylon‐1010

Publisher Website
Google Scholar
Abstract
WAXD, SAXS, FTIR, DSC and density techniques have been used to investigate the crystal structure, crystal density ρc, amorphous densitypaequilibrium heat of fusion δH°mand equilibrium melting temperatureT°m. By extrapolating the straight lines in the FTIR absorbance against density plot to zero intensity. ρcand ρawere estimated to be 1.098 and 1.003 g/cm3respectively. The ρcobtained was too low in value. From X‐ray diffraction patterns of uniaxially oriented fibres, the crystal structure of Nylon‐1010 was determined. The Nylon‐1010 crystallized in the triclinic system, with lattice dimensions:a= 4.9 Å,b= 5.4 Å,c= 27.8 Å, α = 49°, β = 77°, γ = 63.5°. The unit cell contained one monomeric unit, the space group was P1, and the correct value of ρcwas 1.135 g/cm3. The degree of crystallinity of the polymer was determined as about 60% (at RT) using Ruland's method.SAXS has been used to investigate the crystalline lamellar thickness, long period, transition zone, the specific inner surface and the electron density difference between the crystalline and amorphous regions for Nylon‐1010. The analysis of data was based upon a one‐dimensional electron‐density correlation function. δH°mwas estimated to be 244.0 J/g by extrapolation of δH°min the plot of heat of fusion against specific volume of semicrystalline specimens to the completely crystalline condition (V= 1/ρc). Owing to the ease of recrystallization of melt‐crystallized Nylon‐1010 specimens, the well‐known Hoffman'sTm‐Tcmethod failed in determiningT°mand a Kamide double extrapolation method was adopted. TheT°mvalue so obtained was 487 K.

This publication has 11 references indexed in Scilit: