Nano-ZnO particle （nZnOp） reinforced polyethylene glycol （PEG）/polyethylene terephthalate （PET） （nZnOp/PEG/PET） copolymeric composites with different mass fractions and molecular weights of PEG are synthesized...Nano-ZnO particle （nZnOp） reinforced polyethylene glycol （PEG）/polyethylene terephthalate （PET） （nZnOp/PEG/PET） copolymeric composites with different mass fractions and molecular weights of PEG are synthesized via in-situ polymerization. The dispersion of nZnOp in copolymer matrixes and the effects of PEG and nZnOp particles on the crystallization behavior of the composites are studied by TEM, differential scanning calorimetry（DSC）, XRD and Fourier thansform infrared spectroscopy （FTIR ）. The results reveal that nZnOp particles are dispersed in the matrixes with nano-scale, and the addition of PEG induces more homogeneous dispersion of nZnOp. Simultaneously, these nanoparticles become nucleating centers during the crystallization of the matrixes. PEG segments can improve the flexibility of the PET molecular chain, resulting in the drop of the cold crystallization temperature and the rise of the crystallization rate of the composites. Furthermore, PEG （4 000） with the mass fraction of 10% can promote the crystallization rate of the composites. The mechanical properties show that the nano-particles strengthen and toughen the PET matrix, whereas PEG weakens these improve- ments.展开更多
Polyethylene terephthalate(PET)fibers are the largest category of chemical fibers and are widely used.However,the dyeing of PET fibers requires high temperature and pressure(130℃and 0.2 MPa),and the dyeing process co...Polyethylene terephthalate(PET)fibers are the largest category of chemical fibers and are widely used.However,the dyeing of PET fibers requires high temperature and pressure(130℃and 0.2 MPa),and the dyeing process consumes huge amounts of energy.Existing studies have shown that the dyeing ability of PET is directly related to the size of the amorphous region,which determines the external conditions for dyeing.In this research,we synthesized a series of low-temperature easydyeing masterbatches,PET-co-polyethylene glycol(PETEG),using polyethylene glycol(PEG)with different number-average molecular masses Mn and additive amounts.The phase domain size of the amorphous region of PET fibers was regulated via the masterbatch method.The relationship between the phase domain size and dyeing performance was explored from three perspectives:the amount of masterbatch,type of masterbatch,and PEG relative molecular mass.The results indicate that the fiber sample with PEG(Mn=2000 g/mol)at a mass fraction of 20%modified masterbatch has a smaller crystalline lamellar thickness(5.59 nm)and a larger interlamellar amorphous layer thickness(6.43 nm).The increase in the long period and lamellar inclination angle results in a looser structure,allowing small molecule dyes to diffuse into the fibers more easily.The dye-uptake increases from 63.21%to 92.66%at 100℃with the addition of the masterbatch.Additionally,the dye-uptake of the modified fibers increases with the relative molecular mass of PEG and the mass fraction of the masterbatch.All modified fibers achieve a staining color fastness of grade 4 or higher.This research demonstrates a simple masterbatch method that enables atmospheric pressure dyeing and provides a practical solution for efficient,low-temperature,and low-energy dyeing of PET fibers.展开更多
基金Supported by the Program of Jiangsu Development & Reform Commission(2005)the Industrial-ization Boosting Program of College Scientific Reserach Achievements of the Education Department of Jiangsu Province(JHB06-03)~~
文摘Nano-ZnO particle （nZnOp） reinforced polyethylene glycol （PEG）/polyethylene terephthalate （PET） （nZnOp/PEG/PET） copolymeric composites with different mass fractions and molecular weights of PEG are synthesized via in-situ polymerization. The dispersion of nZnOp in copolymer matrixes and the effects of PEG and nZnOp particles on the crystallization behavior of the composites are studied by TEM, differential scanning calorimetry（DSC）, XRD and Fourier thansform infrared spectroscopy （FTIR ）. The results reveal that nZnOp particles are dispersed in the matrixes with nano-scale, and the addition of PEG induces more homogeneous dispersion of nZnOp. Simultaneously, these nanoparticles become nucleating centers during the crystallization of the matrixes. PEG segments can improve the flexibility of the PET molecular chain, resulting in the drop of the cold crystallization temperature and the rise of the crystallization rate of the composites. Furthermore, PEG （4 000） with the mass fraction of 10% can promote the crystallization rate of the composites. The mechanical properties show that the nano-particles strengthen and toughen the PET matrix, whereas PEG weakens these improve- ments.
基金Key R&D Program of the Xinjiang Uygur Autonomous Region,China(No.2024B01011)。
文摘Polyethylene terephthalate(PET)fibers are the largest category of chemical fibers and are widely used.However,the dyeing of PET fibers requires high temperature and pressure(130℃and 0.2 MPa),and the dyeing process consumes huge amounts of energy.Existing studies have shown that the dyeing ability of PET is directly related to the size of the amorphous region,which determines the external conditions for dyeing.In this research,we synthesized a series of low-temperature easydyeing masterbatches,PET-co-polyethylene glycol(PETEG),using polyethylene glycol(PEG)with different number-average molecular masses Mn and additive amounts.The phase domain size of the amorphous region of PET fibers was regulated via the masterbatch method.The relationship between the phase domain size and dyeing performance was explored from three perspectives:the amount of masterbatch,type of masterbatch,and PEG relative molecular mass.The results indicate that the fiber sample with PEG(Mn=2000 g/mol)at a mass fraction of 20%modified masterbatch has a smaller crystalline lamellar thickness(5.59 nm)and a larger interlamellar amorphous layer thickness(6.43 nm).The increase in the long period and lamellar inclination angle results in a looser structure,allowing small molecule dyes to diffuse into the fibers more easily.The dye-uptake increases from 63.21%to 92.66%at 100℃with the addition of the masterbatch.Additionally,the dye-uptake of the modified fibers increases with the relative molecular mass of PEG and the mass fraction of the masterbatch.All modified fibers achieve a staining color fastness of grade 4 or higher.This research demonstrates a simple masterbatch method that enables atmospheric pressure dyeing and provides a practical solution for efficient,low-temperature,and low-energy dyeing of PET fibers.
