An in-situ compatibilized starch (St) and polyacrylonitrile (PAN) composite spinning solution was designed by preparing starch-graft-polyacrylonitrile (St-g-PAN) through graft copolymerizing acrylonitrile from soluble starch and using ammonium cerium nitrate (CAN) as initiator. As dimethyl sulfoxide (DMSO) was used as the solvent, St/St-g-PAN/PAN/DMSO spinning solution was prepared and St/St-g-PAN/PAN composite fibers were obtained by dry-wet spinning technique. The effects of air gap, coagulation bath, hot drawing and stretching, and thermal-setting process were studied in detail. Fourier transform infrared spectroscopy (FT-IR), solid state nuclear magnetic resonance (C NMR), thermogravimetric analysis (TGA), X-ray diffraction analysis (XRD), and scanning electron microscopy (SEM) were used to characterize the structure and morphology of the copolymer and the fibers. Single fiber strength tester and sonic orientation instrument were performed to measure the fiber mechanical properties and orientation degrees. The results showed that as the grafting ratio ~150.0% and the reacting mixture containing St ~9.8%, St-g-PAN ~81.6%, and homo-PAN ~8.6% in DMSO solution with 6.0 wt% in concentration were used, the spinning parameters such as air gap ~35 mm, coagulation bath concentration ~70%, temperature ~25 °C, and positive stretching ~48%, hot drawing and stretching 6 times at 80 °C, thermal-setting at 90 °C for 3 h under constant length mode were met, composite fibers with breaking strength 3.41 cN·dtex, breaking elongation 14.41%, sonic orientation factor 0.625, moisture recovery ratio 10.53% under standard condition (1 atm, 22 °C, and relative humidity 65%), and boiling water shrinkage ratio 9.60% were obtained. The as prepared composite fiber was better than common viscose fiber 2.11 cN·dtex and cotton fiber ~3.24 cN·dtex and expected to be used in the fields of medical gauze, bandage, protective clothing, et al. besides of common textiles. The in-situ compatibilization method can be applied in preparation of other composite polymer materials.
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http://dx.doi.org/10.1016/j.ijbiomac.2022.05.091 | DOI Listing |
Int J Biol Macromol
December 2024
College of Materials Science and Engineering, Nanjing Tech University, Nanjing 211816, Jiangsu Province, China. Electronic address:
Over the past decades, emerging bioplastics have attracted much interest from the scientific and industrial communities because of public concerns about environmental problems and sustainable development. In this study, poly(lactic acid) (PLA) was toughened by ductile biodegradable poly(butylene adipate-co-terephthalate) (PBAT) and biosourced plasticizer epoxidized linseed oil (ELO), and a chain-extending agent (CEA) was added to promote the compatibility and toughness of the bio-blends. It was shown that "in situ" grafted polymers were created in the bio-blends with the aid of CEA, greatly enhancing the compatibility and ductility of the compatibilized blends.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Microcellular Plastics Manufacturing Laboratory, Department of Mechanical and Industrial Engineering, University of Toronto, Toronto, Ontario M5S 3G8, Canada.
In this study, we proposed a novel technique to simultaneously enhance the oxygen barrier properties and stiffness of high-density polyethylene (HDPE) while preserving its ductility. By utilizing in situ nanofibrillation, fiber-in-fiber composites of an HDPE matrix and ethylene-vinyl alcohol (EVOH) nanofibers were fabricated. Due to the high interfacial tension between HDPE and EVOH, stemming from their differences in chemical structure and polarity, styrene/ethylene-butylene/styrene copolymer grafted with maleic anhydride (SEBS--MA) was used as a compatibilizer to improve the affinity between the two polymers.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
School of Materials Science and Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, China. Electronic address:
Enhancing the ductility of polylactide (PLA) through toughening modification to expand the application range of PLA aligns with the requirements of green development. In this study, eco-friendly bio-based plastic polyamide 11 (PA11) was chosen to modify poly(l-lactide) (PLLA). PA11 and poly(d-lactide) (PDLA) were grafted onto the main chain of ADR via simple reactive processing and utilized as reactive compatibilizers to improve toughening efficiency of PA11.
View Article and Find Full Text PDFPolymers (Basel)
October 2024
State Key Laboratory of Polymer Materials Engineering, Polymer Research Institute of Sichuan University, Chengdu 610065, China.
Replacing traditional disposable, non-biodegradable plastic packaging with biodegradable plastic packaging is one of the key approaches to address the issue of "white pollution". PBAT/PLA/inorganic filler composites are widely utilized as a biodegradable material, commonly employed in the field of packaging films. However, the poor dispersion of inorganic fillers in the polymer matrix and the limited compatibility between PBAT and PLA have led to inferior mechanical properties and elevated costs.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
Key Laboratory of Special Functional Aggregated Materials (Shandong University), Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.
Polymer blending has been an important method to create materials with specific properties that have synergistic effects. However, there are few reports on the mechanism of synergistic effects. It is well known that it is quite difficult to obtain ideal blends composed of nonpolar organosilicon polymers and polar polymers.
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