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PLA nanocomposites are prepared by us, and to better develop the function of silica nanoparticle, the surface of silica nanoparticles are modified by introducing PLA chains via "grafting to" method in our research. According to the results of ¹H NMR and TGA, it shows that the PLA grafted Silica nanoparticles are successfully synthesized by controlling the reaction condition, and the molecular weight of the grafted PLA chains is relatively as high as 22 400 g/mol. PLA Nanocomposites with modified nanoparticles are prepared using a convenient melt blending method to guarantee well-distribution of the particles. The well-dispersion state of silica nanospheres is confirmed by Scan Electrical Micrograph (SEM) technology. From the dynamic shear rheology tests, the strain and time sweep both reveal that stability networks are formed in these nanocomposites. And the frequency sweep shows that the nanoparticles with long grafted chains dramatically enhanced the storage and viscosity of the pure PLA. The rheology testing suggests that strong particle-matrix interactions between molecularly/nano-level dispersed grafted silica and PLA chains formed; and the elongational viscosity of PLA has been markedly improved with the addition of the nanoparticle. The effect of modified nanoparticles on the thermal properties of PLA has also been studied by us using Differential Scanning Calorimetry (DSC). It reveals that the crystallization rate of PLA has been improved as the long grafted chains play as the nucleation sites for PLA. Finally based on these rheology and crystallization researches, the nanocomposites are used to prepare PLA blowing films. Compared to pure PLA and PLA/unmodified silica nanocomposites, the results show that the stability of the film blowing has been greatly improved and the blow-up ratio has been increased with the addition of PLA grafted nanoparticles. The modified nanoparticles hold significant candidates to improve the thermal stability and the processability of pure PLA, especially used as special processing agent in the field of PLA stretch shaping process. [ABSTRACT FROM AUTHOR]

Nowadays natural fiber, used in reinforced composites, is widely concerned. However, no natural fiber reinforced reactive thermoplastic polymer grades had been prepared so far. Through our studies, it was demonstrated that there was a severe retardation and discoloration occurred in the reactive processing between anionic polyamide-6 (APA-6) and natural fiber, which result in incomplete polymerization when put together. In order to solve the problem, two methods were adopted in this paper, which are fiber pretreatment and usage of a new-style initiator called caprolactam magnesium bromide. The former is to remove sizing agent and impurities on the surface of fiber, and the latter is to weaken the side reactions between APA-6 and natural fiber by the nature of its lower reactivity and weaker alkaline. In cooperation with both methods, the severe retardation and discoloration had been improved significantly, so that the polymerization of APA-6 in natural fiber was occurred smoothly. Following textile-natural fiber reinforced APA-6 composites with an average thickness of 2.5 mm and a fiber volume content of 50% was prepared by vacuum assisted resin transfer molding (VARTM). The soxhlet extraction, dilute solution viscometry and differential scanning calorimeter (DSC) measurements respectively suggested the degree of conversion, viscosity-average molar mass and crystallization of composites was up to 94%, 11.3×104 and 50%. Remarkable improvement of mechanical properties were achieved through dynamic mechanical analysis (DMA), tensile and three-point bending test. Favorable interfacial adhesion and wettability were revealed by scanning electron microscopy (SEM) observation. Therefore, all of the above good performance make this new-style and environmentally friendly composites have broad application prospects. [ABSTRACT FROM AUTHOR]