IntroductionPoly(ethylene terephthalate) (PET) is a semicrystalline polymer with excellent chemical resistance, thermal stability, and spinnability. Due to its low cost and high performance, PET is in widespread use in our modern life, ranging from textile fibers, films, bottles containers and food packaging materials to engineering plastics, etc. However, numerous shortcomings such as low rate of crystallization, long cycle times for injection moulding, low melt strength and low distortion temperature limit its application [1,2]. To meet the practical needs and improve its performance, the addition of inorganic filler into PET matrix has been a research focus, and dramatic enhancements in properties such as their mechanical, gas barrier property and thermal property can be achieved [3][4][5][6][7][8][9][10][11][12][13]. These enhancements result from homogeneous dispersion of nanoparticles in polymer matrix and the interaction between the nanoparticles and PET matrix. The in situ polymerization technique is particularly attractive, which enables to exercise control over both the polymer architecture and the final structure of the composites. Recently various nanoparticles have been applied in the preparation of PET nanohybrids via in situ polymerization or melt mixing, including layered silicates montmorillonite (MMT) [3][4][5][6], spherical silica [7,8] Abstract. Poly(ethylene terephthalate) (PET) nanocomposites containing rod-like silicate attapulgite (AT) were prepared via in situ polymerization. It is presented that PET chains identical to the matrix have been successfully grafted onto simple organically pre-modified AT nanorods (MAT) surface during the in situ polymerization process. The covalent bonding at the interface was confirmed by Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The content of grafted PET polymer on the surface of MAT was about 26 wt%. This high grafting density greatly improved the dispersion of fillers, interfacial adhesion as well as the significant confinement of the segmental motion of PET, as compared to the nanocomposites of PET/pristine AT (PET/AT). Owing to the unique interfacial structure in PET/MAT composites, their thermal and mechanical properties have been greatly improved. Compared with neat PET, the elastic modulus and the yield strength of PET/MAT were significantly improved by about 39.5 and 36.8%, respectively, by incorporating only 2 wt % MAT. Our work provides a novel route to fabricate advanced PET nanocomposites using rod-like attapulgite as fillers, which has great potential for industrial applications.