High-density polyethylene (HDPE) has a higher strength-to-density ratio and stiffness but a low branching degree for the packed linear chains that restrict the ability to bond and resist cracking. This study conducts the role of inserting rigid nanoclay (NC) and soft acrylonitrile butadiene styrene (ABS) on the structural, nonlinear fracture toughness and crack resistance of a ternary HDPE/low-density polyethylene-grafted maleic anhydrite (LDPE-g-MA)/ABS blend. Varying additions of 1, 3, 5, and 7 % NC and 5, 10, 15 wt. % ABS were inserted into neat HDPE and HDPE90/LDPE-g-MA10. All materials were hand-mixed before feeding into a single screw extruder and directly melt-blended twice to achieve a good dispersion of nanofiller in the matrix. The structural characteristics and the fracture surfaces of NC/HDPE/LDPE-g-MA and NC/HDPE/LDPE-g-MA/ABS were investigated by TEM, XRD, SEM, and FTIR spectra. Tensile strength and the critical dissipated energy (JIc) determined by quasi-static J-integral fracture mechanic revealed a higher absorbing fracture energy of 75 KJ/m2 for the binary and 85 KJ/m2 for the ternary nanocomposites. The synergistic percolated role of the NC particles and ABS copolymer in front of the crack tip region hinders crack growth for the presence of micro-void coalescence and massive shear-yielding toughening mechanisms.