of polymers into fibers. [2-8] During this alignment process, a material with often mediocre bulk properties is transformed into significantly stiffer and stronger highperformance polymeric fiber with a broad range of high-end applications. [6,9,10] Given its relative simple structure and flexible nature, considerable attention was spend on polyethylene. [4,11-16] Years of research and industrial development have resulted in two prevailing processing techniques: melt-spinning and gel-spinning. [2,6] During melt-spinning, the polymer melt is extruded and cooled just below the melting temperature. Subsequently the polymer is drawn in the solid-state up to its maximal attainable draw ratio. This process allows for the fabrication of high density polyethylene (HDPE) fibers with Young's moduli of up to 50-70 GPa and tensile strengths of 0.8-1.4 GPa. [1,17-19] The meltspinning and solid-state drawing process has two major drawbacks which are strongly linked to the molecular weight. Melt-spinning is restricted to lower molecular weights (<200 kg mol −1) due to a strong increase in viscosity induced by chain slip between entanglements. The increase of viscosity in polymer (solutions) is typically described via the scaling of zero shear viscosity, where polymers with a molecular weight above the critical molecular weight at which entanglements can form (, 2•) c e ∝ ≤ ≥ M M M M M M (1) in which ϕ indicates the volume fraction of polymer in solution. Equation (1) makes apparent that an increase in molecular weight comes at the expense of a steep increase in viscosity which, however, can be compensated for by diluting with a solvent. Second, given the molecular weight between entanglements (M e) of ≈2 kg mol −1 for polyethylene, [21] increasing the molecular weight results in a strong increase in the number of entanglements per chain which in turn reduces the solid-state drawability of the fibers. [22] Key to achieving higher draw ratios and processing of higher molecular weights was the reduction of entanglements. The work on polymer solutions by Greassley et al. [20] in the 1970s The rheology, solid state drawability, morphology, and mechanical properties of polyethylene blends containing ultrahigh molecular weight polyethylene (UHMW-PE) and linear-low molecular weight polyethylene waxes (PE wax) are explored. Addition of PE wax enables melt processing of UHMW-PE and improves solid state drawability, providing opportunities in recycling of UHMW-PE waste. Small angle X-ray scattering results show that both PE wax and UHMW-PE align fully in the drawing direction, irrespective whether the PE wax has an M n below or above the critical molecular weight at which entanglements can form (M c). Tensile moduli of drawn specimen are in accordance to the Irvine-Smith model confirming that both UHMW-PE and PE wax align in the drawing direction and no chain slip occurs toward zero strain and both UHMW-PE and PE wax fractions, irrespective of their molecular weight, contribute fully to the modulus. Tensile strength of the blend...